diff --git a/cli/extra_tools/RetrievalAugmentedEmbedder.py b/cli/extra_tools/RAG/RetrievalAugmentedEmbedder.py similarity index 71% rename from cli/extra_tools/RetrievalAugmentedEmbedder.py rename to cli/extra_tools/RAG/RetrievalAugmentedEmbedder.py index c9df821..5203441 100644 --- a/cli/extra_tools/RetrievalAugmentedEmbedder.py +++ b/cli/extra_tools/RAG/RetrievalAugmentedEmbedder.py @@ -172,7 +172,11 @@ def embedding_pipeline(self, url:str) -> None: self.add_function({"signature": func_definition, "embedding": embedding_content}) else: console.log(f"[yellow] Embedding for url {url} exists.") - + + def embedding_pipeline_functions(self): + for i in range(len(self.functions)): + embedding_content = self.functions[i]["embedding"] + self.add_embedding(embedding_content) @staticmethod def cosine_similarity(A: np.ndarray, B: List[np.ndarray]) -> List[float]: @@ -277,58 +281,10 @@ def clear(self) -> None: if __name__ == "__main__": rag = RetrievalAugmentedEmbedder() - urls = [ - "https://docs.scvi-tools.org/en/stable/api/reference/scvi.model.SCVI.html", - "https://docs.scvi-tools.org/en/stable/api/reference/scvi.model.SCANVI.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.calculate_qc_metrics.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.filter_cells.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.filter_genes.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.normalize_total.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.log1p.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.highly_variable_genes.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.regress_out.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.scale.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.pca.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.normalize_pearson_residuals.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.flag_gene_family.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.filter_highly_variable.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.harmony_integrate.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.scrublet.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.scrublet_simulate_doublets.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.neighbors.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.pp.bbknn.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.umap.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.tsne.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.diffmap.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.draw_graph.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.mde.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.embedding_density.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.louvain.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.leiden.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.kmeans.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.score_genes.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.score_genes_cell_cycle.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.tl.rank_genes_groups_logreg.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.get.aggregate.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.get.anndata_to_GPU.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.get.anndata_to_CPU.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.get.X_to_GPU.html", - "https://rapids-singlecell.readthedocs.io/en/latest/api/generated/rapids_singlecell.get.X_to_CPU.html", - - # CellTypist - "https://celltypist.readthedocs.io/en/latest/celltypist.train.html", - "https://celltypist.readthedocs.io/en/latest/celltypist.annotate.html#celltypist.annotate", - "https://celltypist.readthedocs.io/en/latest/celltypist.dotplot.html", - "https://celltypist.readthedocs.io/en/latest/celltypist.models.download_models.html", - "https://celltypist.readthedocs.io/en/latest/celltypist.samples.downsample_adata.html", - "https://celltypist.readthedocs.io/en/latest/celltypist.classifier.AnnotationResult.html", - "https://celltypist.readthedocs.io/en/latest/celltypist.classifier.Classifier.html", - "https://celltypist.readthedocs.io/en/latest/celltypist.models.Model.html", - ] - - for url in urls: - rag.embedding_pipeline(url) - print(rag.query("What is pca")) + #rag.embedding_pipeline_functions() + print(rag.query("Find a function to download the model")) + print(rag.query("AttributeError: module 'celltypist.models' has no attribute 'download_model'")) + rag.cosine_distance_heatmap() diff --git a/cli/extra_tools/RAG/embeddings.jsonl b/cli/extra_tools/RAG/embeddings.jsonl new file mode 100644 index 0000000..a8a09ff --- /dev/null +++ b/cli/extra_tools/RAG/embeddings.jsonl @@ -0,0 +1,44 @@ +[-0.026195848360657692, -0.010568520985543728, -0.0004884175723418593, -0.013966331258416176, 0.04020657762885094, 0.08517905324697495, -0.044839274138212204, 0.011511467397212982, -0.0548718087375164, 0.01506137941032648, -0.04785970225930214, -0.047728266566991806, 0.0463273786008358, -0.00011564424494281411, -0.0275286678224802, -0.031840015202760696, -0.04875560477375984, 0.015580172650516033, -0.08758804947137833, -0.005105928517878056, -0.023666033521294594, -0.054830241948366165, -0.025093067437410355, 0.04295390471816063, -0.06553375720977783, -0.006132333539426327, -0.04332293942570686, -0.08574412018060684, 0.008891614153981209, 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b/cli/extra_tools/RAG/functions.jsonl @@ -0,0 +1,44 @@ +{"signature": "classscvi.model.SCVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,latent_distribution='normal',**kwargs)", "embedding": "Probabilistic VAE for scRNA-seq counts that learns a low-dimensional latent space, corrects batch effects, and models gene expression with (Z)INB/Poisson; provides normalized expression, latent embeddings, and DE utilities. This model is designed for single-cell data and effectively captures biological variability while minimizing technical noise. It supports downstream analyses including clustering, trajectory inference, and differential expression. The latent space representation allows for integration of multiple datasets across batches. Additionally, the framework offers flexible likelihood models and priors for various experimental designs."} +{"signature": "classscvi.model.SCANVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,linear_classifier=False,datamodule=None,**model_kwargs)", "embedding": "Semi-supervised extension of SCVI for label transfer/annotation: learns a label-aware latent space from partially labeled data and trains an integrated classifier (optionally linear) to predict cell types. SCANVI can incorporate known labels while still modeling unlabeled cells. The method improves annotation accuracy by leveraging shared structure in the latent space. It allows flexible classifier options for different prediction tasks. The model is compatible with batch-corrected embeddings and can scale to large single-cell datasets."} +{"signature": "rapids_singlecell.pp.calculate_qc_metrics(adata,*,expr_type='counts',var_type='genes',qc_vars=None,log1p=True,layer=None)", "embedding": "Computes basic QC metrics (e.g., n_genes_by_counts, total_counts, % in gene sets like mitochondria) and writes results to .obs/.var; supports specifying a layer and optional log1p. These metrics help identify low-quality cells or features before downstream analysis. Users can customize which QC variables to include for dataset-specific needs. The function ensures consistent data preprocessing across studies. Outputs are stored directly in the AnnData object for seamless integration with later steps."} +{"signature": "rapids_singlecell.pp.filter_cells(data,*,min_counts=None,min_genes=None,max_counts=None,max_genes=None,inplace=True,verbose=True)", "embedding": "Filters cells by total counts and/or detected genes; removes outliers or returns a filtered copy and records selection masks when inplace=False. This step ensures high-quality cells are retained for analysis. Thresholds can be adjusted to remove extremely low or high-count cells. Users can inspect removed cells for quality assessment. The function integrates cleanly with downstream normalization and feature selection."} +{"signature": "rapids_singlecell.pp.filter_genes(data,*,min_counts=None,min_cells=None,max_counts=None,max_cells=None,inplace=True,verbose=True)", "embedding": "Filters genes by total counts or number of cells expressed; keeps informative genes and drops rarely/overly abundant features. This helps reduce noise and computational burden. Users can set thresholds to retain biologically relevant features. The function maintains consistent gene sets for analysis pipelines. It outputs either a filtered dataset or applies changes in place based on preference."} +{"signature": "rapids_singlecell.pp.normalize_total(adata,*,target_sum=None,layer=None,inplace=True,copy=False)", "embedding": "Library-size normalizes per-cell counts so each cell sums to target_sum (e.g., 1e4); applies to X or a specified layer. Normalization reduces biases from differing sequencing depth. The method prepares data for downstream analyses like PCA and clustering. Users can apply it selectively to layers without affecting raw counts. This step is standard for consistent single-cell data preprocessing."} +{"signature": "rapids_singlecell.pp.log1p(adata,*,layer=None,obsm=None,inplace=True,copy=False)", "embedding": "Applies log1p transformation to expression values in X or a given layer/obsm for variance stabilization prior to HVG/PCA. The transformation reduces skewness in count data. It allows better detection of highly variable genes. The method is compatible with GPU acceleration for large datasets. Log-transformed data improves clustering and visualization quality."} +{"signature": "rapids_singlecell.pp.highly_variable_genes(adata,*,layer=None,min_mean=0.0125,max_mean=3,min_disp=0.5,max_disp=inf,n_top_genes=None,flavor='seurat',n_bins=20,span=0.3,check_values=True,theta=100,clip=None,chunksize=1000,n_samples=10000,batch_key=None)", "embedding": "Identifies highly variable genes (HVGs) using Scanpy/Seurat-style or residual-based methods; supports counts vs log inputs and batch-aware selection. HVGs capture meaningful biological variation. The method can operate across batches for integrated analyses. Users can select top genes for downstream dimensionality reduction. Results are stored in .var for easy filtering and visualization."} +{"signature": "rapids_singlecell.pp.regress_out(adata,keys,*,layer=None,inplace=True,batchsize=None,verbose=False)", "embedding": "Regresses out confounders (e.g., total_counts, pct_counts_mt, cell cycle scores) per gene via linear models to reduce unwanted variation. This ensures that technical effects do not dominate the signal. Users can target specific variables for removal. The method supports batch processing for large datasets. Residuals can be used for downstream PCA or clustering."} +{"signature": "rapids_singlecell.pp.scale(adata,*,zero_center=True,max_value=None,copy=False,layer=None,obsm=None,mask_obs=None,inplace=True)", "embedding": "Standardizes genes to zero mean and unit variance (optionally clipping to max_value); can target X, a layer, or obsm and subset cells via mask. Scaling ensures comparability across genes. Optional clipping prevents extreme values from dominating. The method prepares data for PCA and other algorithms sensitive to variance. Users can apply it selectively to layers or subsets of cells."} +{"signature": "rapids_singlecell.pp.pca(adata,n_comps=None,*,layer=None,zero_center=True,svd_solver=None,random_state=0,mask_var=_empty,use_highly_variable=None,dtype='float32',chunked=False,chunk_size=None,key_added=None,copy=False)", "embedding": "Runs GPU-accelerated PCA (cuML), storing loadings/scores in .varm/.obsm (e.g., 'X_pca'); supports using HVGs and alternative layers. PCA reduces dimensionality for visualization and clustering. The method can operate on selected features for efficiency. GPU acceleration allows large datasets to be processed quickly. Results integrate seamlessly with downstream embedding methods like UMAP."} +{"signature": "rapids_singlecell.pp.normalize_pearson_residuals(adata,*,theta=100,clip=None,check_values=True,layer=None,inplace=True)", "embedding": "Computes analytic Pearson residuals under an NB model for variance normalization (useful for HVG selection and downstream PCA); optional clipping. This method helps stabilize variance across genes with different expression levels. It is particularly effective for preparing data for PCA or clustering. Users can control the clipping threshold to avoid extreme residuals. The resulting normalized data improves the reliability of downstream analyses."} +{"signature": "rapids_singlecell.pp.flag_gene_family(adata,*,gene_family_name,gene_family_prefix=None,gene_list=None)", "embedding": "Adds boolean flags in .var for gene families (e.g., mitochondrial, ribosomal) using a prefix or explicit gene list for easy QC filtering. This allows easy identification of genes belonging to specific functional groups. It supports both automated prefix-based and manual gene-list approaches. The flags are helpful for filtering or annotating genes during preprocessing. It simplifies downstream quality control and analysis workflows."} +{"signature": "rapids_singlecell.pp.filter_highly_variable(adata)", "embedding": "Subsets the AnnData object to genes where .var['highly_variable'] is True; a convenience wrapper after HVG detection. This reduces data dimensionality for faster computation. It ensures downstream analyses focus on informative genes. The method maintains compatibility with all standard AnnData structures. It is commonly used after HVG identification to streamline analysis."} +{"signature": "rapids_singlecell.pp.harmony_integrate(adata,key,*,basis='X_pca',adjusted_basis='X_pca_harmony',dtype=,correction_method='original',use_gemm=False,colsum_algo=None,**kwargs)", "embedding": "Applies Harmony batch correction on a chosen basis (e.g., PCA), writing an adjusted embedding (e.g., 'X_pca_harmony') that mixes batches while preserving structure. This corrects for batch-specific variation in multi-sample datasets. It integrates multiple experiments into a common latent space. The method preserves biological signal while reducing technical noise. Harmony-adjusted embeddings improve clustering and visualization outcomes."} +{"signature": "rapids_singlecell.pp.scrublet(adata,adata_sim=None,*,batch_key=None,sim_doublet_ratio=2.0,expected_doublet_rate=0.05,stdev_doublet_rate=0.02,synthetic_doublet_umi_subsampling=1.0,knn_dist_metric='euclidean',normalize_variance=True,log_transform=False,mean_center=True,n_prin_comps=30,use_approx_neighbors=True,get_doublet_neighbor_parents=False,n_neighbors=None,threshold=None,verbose=True,copy=False,random_state=0)", "embedding": "Runs Scrublet to score and call doublets; writes per-cell doublet scores and predictions, with options for batch-aware processing and neighbor computation. It identifies potential doublet cells that may arise during single-cell capture. Users can adjust thresholds and neighbor parameters for sensitivity. Scrublet outputs help remove confounding doublets from downstream analysis. This ensures higher accuracy in clustering and differential expression studies."} +{"signature": "rapids_singlecell.pp.scrublet_simulate_doublets(adata,*,layer=None,sim_doublet_ratio=2.0,synthetic_doublet_umi_subsampling=1.0,random_seed=0)", "embedding": "Generates synthetic doublets by summing random cell profiles to support Scrublet calibration and thresholding. Synthetic doublets help train the model to distinguish real from artificial doublets. Users can control the simulation ratio and subsampling for flexibility. This step improves doublet detection accuracy. It is a preparatory step for robust quality control in single-cell analysis."} +{"signature": "rapids_singlecell.pp.neighbors(adata,n_neighbors=15,n_pcs=None,*,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),key_added=None,copy=False)", "embedding": "Builds GPU-accelerated KNN graphs (connectivities/distances) from a chosen representation (e.g., PCA); results stored in .obsp and used by UMAP/Leiden. The neighbor graph captures local cell similarities for downstream analysis. Users can specify the number of neighbors and representation type. The output supports visualization and clustering methods. GPU acceleration ensures fast computation on large datasets."} +{"signature": "rapids_singlecell.pp.bbknn(adata,neighbors_within_batch=3,n_pcs=None,*,batch_key=None,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),trim=None,key_added=None,copy=False)", "embedding": "Constructs a batch-balanced KNN graph by drawing neighbors per batch and merging them to reduce batch effects before embedding/clustering. This method ensures fair representation from each batch. It minimizes batch-driven artifacts in clustering. Users can adjust neighbors within batch for flexibility. The graph improves downstream embedding accuracy and integration."} +{"signature": "rapids_singlecell.tl.umap(adata,*,min_dist=0.5,spread=1.0,n_components=2,maxiter=None,alpha=1.0,negative_sample_rate=5,init_pos='auto',random_state=0,a=None,b=None,key_added=None,neighbors_key=None,copy=False)", "embedding": "Computes UMAP embeddings on the neighbor graph using cuML; writes 2D/3D coordinates to .obsm (e.g., 'X_umap'). UMAP preserves local and global structure in low-dimensional space. It is widely used for visualization of single-cell data. Parameters like min_dist and spread control cluster compactness. The method is GPU-accelerated for speed on large datasets."} +{"signature": "rapids_singlecell.tl.tsne(adata,n_pcs=None,*,use_rep=None,perplexity=30,early_exaggeration=12,learning_rate=200,method='barnes_hut',metric='euclidean',key_added=None,copy=False)", "embedding": "Computes t-SNE with GPU acceleration (cuML) from a selected representation; stores coordinates in .obsm (e.g., 'X_tsne'). t-SNE emphasizes local neighborhood relationships for visualization. Perplexity and learning rate can be tuned for cluster resolution. The output is often used alongside UMAP for complementary views. GPU acceleration enables handling of large single-cell datasets efficiently."} +{"signature": "rapids_singlecell.tl.diffmap(adata,n_comps=15,*,neighbors_key=None,sort='decrease',density_normalize=True)", "embedding": "Computes diffusion map components from the neighbor graph for manifold/trajectory structure; stores in .obsm (e.g., 'X_diffmap'). Diffusion maps capture continuous cell transitions. They are useful for trajectory inference and lineage analysis. Users can select the number of components for downstream applications. The method helps reveal developmental or dynamic processes in the data."} +{"signature": "rapids_singlecell.tl.draw_graph(adata,*,init_pos=None,max_iter=500)", "embedding": "Generates a force-directed graph layout (ForceAtlas2 via cuGraph) of the KNN graph for visualization; writes to .obsm (e.g., 'X_draw_graph_fa'). This layout emphasizes neighborhood relationships visually. It is helpful for exploring global structure. Initialization and iteration parameters can be customized. The resulting graph supports interactive visualization and cluster interpretation."} +{"signature": "rapids_singlecell.tl.mde(adata,*,device=None,n_neighbors=15,n_pcs=None,use_rep=None,**kwargs)", "embedding": "Computes a Minimum-Distortion Embedding (MDE) that preserves neighborhood structure; returns a clean visualization alternative to UMAP/t-SNE. MDE emphasizes minimal distortion of distances in low-dimensional space. It provides interpretable visual layouts of cell populations. Users can specify neighbors and representation type. MDE is useful for downstream analysis and comparison of embeddings."} +{"signature": "rapids_singlecell.tl.embedding_density(adata,basis='umap',*,groupby=None,key_added=None,batchsize=10000,components=None)", "embedding": "Estimates local cell density over an existing embedding (e.g., UMAP) and stores per-cell density values for shading/normalization across plots. This allows visualization of dense vs sparse regions. Density estimates can inform cluster interpretation. Users can group cells by metadata for comparison. The method improves visual clarity and downstream analysis insights."} +{"signature": "rapids_singlecell.tl.louvain(adata,resolution=1.0,*,restrict_to=None,key_added='louvain',adjacency=None,n_iterations=100,threshold=1e-07,use_weights=True,neighbors_key=None,obsp=None,dtype=,copy=False)", "embedding": "Runs Louvain community detection (cuGraph) on the neighbor graph; writes cluster labels to .obs[key_added]. Louvain identifies modular structure in single-cell data. Resolution controls the granularity of clusters. Weighted edges and iterations refine clustering stability. The output is widely used for downstream annotation and visualization."} +{"signature": "rapids_singlecell.tl.leiden(adata,resolution=1.0,*,random_state=0,theta=1.0,restrict_to=None,key_added='leiden',adjacency=None,n_iterations=100,use_weights=True,neighbors_key=None,obsp=None,dtype=,copy=False)", "embedding": "Runs Leiden clustering (cuGraph) on the neighbor graph with tunable resolution; outputs labels in .obs[key_added]. Leiden improves on Louvain by guaranteeing well-connected clusters. Resolution affects cluster size and number. Users can control random seed for reproducibility. Clusters are suitable for downstream analysis and visualization."} +{"signature": "rapids_singlecell.tl.kmeans(adata,n_clusters=8,n_pcs=50,*,use_rep='X_pca',n_init=1,random_state=42,key_added='kmeans',copy=False,**kwargs)", "embedding": "Performs K-means on a chosen representation (default PCA) and stores cluster IDs in .obs[key_added]; GPU-accelerated. K-means partitions cells into a fixed number of clusters. Initialization and n_init control clustering stability. The method is suitable for large-scale datasets. Cluster labels can be used for annotation or downstream analysis."} +{"signature": "rapids_singlecell.tl.score_genes(adata,gene_list,*,ctrl_as_ref=True,ctrl_size=50,gene_pool=None,n_bins=25,score_name='score',random_state=0,copy=False,use_raw=None,layer=None)", "embedding": "Computes per-cell signature scores for a gene list using control genes matched by expression bins; writes scores to .obs[score_name]. This method allows quantifying activity of gene sets per cell. Control genes help normalize for expression biases. Scores can be used for visualization, clustering, or differential analysis. The output supports downstream statistical and plotting workflows."} +{"signature": "rapids_singlecell.tl.score_genes_cell_cycle(adata,*,s_genes,g2m_genes,copy=False,**kwargs)", "embedding": "Scores S and G2M phases and assigns cell-cycle phase per cell based on canonical gene sets; stores scores and phase in .obs. This enables identification of proliferating vs quiescent cells. Scores can be used for regression or visualization. Users can provide custom gene sets for different species or experiments. The method aids in removing cell-cycle effects from downstream analysis."} +{"signature": "rapids_singlecell.tl.rank_genes_groups_logreg(adata,groupby,*,groups='all',use_raw=None,reference='rest',n_genes=None,layer=None,**kwds)", "embedding": "Performs one-vs-rest logistic regression DE across groups (e.g., clusters) and writes results to .uns['rank_genes_groups']; GPU-accelerated backend. This identifies marker genes per cluster efficiently. Users can specify reference groups or number of top genes. Results are used for annotation and interpretation. The method is scalable to large single-cell datasets."} +{"signature": "rapids_singlecell.get.aggregate(adata,by,func,*,axis=None,mask=None,dof=1,layer=None,obsm=None,varm=None,return_sparse=False,**kwargs)", "embedding": "Aggregates expression by groups (e.g., mean/sum per cluster, sample, or batch) across obs/var; supports layers/obsm/varm and sparse returns for pseudobulk-like summaries. This provides summarized profiles for downstream analysis. Users can apply custom aggregation functions. Sparse return reduces memory usage for large datasets. The method supports flexible grouping strategies for exploratory or comparative analysis."} +{"signature": "rapids_singlecell.get.anndata_to_GPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Converts AnnData arrays (X/layers/obsm as selected) to GPU (CuPy/cuDF) to enable RAPIDS-accelerated ops; optionally returns a copy. This allows faster computation for large datasets. Users can select which layers or arrays to transfer. The conversion preserves metadata and structure. It is essential for leveraging GPU acceleration in preprocessing and analysis."} +{"signature": "rapids_singlecell.get.anndata_to_CPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Converts AnnData arrays back to CPU (NumPy/SciPy/pandas) from GPU representations; optionally returns a copy. This enables interoperability with standard CPU-based workflows. Users can select specific layers or arrays. Conversion maintains consistency of metadata and data structures. It allows seamless transition between GPU and CPU analyses."} +{"signature": "rapids_singlecell.get.X_to_GPU(X,warning='X')", "embedding": "Utility to convert a numpy/scipy matrix or array to its GPU (CuPy/sparse) equivalent, emitting a contextual warning label if provided. It ensures the data is compatible with RAPIDS GPU operations. The warning helps track which arrays were transferred. Supports dense and sparse formats for flexibility. Conversion accelerates computation on large-scale data."} +{"signature": "rapids_singlecell.get.X_to_CPU(X)", "embedding": "Utility to convert a CuPy/cusparse array back to CPU (NumPy/SciPy) for compatibility with non-GPU workflows. This enables analysis in CPU-only environments. The method preserves data format and structure. Conversion supports both dense and sparse matrices. It allows users to move between GPU and CPU seamlessly."} +{"signature": "celltypist.train(X=None,labels:str|list|tuple|ndarray|Series|Index|None=None,genes:str|list|tuple|ndarray|Series|Index|None=None,transpose_input:bool=False,with_mean:bool=True,check_expression:bool=True,C:float=1.0,solver:str|None=None,max_iter:int|None=None,n_jobs:int|None=None,use_SGD:bool=False,alpha:float=0.0001,use_GPU:bool=False,mini_batch:bool=False,batch_number:int=100,batch_size:int=1000,epochs:int=10,balance_cell_type:bool=False,feature_selection:bool=False,top_genes:int=300,date:str='',details:str='',url:str='',source:str='',version:str='',**kwargs)\u2192Model[source]\uf0c1", "embedding": "Trains a CellTypist logistic-regression classifier (batch/mini-batch options, optional GPU) from expression and labels, returning a portable Model object. It handles preprocessing, feature selection, and scaling internally. The model supports large datasets with mini-batch and GPU acceleration. Training results in a reproducible model for cell-type prediction. The output can be saved, shared, and applied to new datasets."} +{"signature": "celltypist.annotate(filename:AnnData|str='',model:str|Model|None=None,transpose_input:bool=False,gene_file:str|None=None,cell_file:str|None=None,mode:str='bestmatch',p_thres:float=0.5,majority_voting:bool=False,over_clustering:str|list|tuple|ndarray|Series|Index|None=None,use_GPU:bool=False,min_prop:float=0)\u2192AnnotationResult[source]\uf0c1", "embedding": "Applies a pretrained CellTypist model to annotate cells, returning labels and probabilities; supports cluster-level majority voting and optional GPU. It maps expression profiles to known cell types. Probabilities provide confidence scores for each prediction. Majority voting can improve annotation robustness. Results can be used for visualization and downstream analysis."} +{"signature": "celltypist.dotplot(predictions:AnnotationResult,use_as_reference:str|list|tuple|ndarray|Series|Index,use_as_prediction:str='majority_voting',prediction_order:str|list|tuple|ndarray|Series|Index|None=None,reference_order:str|list|tuple|ndarray|Series|Index|None=None,filter_prediction:float=0.0,cmap:str='RdBu_r',vmin:float|None=0.0,vmax:float|None=1.0,colorbar_title:str|None='Meanprobability',dot_min:float|None=0.0,dot_max:float|None=1.0,smallest_dot:float|None=0.0,size_title:str|None='Fractionofcells(%)',swap_axes:bool|None=False,title:str|None='CellTypistlabeltransfer',figsize:tuple|None=None,show:bool|None=None,save:str|bool|None=None,ax:_AxesSubplot|None=None,return_fig:bool|None=False,**kwds)\u2192DotPlot|dict|None[source]\uf0c1", "embedding": "Creates a dot plot comparing reference vs predicted labels from CellTypist, showing mean probabilities (color) and cell fractions (dot size); customizable ordering and display. It visually summarizes the accuracy and confidence of predictions. Axes and orders can be adjusted for clarity. The plot helps identify well-classified vs ambiguous cell types. Dot size and color are informative for interpreting cell-type proportions and certainty."} +{"signature": "celltypist.models.download_models(force_update:bool=False,model:str|list|tuple|None=None)\u2192None[source]\uf0c1", "embedding": "Downloads one or more pretrained CellTypist models (or refreshes them) for local use in annotation and benchmarking. It ensures the latest models are available. Users can select specific models or all models. The method facilitates reproducibility and comparison across studies. Downloaded models are stored locally for fast access during annotation."} +{"signature": "celltypist.samples.downsample_adata(adata:AnnData,mode:str='total',n_cells:int|None=None,by:str|None=None,balance_cell_type:bool=False,random_state:int=0,return_index:bool=True)\u2192AnnData|ndarray[source]\uf0c1", "embedding": "Downsamples an AnnData object by total cells or stratified by a category (e.g., sample/cluster); can return the subset or just selected indices. This allows balancing datasets for analysis or training. Stratification ensures representative sampling across categories. Random seed ensures reproducibility. Downsampling reduces computation time while maintaining biological diversity."} +{"signature": "classcelltypist.classifier.AnnotationResult(labels:DataFrame,decision_mat:DataFrame,prob_mat:DataFrame,adata:AnnData)[source]\uf0c1", "embedding": "Container for CellTypist predictions: per-cell labels, decision/probability matrices, and the associated AnnData; used for plotting and evaluation. It provides structured access to predictions. Probabilities can be analyzed for confidence metrics. Decision matrices allow in-depth interpretation of classification. The container supports integration with downstream analysis pipelines."} +{"signature": "classcelltypist.classifier.Classifier(filename:AnnData|str='',model:Model|str='',transpose:bool=False,gene_file:str|None=None,cell_file:str|None=None)[source]\uf0c1", "embedding": "High-level predictor that loads a CellTypist Model and harmonizes genes/cells to produce annotations; wraps I/O and mapping utilities. It abstracts preprocessing, mapping, and prediction into a single interface. The class supports file and in-memory AnnData inputs. It ensures gene matching and optional transposition. Predictions can be saved or passed."} +{"signature": "classcelltypist.models.Model(clf,scaler,description)[source]\uf0c1", "embedding": "Serialized CellTypist model bundle (classifier + scaler + metadata) used for fast, reproducible cell-type prediction across datasets. The model encapsulates preprocessing steps and learned weights. It allows consistent predictions on new data without retraining. Metadata provides context for model provenance and versioning. The bundle can be saved, shared, and reloaded for reproducible analyses."} diff --git a/cli/extra_tools/embeddings.jsonl b/cli/extra_tools/embeddings.jsonl deleted file mode 100644 index faa609c..0000000 --- a/cli/extra_tools/embeddings.jsonl +++ /dev/null @@ -1,44 +0,0 @@ -[-0.05076559633016586, -0.017743822187185287, -0.010766139253973961, -0.0642252191901207, 0.03709191828966141, 0.06430036574602127, -0.04848451167345047, -0.015592277981340885, -0.043831270188093185, -0.028161345049738884, -0.018403153866529465, -0.08265302330255508, 0.01512408908456564, -0.010527383536100388, -0.04748714342713356, 0.027998873963952065, -0.07361259311437607, 0.035335149616003036, -0.051051437854766846, 0.0006929285009391606, -0.03844114765524864, -0.006479831878095865, -0.04272150620818138, 0.10678649693727493, -0.013279027305543423, 0.009518205188214779, -0.03764968737959862, -0.008123297244310379, 0.000448547798441723, 0.030707476660609245, 0.011373648419976234, 0.023746132850646973, 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89762f6..0000000 --- a/cli/extra_tools/functions.jsonl +++ /dev/null @@ -1,44 +0,0 @@ -{"signature": "classscvi.model.SCVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,latent_distribution='normal',**kwargs)", "embedding": "single-cell Variational Inference[Lopezet al., 2018]."} -{"signature": "classscvi.model.SCANVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,linear_classifier=False,datamodule=None,**model_kwargs)", "embedding": "Single-cell annotation using variational inference[Xuet al., 2021]."} -{"signature": "rapids_singlecell.pp.calculate_qc_metrics(adata,*,expr_type='counts',var_type='genes',qc_vars=None,log1p=True,layer=None)", "embedding": "Calculates basic qc Parameters. Calculates number of genes per cell (n_genes) and number of counts per cell (n_counts).\nLoosely based on calculate_qc_metrics from scanpy [Wolf et al. 2018]. Updatesobsandvarwith columns with qc data."} -{"signature": "rapids_singlecell.pp.filter_cells(data,*,min_counts=None,min_genes=None,max_counts=None,max_genes=None,inplace=True,verbose=True)", "embedding": "Grouping a set of objects by similarity Cluster analysis , or clustering , is a data analysis technique aimed at partitioning a set of objects into groups such that objects within the same group (called a cluster ) exhibit greater similarity to one another (in some specific sense defined by the analyst) than to those in other groups (clusters). It is a main task of exploratory data analysis , and a common technique for statistical data analysis , used in many fields, including pattern recognition , image analysis , information retrieval , bioinformatics , data compression , computer graphics and machine learning . Cluster analysis refers to a family of algorithms and tasks rather than one specific algorithm . It can be achieved by various algorithms that differ significantly in their understanding of what constitutes a cluster and how to efficiently find them. Popular notions of clusters include groups with small distances between cluster members, dense areas of the data space, intervals or particular statistical distributions ."} -{"signature": "rapids_singlecell.pp.filter_genes(data,*,min_counts=None,min_cells=None,max_counts=None,max_cells=None,inplace=True,verbose=True)", "embedding": "Medical condition Sickle cell disease ( SCD ), also simply called sickle cell , is a group of inherited haemoglobin-related blood disorders . The most common type is known as sickle cell anemia . Sickle cell anemia results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells . This leads to the red blood cells adopting an abnormal sickle -like shape under certain circumstances; with this shape, they are unable to deform as they pass through capillaries , causing blockages. Problems in sickle cell disease typically begin around 5 to 6 months of age."} -{"signature": "rapids_singlecell.pp.normalize_total(adata,*,target_sum=None,layer=None,inplace=True,copy=False)", "embedding": "Normalizes rows in matrix so they sum totarget_sum."} -{"signature": "rapids_singlecell.pp.log1p(adata,*,layer=None,obsm=None,inplace=True,copy=False)", "embedding": "Calculated the natural logarithm of one plus the sparse matrix."} -{"signature": "rapids_singlecell.pp.highly_variable_genes(adata,*,layer=None,min_mean=0.0125,max_mean=3,min_disp=0.5,max_disp=inf,n_top_genes=None,flavor='seurat',n_bins=20,span=0.3,check_values=True,theta=100,clip=None,chunksize=1000,n_samples=10000,batch_key=None)", "embedding": "Annotate highly variable genes.\nExpects logarithmized data, except whenflavor='seurat_v3','seurat_v3_paper','pearson_residuals','poisson_gene_selection', in which count data is expected."} -{"signature": "rapids_singlecell.pp.regress_out(adata,keys,*,layer=None,inplace=True,batchsize=None,verbose=False)", "embedding": "Sequence of data points over time Not to be confused with Time (Film and TV) . In mathematics , a time series is a series of data points indexed (or listed or graphed) in time order. Most commonly, a time series is a sequence taken at successive equally spaced points in time. Thus it is a sequence of discrete-time data. Examples of time series are heights of ocean tides , counts of sunspots , and the daily closing value of the Dow Jones Industrial Average ."} -{"signature": "rapids_singlecell.pp.scale(adata,*,zero_center=True,max_value=None,copy=False,layer=None,obsm=None,mask_obs=None,inplace=True)", "embedding": "Machine learning technique In machine learning , attention is a method that determines the importance of each component in a sequence relative to the other components in that sequence. In natural language processing , importance is represented by \"soft\" weights assigned to each word in a sentence. More generally, attention encodes vectors called token embeddings across a fixed-width sequence that can range from tens to millions of tokens in size. Unlike \"hard\" weights, which are computed during the backwards training pass, \"soft\" weights exist only in the forward pass and therefore change with every step of the input. Earlier designs implemented the attention mechanism in a serial recurrent neural network (RNN) language translation system, but a more recent design, namely the transformer , removed the slower sequential RNN and relied more heavily on the faster parallel attention scheme."} -{"signature": "rapids_singlecell.pp.pca(adata,n_comps=None,*,layer=None,zero_center=True,svd_solver=None,random_state=0,mask_var=_empty,use_highly_variable=None,dtype='float32',chunked=False,chunk_size=None,key_added=None,copy=False)", "embedding": "Performs PCA using the cuml decomposition function."} -{"signature": "rapids_singlecell.pp.normalize_pearson_residuals(adata,*,theta=100,clip=None,check_values=True,layer=None,inplace=True)", "embedding": "Applies analytic Pearson residual normalization, based on Lause21.\nThe residuals are based on a negative binomial offset model with overdispersionthetashared across genes. By default, residuals are clipped tosqrt(n_obs)and overdispersiontheta=100is used."} -{"signature": "rapids_singlecell.pp.flag_gene_family(adata,*,gene_family_name,gene_family_prefix=None,gene_list=None)", "embedding": "Flags a gene or gene_family in .var with boolean. (e.g all mitochondrial genes).\nPlease only choose gene_family prefix or gene_list"} -{"signature": "rapids_singlecell.pp.filter_highly_variable(adata)", "embedding": "Filters theAnnDataobject for highly_variable genes. Run highly_varible_genes first."} -{"signature": "rapids_singlecell.pp.harmony_integrate(adata,key,*,basis='X_pca',adjusted_basis='X_pca_harmony',dtype=,correction_method='original',use_gemm=False,colsum_algo=None,**kwargs)", "embedding": "Aspect of music For other uses, see Harmony (disambiguation) . \"Disharmony\" redirects here. For the episode of Angel , see Disharmony ( Angel ) . In music , harmony is the concept of combining different sounds in order to create new, distinct musical ideas. Theories of harmony seek to describe or explain the effects created by distinct pitches or tones coinciding with one another; harmonic objects such as chords , textures and tonalities are identified, defined, and categorized in the development of these theories."} -{"signature": "rapids_singlecell.pp.scrublet(adata,adata_sim=None,*,batch_key=None,sim_doublet_ratio=2.0,expected_doublet_rate=0.05,stdev_doublet_rate=0.02,synthetic_doublet_umi_subsampling=1.0,knn_dist_metric='euclidean',normalize_variance=True,log_transform=False,mean_center=True,n_prin_comps=30,use_approx_neighbors=True,get_doublet_neighbor_parents=False,n_neighbors=None,threshold=None,verbose=True,copy=False,random_state=0)", "embedding": "Predict doublets using Scrublet."} -{"signature": "rapids_singlecell.pp.scrublet_simulate_doublets(adata,*,layer=None,sim_doublet_ratio=2.0,synthetic_doublet_umi_subsampling=1.0,random_seed=0)", "embedding": "Simulate doublets by adding the counts of random observed transcriptome pairs."} -{"signature": "rapids_singlecell.pp.neighbors(adata,n_neighbors=15,n_pcs=None,*,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),key_added=None,copy=False)", "embedding": "Compute a neighborhood graph of observations with cuml."} -{"signature": "rapids_singlecell.pp.bbknn(adata,neighbors_within_batch=3,n_pcs=None,*,batch_key=None,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),trim=None,key_added=None,copy=False)", "embedding": "Batch balanced KNN, altering the KNN procedure to identify each cell\u2019s top neighbours in\neach batch separately instead of the entire cell pool with no accounting for batch.\nThe nearest neighbours for each batch are then merged to create a final list of\nneighbours for the cell."} -{"signature": "rapids_singlecell.tl.umap(adata,*,min_dist=0.5,spread=1.0,n_components=2,maxiter=None,alpha=1.0,negative_sample_rate=5,init_pos='auto',random_state=0,a=None,b=None,key_added=None,neighbors_key=None,copy=False)", "embedding": "Embed the neighborhood graph using UMAP\u2019s cuml implementation."} -{"signature": "rapids_singlecell.tl.tsne(adata,n_pcs=None,*,use_rep=None,perplexity=30,early_exaggeration=12,learning_rate=200,method='barnes_hut',metric='euclidean',key_added=None,copy=False)", "embedding": "Performs t-distributed stochastic neighborhood embedding (tSNE) using cuml library."} -{"signature": "rapids_singlecell.tl.diffmap(adata,n_comps=15,*,neighbors_key=None,sort='decrease',density_normalize=True)", "embedding": "Method of utilizing water in magnetic resonance imaging Medical diagnostic method Diffusion-weighted magnetic resonance imaging ( DWI or DW-MRI ) is the use of specific MRI sequences as well as software that generates images from the resulting data that uses the diffusion of water molecules to generate contrast in MR images. It allows the mapping of the diffusion process of molecules, mainly water, in biological tissues , in vivo and non-invasively. Molecular diffusion in tissues is not random, but reflects interactions with many obstacles, such as macromolecules , fibers, and membranes . Water molecule diffusion patterns can therefore reveal microscopic details about tissue architecture, either normal or in a diseased state. A special kind of DWI, diffusion tensor imaging ( DTI ), has been used extensively to map white matter tractography in the brain."} -{"signature": "rapids_singlecell.tl.draw_graph(adata,*,init_pos=None,max_iter=500)", "embedding": "Force-directed graph drawing with cugraph\u2019s implementation of Force Atlas 2.\nThis is a reimplementation of scanpys function for GPU compute."} -{"signature": "rapids_singlecell.tl.mde(adata,*,device=None,n_neighbors=15,n_pcs=None,use_rep=None,**kwargs)", "embedding": "Util to runpymde.preserve_neighbors()for visualization of single cell embeddings."} -{"signature": "rapids_singlecell.tl.embedding_density(adata,basis='umap',*,groupby=None,key_added=None,batchsize=10000,components=None)", "embedding": "The density matrix embedding theory (DMET) is a numerical technique to solve strongly correlated electronic structure problems. By mapping the system to a fragment plus its entangled quantum bath, the local electron correlation effects on the fragment can be accurately modeled by a post-Hartree\u2013Fock solver. This method has shown high-quality results in 1D- and 2D- Hubbard models , and in chemical model systems incorporating the fully interacting electronic Hamiltonian, including long-range interactions. The basis of DMET is the Schmidt decomposition for quantum states, which shows that a given quantum many-body state, with macroscopically many degrees of freedom, K, can be represented exactly by an Impurity model consisting of 2N degrees of freedom for N<,copy=False)", "embedding": "Class of chemical substance Metal\u2013organic frameworks ( MOFs ) are a class of porous polymers consisting of metal clusters (also known as Secondary Building Units - SBUs) coordinated to organic ligands to form one-, two- or three-dimensional structures. The organic ligands included are sometimes referred to as \"struts\" or \"linkers\", one example being 1,4-benzenedicarboxylic acid (H 2 bdc). MOFs are classified as reticular materials . More formally, a metal\u2013organic framework is a potentially porous extended structure made from metal ions and organic linkers. An extended structure is a structure whose sub-units occur in a constant ratio and are arranged in a repeating pattern."} -{"signature": "rapids_singlecell.tl.leiden(adata,resolution=1.0,*,random_state=0,theta=1.0,restrict_to=None,key_added='leiden',adjacency=None,n_iterations=100,use_weights=True,neighbors_key=None,obsp=None,dtype=,copy=False)", "embedding": "Performs Leiden clustering using cuGraph, which implements the method\ndescribed in:"} -{"signature": "rapids_singlecell.tl.kmeans(adata,n_clusters=8,n_pcs=50,*,use_rep='X_pca',n_init=1,random_state=42,key_added='kmeans',copy=False,**kwargs)", "embedding": "KMeans is a basic but powerful clustering method which is optimized via Expectation Maximization. It randomly selects K data points in X, and computes which samples are close to these points. For every cluster of points, a mean is computed (hence the name), and this becomes the new centroid."} -{"signature": "rapids_singlecell.tl.score_genes(adata,gene_list,*,ctrl_as_ref=True,ctrl_size=50,gene_pool=None,n_bins=25,score_name='score',random_state=0,copy=False,use_raw=None,layer=None)", "embedding": "Bioinformatics method Gene set enrichment analysis (GSEA) (also called functional enrichment analysis or pathway enrichment analysis ) is a method to identify classes of genes or proteins that are over-represented in a large set of genes or proteins, and may have an association with different phenotypes (e.g. different organism growth patterns or diseases). The method uses statistical approaches to identify significantly enriched or depleted groups of genes. Transcriptomics technologies and proteomics results often identify thousands of genes, which are used for the analysis. Researchers performing high-throughput experiments that yield sets of genes (for example, genes that are differentially expressed under different conditions) often want to retrieve a functional profile of that gene set, in order to better understand the underlying biological processes."} -{"signature": "rapids_singlecell.tl.score_genes_cell_cycle(adata,*,s_genes,g2m_genes,copy=False,**kwargs)", "embedding": "Medical condition ZTTK syndrome (Zhu-Tokita-Takenouchi-Kim syndrome) is a rare multisystem disease caused in humans by a genetic mutation of the SON gene . Common symptoms include developmental delay and often light to severe intellectual disability . Characteristic abnormalities include cerebral cortex malformations, vision difficulties, musculoskeletal abnormalities and congenital defects . Individuals with a mutation in the SON gene may not all display these features. However, SON loss of function (LoF) variants appear to cause a clinically distinguished phenotype."} -{"signature": "rapids_singlecell.tl.rank_genes_groups_logreg(adata,groupby,*,groups='all',use_raw=None,reference='rest',n_genes=None,layer=None,**kwds)", "embedding": "Bioinformatics method Gene set enrichment analysis (GSEA) (also called functional enrichment analysis or pathway enrichment analysis ) is a method to identify classes of genes or proteins that are over-represented in a large set of genes or proteins, and may have an association with different phenotypes (e.g. different organism growth patterns or diseases). The method uses statistical approaches to identify significantly enriched or depleted groups of genes. Transcriptomics technologies and proteomics results often identify thousands of genes, which are used for the analysis. Researchers performing high-throughput experiments that yield sets of genes (for example, genes that are differentially expressed under different conditions) often want to retrieve a functional profile of that gene set, in order to better understand the underlying biological processes."} -{"signature": "rapids_singlecell.get.aggregate(adata,by,func,*,axis=None,mask=None,dof=1,layer=None,obsm=None,varm=None,return_sparse=False,**kwargs)", "embedding": "Data visualization technique \"Colormap\" redirects here. For indexed palettes, see Indexed color . A heat map (or heatmap ) is a 2-dimensional data visualization technique that represents the magnitude of individual values within a dataset as a color. The variation in color may be by hue or intensity . In some applications such as crime analytics or website click-tracking, color is used to represent the density of data points rather than a value associated with each point."} -{"signature": "rapids_singlecell.get.anndata_to_GPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Parallel computing platform and programming model For other uses, see CUDA (disambiguation) . CUDA , which stands for Compute Unified Device Architecture , is a proprietary parallel computing platform and application programming interface (API) that allows software to use certain types of graphics processing units (GPUs) for accelerated general-purpose processing, significantly broadening their utility in scientific and high-performance computing . CUDA was created by Nvidia starting in 2004 and was officially released by in 2007. When it was first introduced, the name was an acronym for Compute Unified Device Architecture , but Nvidia later dropped the common use of the acronym and now rarely expands it. CUDA is both a software layer that manages data, giving direct access to the GPU and CPU as necessary, and a library of APIs that enable parallel computation for various needs."} -{"signature": "rapids_singlecell.get.anndata_to_CPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Parallel computing platform and programming model For other uses, see CUDA (disambiguation) . CUDA , which stands for Compute Unified Device Architecture , is a proprietary parallel computing platform and application programming interface (API) that allows software to use certain types of graphics processing units (GPUs) for accelerated general-purpose processing, significantly broadening their utility in scientific and high-performance computing . CUDA was created by Nvidia starting in 2004 and was officially released by in 2007. When it was first introduced, the name was an acronym for Compute Unified Device Architecture , but Nvidia later dropped the common use of the acronym and now rarely expands it. CUDA is both a software layer that manages data, giving direct access to the GPU and CPU as necessary, and a library of APIs that enable parallel computation for various needs."} -{"signature": "rapids_singlecell.get.X_to_GPU(X,warning='X')", "embedding": "Parallel computing platform and programming model For other uses, see CUDA (disambiguation) . CUDA , which stands for Compute Unified Device Architecture , is a proprietary parallel computing platform and application programming interface (API) that allows software to use certain types of graphics processing units (GPUs) for accelerated general-purpose processing, significantly broadening their utility in scientific and high-performance computing . CUDA was created by Nvidia starting in 2004 and was officially released by in 2007. When it was first introduced, the name was an acronym for Compute Unified Device Architecture , but Nvidia later dropped the common use of the acronym and now rarely expands it. CUDA is both a software layer that manages data, giving direct access to the GPU and CPU as necessary, and a library of APIs that enable parallel computation for various needs."} -{"signature": "rapids_singlecell.get.X_to_CPU(X)", "embedding": "Parallel computing platform and programming model For other uses, see CUDA (disambiguation) . CUDA , which stands for Compute Unified Device Architecture , is a proprietary parallel computing platform and application programming interface (API) that allows software to use certain types of graphics processing units (GPUs) for accelerated general-purpose processing, significantly broadening their utility in scientific and high-performance computing . CUDA was created by Nvidia starting in 2004 and was officially released by in 2007. When it was first introduced, the name was an acronym for Compute Unified Device Architecture , but Nvidia later dropped the common use of the acronym and now rarely expands it. CUDA is both a software layer that manages data, giving direct access to the GPU and CPU as necessary, and a library of APIs that enable parallel computation for various needs."} -{"signature": "celltypist.train(X=None,labels:str|list|tuple|ndarray|Series|Index|None=None,genes:str|list|tuple|ndarray|Series|Index|None=None,transpose_input:bool=False,with_mean:bool=True,check_expression:bool=True,C:float=1.0,solver:str|None=None,max_iter:int|None=None,n_jobs:int|None=None,use_SGD:bool=False,alpha:float=0.0001,use_GPU:bool=False,mini_batch:bool=False,batch_number:int=100,batch_size:int=1000,epochs:int=10,balance_cell_type:bool=False,feature_selection:bool=False,top_genes:int=300,date:str='',details:str='',url:str='',source:str='',version:str='',**kwargs)\u2192Model[source]\uf0c1", "embedding": "Train a celltypist model using mini-batch (optional) logistic classifier with a global solver or stochastic gradient descent (SGD) learning."} -{"signature": "celltypist.annotate(filename:AnnData|str='',model:str|Model|None=None,transpose_input:bool=False,gene_file:str|None=None,cell_file:str|None=None,mode:str='bestmatch',p_thres:float=0.5,majority_voting:bool=False,over_clustering:str|list|tuple|ndarray|Series|Index|None=None,use_GPU:bool=False,min_prop:float=0)\u2192AnnotationResult[source]\uf0c1", "embedding": "Suite of advanced driver-assistance system features Tesla Autopilot is an advanced driver-assistance system (ADAS) developed by Tesla, Inc. that provides partial vehicle automation, corresponding to Level 2 automation as defined by SAE International . All Tesla vehicles produced after April 2019 include Autopilot, which features autosteer and traffic-aware cruise control . Customers can purchase or subscribe to an optional package called \"Full Self-Driving (Supervised)\", also known as \"FSD\", which adds features such as semi-autonomous navigation, response to traffic lights and stop signs, lane change assistance , self-parking , and the ability to summon the car from a parking space. Since 2013, Tesla CEO Elon Musk has repeatedly predicted that the company would achieve fully autonomous driving (SAE Level 5 ) within one to three years, but these goals have not been met."} -{"signature": "celltypist.dotplot(predictions:AnnotationResult,use_as_reference:str|list|tuple|ndarray|Series|Index,use_as_prediction:str='majority_voting',prediction_order:str|list|tuple|ndarray|Series|Index|None=None,reference_order:str|list|tuple|ndarray|Series|Index|None=None,filter_prediction:float=0.0,cmap:str='RdBu_r',vmin:float|None=0.0,vmax:float|None=1.0,colorbar_title:str|None='Meanprobability',dot_min:float|None=0.0,dot_max:float|None=1.0,smallest_dot:float|None=0.0,size_title:str|None='Fractionofcells(%)',swap_axes:bool|None=False,title:str|None='CellTypistlabeltransfer',figsize:tuple|None=None,show:bool|None=None,save:str|bool|None=None,ax:_AxesSubplot|None=None,return_fig:bool|None=False,**kwds)\u2192DotPlot|dict|None[source]\uf0c1", "embedding": "Generate a dot plot showing CellTypist label transfer. This is a wrapper around thescanpy.pl.DotPlotwith selected parameters and customized defaults."} -{"signature": "celltypist.models.download_models(force_update:bool=False,model:str|list|tuple|None=None)\u2192None[source]\uf0c1", "embedding": "Large language model by Meta AI Not to be confused with LaMDA . Llama ( Large Language Model Meta AI ) is a family of large language models (LLMs) released by Meta AI starting in February 2023. The latest version is Llama 4, released in April 2025. Llama models come in different sizes, ranging from 1 billion to 2 trillion parameters. Initially only a foundation model , starting with Llama 2, Meta AI released instruction fine-tuned versions alongside foundation models."} -{"signature": "celltypist.samples.downsample_adata(adata:AnnData,mode:str='total',n_cells:int|None=None,by:str|None=None,balance_cell_type:bool=False,random_state:int=0,return_index:bool=True)\u2192AnnData|ndarray[source]\uf0c1", "embedding": "Type of artificial neural network A convolutional neural network ( CNN ) is a type of feedforward neural network that learns features via filter (or kernel ) optimization. This type of deep learning network has been applied to process and make predictions from many different types of data including text, images and audio. Convolution-based networks are the de-facto standard in deep learning -based approaches to computer vision and image processing, and have only recently been replaced\u2014in some cases\u2014by newer deep learning architectures such as the transformer . Vanishing gradients and exploding gradients, seen during backpropagation in earlier neural networks, are prevented by the regularization that comes from using shared weights over fewer connections. For example, for each neuron in the fully-connected layer, 10,000 weights would be required for processing an image sized 100 \u00d7 100 pixels."} -{"signature": "classcelltypist.classifier.AnnotationResult(labels:DataFrame,decision_mat:DataFrame,prob_mat:DataFrame,adata:AnnData)[source]\uf0c1", "embedding": "Buddhist term for the six senses In Buddhism , \u0101yatana ( P\u0101li ; Sanskrit : \u0906\u092f\u0924\u0928) is a \"center of experience\" or \"mental home,\" which create one's experience. The term (P\u0101li; Skt. ) refers to six cognitive functions, namely sight, hearing, smelling, tasting, body-cognition, and mind-cognition. \u0100yatana may refer to both ordinary experience and the chain of processes leading to bondage, as to awakened experience centered in detachment and meditative accomplishment. The Buddhist path aims to relocate one from the ordinary, sensual centers of experience to the \"mental home\" of the purified, liberated awareness of the jhanas."} -{"signature": "classcelltypist.classifier.Classifier(filename:AnnData|str='',model:Model|str='',transpose:bool=False,gene_file:str|None=None,cell_file:str|None=None)[source]\uf0c1", "embedding": "Bases:object"} -{"signature": "classcelltypist.models.Model(clf,scaler,description)[source]\uf0c1", "embedding": "Bases:object"} diff --git a/cli/olaf/src/olaf/agents/AgentSystem.py b/cli/olaf/src/olaf/agents/AgentSystem.py index 064a84a..0d5a0f5 100644 --- a/cli/olaf/src/olaf/agents/AgentSystem.py +++ b/cli/olaf/src/olaf/agents/AgentSystem.py @@ -52,10 +52,10 @@ def get_full_prompt(self, global_policy=None) -> str: full_prompt += "\n\n**YOU MUST USE THESE EXACT COMMANDS TO DELEGATE TASKS. NO OTHER FORMATTING OR COMMANDS ARE ALLOWED.**" if self.is_rag_enabled: - full_prompt += "\n\nYou can query your specialized knowledge base for more context with the following command:" + full_prompt += "\n\nIf an error occurs, admit the error and query your specialized knowledge base for more context with the following command:" full_prompt += f"\n- Command: `query_rag_`" full_prompt += f"\n - Description: Retrieves relevant information about a specific from your knowledge base. Replace with a concise, descriptive search query (e.g., function names, task you are trying to complete)." - full_prompt += f"\n - Example: `query_rag_`" + full_prompt += f"\n - Example: `query_rag_scvi model setup`" if self.code_samples: full_prompt += "\n\n - Code Samples Available:" @@ -159,4 +159,4 @@ def get_instructions(self) -> str: return instructions def __repr__(self) -> str: - return f"AgentSystem(global_policy='{self.global_policy[:40]}...', agents={list(self.agents.keys())})" \ No newline at end of file + return f"AgentSystem(global_policy='{self.global_policy[:40]}...', agents={list(self.agents.keys())})" diff --git a/cli/olaf/src/olaf/agents/integration_system.json b/cli/olaf/src/olaf/agents/integration_system.json index 50bc252..4d53f2c 100644 --- a/cli/olaf/src/olaf/agents/integration_system.json +++ b/cli/olaf/src/olaf/agents/integration_system.json @@ -50,4 +50,4 @@ } } } -} \ No newline at end of file +} diff --git a/cli/olaf/src/olaf/cli/run_cli.py b/cli/olaf/src/olaf/cli/run_cli.py index 88d27ab..34966ea 100644 --- a/cli/olaf/src/olaf/cli/run_cli.py +++ b/cli/olaf/src/olaf/cli/run_cli.py @@ -11,13 +11,6 @@ from rich.prompt import Prompt, IntPrompt from dotenv import load_dotenv -from olaf.config import DEFAULT_AGENT_DIR, ENV_FILE -from olaf.agents.AgentSystem import Agent, AgentSystem -from olaf.core.io_helpers import collect_resources -from olaf.core.sandbox_management import (init_docker, init_singularity_exec) -from olaf.execution.runner import run_agent_session, SandboxManager -from olaf.datasets.czi_datasets import get_datasets_dir - PACKAGE_ROOT = Path(__file__).resolve().parent.parent PACKAGE_AGENTS_DIR = PACKAGE_ROOT / "agents" PACKAGE_DATASETS_DIR = PACKAGE_ROOT / "datasets" @@ -56,7 +49,7 @@ def _prompt_for_file( choice_str = Prompt.ask("Enter the number of your choice", choices=[str(i) for i in range(1, len(found_files) + 1)]) return found_files[int(choice_str) - 1]['path'] -def _prompt_for_driver(console: Console, system: AgentSystem) -> str: +def _prompt_for_driver(console: Console, system: 'AgentSystem') -> str: """Prompts the user to select a driver agent from the loaded system.""" console.print("[bold]Select a driver agent:[/bold]") agents = list(system.agents.keys()) @@ -97,11 +90,11 @@ def _prompt_for_benchmark_module(console: Console) -> Optional[Path]: class AppContext: def __init__(self): self.console = Console() - self.agent_system: AgentSystem | None = None + self.agent_system: 'AgentSystem' | None = None self.driver_agent_name: str | None = None self.roster_instructions: str | None = None self.analysis_context: str | None = None - self.sandbox_manager: SandboxManager | None = None + self.sandbox_manager: 'SandboxManager' | None = None self.llm_client: object | None = None self.initial_history: List[dict] | None = None self.dataset_path: Path | None = None @@ -122,6 +115,13 @@ def main_run_callback( sandbox: str = typer.Option(None, "--sandbox", help="Sandbox backend to use: 'docker' or 'singularity'."), force_refresh: bool = typer.Option(False, "--force-refresh", help="Force refresh/rebuild of the sandbox environment."), ): + # --- Heavy imports are deferred to here --- + from olaf.config import DEFAULT_AGENT_DIR, ENV_FILE + from olaf.agents.AgentSystem import AgentSystem + from olaf.core.io_helpers import collect_resources + from olaf.core.sandbox_management import init_docker, init_singularity_exec + from olaf.datasets.czi_datasets import get_datasets_dir + load_dotenv(dotenv_path=ENV_FILE) app_context = AppContext() console = app_context.console @@ -194,6 +194,10 @@ def main_run_callback( def _setup_and_run_session(context: AppContext, history: list, is_auto: bool, max_turns: int, benchmark_modules: Optional[List[Path]] = None): """Helper to start, run, and stop the sandbox session.""" + # --- Heavy imports needed for the session are deferred to here --- + from olaf.execution.runner import run_agent_session, SandboxManager + from olaf.agents.AgentSystem import AgentSystem + sandbox_manager = cast(SandboxManager, context.sandbox_manager) console = context.console diff --git a/cli/olaf/src/olaf/execution/runner.py b/cli/olaf/src/olaf/execution/runner.py index 20b4ab3..171dd5d 100644 --- a/cli/olaf/src/olaf/execution/runner.py +++ b/cli/olaf/src/olaf/execution/runner.py @@ -40,7 +40,7 @@ def exec_code(self, code: str, timeout: int) -> dict: _OUTPUTS_DIR = OLAF_HOME / "runs" _SNIPPET_DIR = _OUTPUTS_DIR / "snippets" _LEDGER_PATH = _OUTPUTS_DIR / f"benchmark_history_{datetime.utcnow().strftime('%Y%m%d-%H%M%S')}.jsonl" -_RAG_RE = re.compile(r"query_rag_<([^>]+)>") +_RAG_RE = re.compile(r"query_rag_([^>]+)") RAG = RetrievalAugmentedGeneration() @@ -241,33 +241,33 @@ def run_agent_session( stderr = exec_result.get('stderr', '') if stderr and current_agent.is_rag_enabled: func_error_patterns = [ - r"missing \d+ required positional argument", # TypeError: missing argument - r"NameError: name '(\w+)' is not defined", # NameError - r"AttributeError: '.*' object has no attribute '(\w+)'", # missing attribute - r"got an unexpected keyword argument" # wrong keyword argument - ] + r"(\w+)\(.*\) missing \d+ required positional argument", # TypeError missing arguments + r"NameError: name '(\w+)' is not defined", # NameError + r"AttributeError: .* has no attribute '(\w+)'", # AttributeError + r"'(\w+)\(.*\) got an unexpected keyword argument" # Unexpected keyword argument + ] + function_name = "" retrieved_docs = "" - if any(re.search(pat, stderr) for pat in func_error_patterns): - lines = stderr.strip().splitlines() - if len(lines) >= 2: - code_line = lines[-2].strip() # second-to-last line: code that failed - match = re.search(r'(\w+)\s*\(', code_line) - if match: - function_name = match.group(1) - + + for pat in func_error_patterns: + match = re.search(pat, stderr) + if match: + function_name = [g for g in match.groups() if g] + break + if function_name: + function_name = function_name[0] + console.print(f"[yellow]🔍 Incorrect function signature detected: {function_name}, function database search...[/yellow]") retrieved_docs = RAG.retrieve_function(function_name) - console.print(f"[yellow]🔍 Missing function detected: {function_name}, function database search...[/yellow]") - if retrieved_docs: - console.print(f"[green] Query successful - Function signature found. [/green]") - feedback += f"\n {function_name} produced an error. The correct function signature for {function_name} is:\n{retrieved_docs}" - console.print(feedback) - history.append({"role": "system", "content": feedback}) - continue - else: - print(f"RAG Error Query unsuccessful - Function signature does not exist in the current database.") - + if retrieved_docs: + console.print(f"[green] Query successful - Function signature found. [/green]") + feedback += f"\n {function_name} produced an error. The correct function signature for {function_name} is:\n{retrieved_docs}" + history.append({"role": "system", "content": feedback}) + continue + else: + print(f"Error Query unsuccessful - Function signature does not exist in the current database.") + if is_auto: if benchmark_modules: @@ -302,4 +302,4 @@ def run_agent_session( if user_input: history.append({"role": "user", "content": user_input}) display(console, "user", user_input) - break \ No newline at end of file + break diff --git a/cli/olaf/src/olaf/rag/RetrievalAugmentedGeneration.py b/cli/olaf/src/olaf/rag/RetrievalAugmentedGeneration.py index 10f7765..46df8f0 100644 --- a/cli/olaf/src/olaf/rag/RetrievalAugmentedGeneration.py +++ b/cli/olaf/src/olaf/rag/RetrievalAugmentedGeneration.py @@ -25,6 +25,7 @@ RAG_DIR = Path(__file__).resolve().parent.parent / "rag" EMBEDDING_FILE = RAG_DIR / "embeddings.jsonl" FUNCTIONS_FILE = RAG_DIR / "functions.jsonl" +MIN_SIMILARITY = 0.7 class RetrievalAugmentedGeneration(): model = SentenceTransformer("Qwen/Qwen3-Embedding-0.6B") @@ -75,10 +76,13 @@ def query(self, text_query: str) -> Optional[np.ndarray]: query_embedding = self.model.encode([text_query])[0] sims = self.cosine_similarity(query_embedding, self.embeddings) idx = np.argmax(sims) + if sims[idx] < MIN_SIMILARITY: + return None return self.functions[idx]["signature"] # ──────Implementation────────────────────────────────────────────────────────── if __name__ == "__main__": rag = RetrievalAugmentedGeneration() - print(rag.query("What is pca")) + print(rag.query("Find a function to download model")) + print(rag.query("AttributeError: module 'celltypist.models' has no attribute 'download_model'")) diff --git a/cli/olaf/src/olaf/rag/embeddings.jsonl b/cli/olaf/src/olaf/rag/embeddings.jsonl index faa609c..a8a09ff 100644 --- a/cli/olaf/src/olaf/rag/embeddings.jsonl +++ b/cli/olaf/src/olaf/rag/embeddings.jsonl @@ -1,44 +1,44 @@ -[-0.05076559633016586, -0.017743822187185287, -0.010766139253973961, 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0.03598936274647713, 0.005269113462418318, 0.03755499795079231, -0.016351109370589256, -0.02328590862452984, 0.018302949145436287, -0.004402142483741045, -0.004138467367738485, 0.02309967577457428, -0.021443048492074013, 0.05533153936266899, 0.006691140588372946, 0.007385250646620989, 0.02309543825685978, 0.03541326895356178, 0.026528483256697655, -0.057800281792879105, 0.005820502992719412, 0.04586648568511009, -0.019826145842671394, -0.008179794065654278, -0.00556462537497282, -0.019851204007864, -0.0031257010996341705, -0.03530190512537956, 0.027438567951321602, 0.03724319487810135, 0.009999454952776432, -0.022144915536046028, -0.053668271750211716, 0.027301272377371788, 0.0045426334254443645, -0.013081426732242107, 0.005951325874775648, 0.005645062308758497, 0.024571118876338005, 0.027728430926799774, 0.014608311466872692, 0.0027097302954643965, 0.0559709407389164, 0.003731060540303588, 0.009709416888654232, 0.009154131636023521, 0.01944395899772644, 0.024163397029042244, 0.02518489956855774, 0.010521071963012218, -0.03990719094872475, -0.032502107322216034, 0.037427935749292374, 0.003572222776710987] diff --git a/cli/olaf/src/olaf/rag/functions.jsonl b/cli/olaf/src/olaf/rag/functions.jsonl index 1bc5c67..6199563 100644 --- a/cli/olaf/src/olaf/rag/functions.jsonl +++ b/cli/olaf/src/olaf/rag/functions.jsonl @@ -1,44 +1,44 @@ -{"signature": "classscvi.model.SCVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,latent_distribution='normal',**kwargs)", "embedding": "Probabilistic VAE for scRNA-seq counts that learns a low-dimensional latent space, corrects batch effects, and models gene expression with (Z)INB/Poisson; provides normalized expression, latent embeddings, and DE utilities."} -{"signature": "classscvi.model.SCANVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,linear_classifier=False,datamodule=None,**model_kwargs)", "embedding": "Semi-supervised extension of SCVI for label transfer/annotation: learns a label-aware latent space from partially labeled data and trains an integrated classifier (optionally linear) to predict cell types."} -{"signature": "rapids_singlecell.pp.calculate_qc_metrics(adata,*,expr_type='counts',var_type='genes',qc_vars=None,log1p=True,layer=None)", "embedding": "Computes basic QC metrics (e.g., n_genes_by_counts, total_counts, % in gene sets like mitochondria) and writes results to .obs/.var; supports specifying a layer and optional log1p."} -{"signature": "rapids_singlecell.pp.filter_cells(data,*,min_counts=None,min_genes=None,max_counts=None,max_genes=None,inplace=True,verbose=True)", "embedding": "Filters cells by total counts and/or detected genes; removes outliers or returns a filtered copy and records selection masks when inplace=False."} -{"signature": "rapids_singlecell.pp.filter_genes(data,*,min_counts=None,min_cells=None,max_counts=None,max_cells=None,inplace=True,verbose=True)", "embedding": "Filters genes by total counts or number of cells expressed; keeps informative genes and drops rarely/overly abundant features."} -{"signature": "rapids_singlecell.pp.normalize_total(adata,*,target_sum=None,layer=None,inplace=True,copy=False)", "embedding": "Library-size normalizes per-cell counts so each cell sums to target_sum (e.g., 1e4); applies to X or a specified layer."} -{"signature": "rapids_singlecell.pp.log1p(adata,*,layer=None,obsm=None,inplace=True,copy=False)", "embedding": "Applies log1p transformation to expression values in X or a given layer/obsm for variance stabilization prior to HVG/PCA."} -{"signature": "rapids_singlecell.pp.highly_variable_genes(adata,*,layer=None,min_mean=0.0125,max_mean=3,min_disp=0.5,max_disp=inf,n_top_genes=None,flavor='seurat',n_bins=20,span=0.3,check_values=True,theta=100,clip=None,chunksize=1000,n_samples=10000,batch_key=None)", "embedding": "Identifies highly variable genes (HVGs) using Scanpy/Seurat-style or residual-based methods; supports counts vs log inputs and batch-aware selection."} -{"signature": "rapids_singlecell.pp.regress_out(adata,keys,*,layer=None,inplace=True,batchsize=None,verbose=False)", "embedding": "Regresses out confounders (e.g., total_counts, pct_counts_mt, cell cycle scores) per gene via linear models to reduce unwanted variation."} -{"signature": "rapids_singlecell.pp.scale(adata,*,zero_center=True,max_value=None,copy=False,layer=None,obsm=None,mask_obs=None,inplace=True)", "embedding": "Standardizes genes to zero mean and unit variance (optionally clipping to max_value); can target X, a layer, or obsm and subset cells via mask."} -{"signature": "rapids_singlecell.pp.pca(adata,n_comps=None,*,layer=None,zero_center=True,svd_solver=None,random_state=0,mask_var=_empty,use_highly_variable=None,dtype='float32',chunked=False,chunk_size=None,key_added=None,copy=False)", "embedding": "Runs GPU-accelerated PCA (cuML), storing loadings/scores in .varm/.obsm (e.g., 'X_pca'); supports using HVGs and alternative layers."} -{"signature": "rapids_singlecell.pp.normalize_pearson_residuals(adata,*,theta=100,clip=None,check_values=True,layer=None,inplace=True)", "embedding": "Computes analytic Pearson residuals under an NB model for variance normalization (useful for HVG selection and downstream PCA); optional clipping."} -{"signature": "rapids_singlecell.pp.flag_gene_family(adata,*,gene_family_name,gene_family_prefix=None,gene_list=None)", "embedding": "Adds boolean flags in .var for gene families (e.g., mitochondrial, ribosomal) using a prefix or explicit gene list for easy QC filtering."} -{"signature": "rapids_singlecell.pp.filter_highly_variable(adata)", "embedding": "Subsets the AnnData object to genes where .var['highly_variable'] is True; a convenience wrapper after HVG detection."} -{"signature": "rapids_singlecell.pp.harmony_integrate(adata,key,*,basis='X_pca',adjusted_basis='X_pca_harmony',dtype=,correction_method='original',use_gemm=False,colsum_algo=None,**kwargs)", "embedding": "Applies Harmony batch correction on a chosen basis (e.g., PCA), writing an adjusted embedding (e.g., 'X_pca_harmony') that mixes batches while preserving structure."} -{"signature": "rapids_singlecell.pp.scrublet(adata,adata_sim=None,*,batch_key=None,sim_doublet_ratio=2.0,expected_doublet_rate=0.05,stdev_doublet_rate=0.02,synthetic_doublet_umi_subsampling=1.0,knn_dist_metric='euclidean',normalize_variance=True,log_transform=False,mean_center=True,n_prin_comps=30,use_approx_neighbors=True,get_doublet_neighbor_parents=False,n_neighbors=None,threshold=None,verbose=True,copy=False,random_state=0)", "embedding": "Runs Scrublet to score and call doublets; writes per-cell doublet scores and predictions, with options for batch-aware processing and neighbor computation."} -{"signature": "rapids_singlecell.pp.scrublet_simulate_doublets(adata,*,layer=None,sim_doublet_ratio=2.0,synthetic_doublet_umi_subsampling=1.0,random_seed=0)", "embedding": "Generates synthetic doublets by summing random cell profiles to support Scrublet calibration and thresholding."} -{"signature": "rapids_singlecell.pp.neighbors(adata,n_neighbors=15,n_pcs=None,*,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),key_added=None,copy=False)", "embedding": "Builds GPU-accelerated KNN graphs (connectivities/distances) from a chosen representation (e.g., PCA); results stored in .obsp and used by UMAP/Leiden."} -{"signature": "rapids_singlecell.pp.bbknn(adata,neighbors_within_batch=3,n_pcs=None,*,batch_key=None,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),trim=None,key_added=None,copy=False)", "embedding": "Constructs a batch-balanced KNN graph by drawing neighbors per batch and merging them to reduce batch effects before embedding/clustering."} -{"signature": "rapids_singlecell.tl.umap(adata,*,min_dist=0.5,spread=1.0,n_components=2,maxiter=None,alpha=1.0,negative_sample_rate=5,init_pos='auto',random_state=0,a=None,b=None,key_added=None,neighbors_key=None,copy=False)", "embedding": "Computes UMAP embeddings on the neighbor graph using cuML; writes 2D/3D coordinates to .obsm (e.g., 'X_umap')."} -{"signature": "rapids_singlecell.tl.tsne(adata,n_pcs=None,*,use_rep=None,perplexity=30,early_exaggeration=12,learning_rate=200,method='barnes_hut',metric='euclidean',key_added=None,copy=False)", "embedding": "Computes t-SNE with GPU acceleration (cuML) from a selected representation; stores coordinates in .obsm (e.g., 'X_tsne')."} -{"signature": "rapids_singlecell.tl.diffmap(adata,n_comps=15,*,neighbors_key=None,sort='decrease',density_normalize=True)", "embedding": "Computes diffusion map components from the neighbor graph for manifold/trajectory structure; stores in .obsm (e.g., 'X_diffmap')."} -{"signature": "rapids_singlecell.tl.draw_graph(adata,*,init_pos=None,max_iter=500)", "embedding": "Generates a force-directed graph layout (ForceAtlas2 via cuGraph) of the KNN graph for visualization; writes to .obsm (e.g., 'X_draw_graph_fa')."} -{"signature": "rapids_singlecell.tl.mde(adata,*,device=None,n_neighbors=15,n_pcs=None,use_rep=None,**kwargs)", "embedding": "Computes a Minimum-Distortion Embedding (MDE) that preserves neighborhood structure; returns a clean visualization alternative to UMAP/t-SNE."} -{"signature": "rapids_singlecell.tl.embedding_density(adata,basis='umap',*,groupby=None,key_added=None,batchsize=10000,components=None)", "embedding": "Estimates local cell density over an existing embedding (e.g., UMAP) and stores per-cell density values for shading/normalization across plots."} -{"signature": "rapids_singlecell.tl.louvain(adata,resolution=1.0,*,restrict_to=None,key_added='louvain',adjacency=None,n_iterations=100,threshold=1e-07,use_weights=True,neighbors_key=None,obsp=None,dtype=,copy=False)", "embedding": "Runs Louvain community detection (cuGraph) on the neighbor graph; writes cluster labels to .obs[key_added]."} -{"signature": "rapids_singlecell.tl.leiden(adata,resolution=1.0,*,random_state=0,theta=1.0,restrict_to=None,key_added='leiden',adjacency=None,n_iterations=100,use_weights=True,neighbors_key=None,obsp=None,dtype=,copy=False)", "embedding": "Runs Leiden clustering (cuGraph) on the neighbor graph with tunable resolution; outputs labels in .obs[key_added]."} -{"signature": "rapids_singlecell.tl.kmeans(adata,n_clusters=8,n_pcs=50,*,use_rep='X_pca',n_init=1,random_state=42,key_added='kmeans',copy=False,**kwargs)", "embedding": "Performs K-means on a chosen representation (default PCA) and stores cluster IDs in .obs[key_added]; GPU-accelerated."} -{"signature": "rapids_singlecell.tl.score_genes(adata,gene_list,*,ctrl_as_ref=True,ctrl_size=50,gene_pool=None,n_bins=25,score_name='score',random_state=0,copy=False,use_raw=None,layer=None)", "embedding": "Computes per-cell signature scores for a gene list using control genes matched by expression bins; writes scores to .obs[score_name]."} -{"signature": "rapids_singlecell.tl.score_genes_cell_cycle(adata,*,s_genes,g2m_genes,copy=False,**kwargs)", "embedding": "Scores S and G2M phases and assigns cell-cycle phase per cell based on canonical gene sets; stores scores and phase in .obs."} -{"signature": "rapids_singlecell.tl.rank_genes_groups_logreg(adata,groupby,*,groups='all',use_raw=None,reference='rest',n_genes=None,layer=None,**kwds)", "embedding": "Performs one-vs-rest logistic regression DE across groups (e.g., clusters) and writes results to .uns['rank_genes_groups']; GPU-accelerated backend."} -{"signature": "rapids_singlecell.get.aggregate(adata,by,func,*,axis=None,mask=None,dof=1,layer=None,obsm=None,varm=None,return_sparse=False,**kwargs)", "embedding": "Aggregates expression by groups (e.g., mean/sum per cluster, sample, or batch) across obs/var; supports layers/obsm/varm and sparse returns for pseudobulk-like summaries."} -{"signature": "rapids_singlecell.get.anndata_to_GPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Converts AnnData arrays (X/layers/obsm as selected) to GPU (CuPy/cuDF) to enable RAPIDS-accelerated ops; optionally returns a copy."} -{"signature": "rapids_singlecell.get.anndata_to_CPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Converts AnnData arrays back to CPU (NumPy/SciPy/pandas) from GPU representations; optionally returns a copy."} -{"signature": "rapids_singlecell.get.X_to_GPU(X,warning='X')", "embedding": "Utility to convert a numpy/scipy matrix or array to its GPU (CuPy/sparse) equivalent, emitting a contextual warning label if provided."} -{"signature": "rapids_singlecell.get.X_to_CPU(X)", "embedding": "Utility to convert a CuPy/cusparse array back to CPU (NumPy/SciPy) for compatibility with non-GPU workflows."} -{"signature": "celltypist.train(X=None,labels:str|list|tuple|ndarray|Series|Index|None=None,genes:str|list|tuple|ndarray|Series|Index|None=None,transpose_input:bool=False,with_mean:bool=True,check_expression:bool=True,C:float=1.0,solver:str|None=None,max_iter:int|None=None,n_jobs:int|None=None,use_SGD:bool=False,alpha:float=0.0001,use_GPU:bool=False,mini_batch:bool=False,batch_number:int=100,batch_size:int=1000,epochs:int=10,balance_cell_type:bool=False,feature_selection:bool=False,top_genes:int=300,date:str='',details:str='',url:str='',source:str='',version:str='',**kwargs)\u2192Model[source]\uf0c1", "embedding": "Trains a CellTypist logistic-regression classifier (batch/mini-batch options, optional GPU) from expression and labels, returning a portable Model object."} -{"signature": "celltypist.annotate(filename:AnnData|str='',model:str|Model|None=None,transpose_input:bool=False,gene_file:str|None=None,cell_file:str|None=None,mode:str='bestmatch',p_thres:float=0.5,majority_voting:bool=False,over_clustering:str|list|tuple|ndarray|Series|Index|None=None,use_GPU:bool=False,min_prop:float=0)\u2192AnnotationResult[source]\uf0c1", "embedding": "Applies a pretrained CellTypist model to annotate cells, returning labels and probabilities; supports cluster-level majority voting and optional GPU."} -{"signature": "celltypist.dotplot(predictions:AnnotationResult,use_as_reference:str|list|tuple|ndarray|Series|Index,use_as_prediction:str='majority_voting',prediction_order:str|list|tuple|ndarray|Series|Index|None=None,reference_order:str|list|tuple|ndarray|Series|Index|None=None,filter_prediction:float=0.0,cmap:str='RdBu_r',vmin:float|None=0.0,vmax:float|None=1.0,colorbar_title:str|None='Meanprobability',dot_min:float|None=0.0,dot_max:float|None=1.0,smallest_dot:float|None=0.0,size_title:str|None='Fractionofcells(%)',swap_axes:bool|None=False,title:str|None='CellTypistlabeltransfer',figsize:tuple|None=None,show:bool|None=None,save:str|bool|None=None,ax:_AxesSubplot|None=None,return_fig:bool|None=False,**kwds)\u2192DotPlot|dict|None[source]\uf0c1", "embedding": "Creates a dot plot comparing reference vs predicted labels from CellTypist, showing mean probabilities (color) and cell fractions (dot size); customizable ordering and display."} -{"signature": "celltypist.models.download_models(force_update:bool=False,model:str|list|tuple|None=None)\u2192None[source]\uf0c1", "embedding": "Downloads one or more pretrained CellTypist models (or refreshes them) for local use in annotation and benchmarking."} -{"signature": "celltypist.samples.downsample_adata(adata:AnnData,mode:str='total',n_cells:int|None=None,by:str|None=None,balance_cell_type:bool=False,random_state:int=0,return_index:bool=True)\u2192AnnData|ndarray[source]\uf0c1", "embedding": "Downsamples an AnnData object by total cells or stratified by a category (e.g., sample/cluster); can return the subset or just selected indices."} -{"signature": "classcelltypist.classifier.AnnotationResult(labels:DataFrame,decision_mat:DataFrame,prob_mat:DataFrame,adata:AnnData)[source]\uf0c1", "embedding": "Container for CellTypist predictions: per-cell labels, decision/probability matrices, and the associated AnnData; used for plotting and evaluation."} -{"signature": "classcelltypist.classifier.Classifier(filename:AnnData|str='',model:Model|str='',transpose:bool=False,gene_file:str|None=None,cell_file:str|None=None)[source]\uf0c1", "embedding": "High-level predictor that loads a CellTypist Model and harmonizes genes/cells to produce annotations; wraps I/O and mapping utilities."} -{"signature": "classcelltypist.models.Model(clf,scaler,description)[source]\uf0c1", "embedding": "Serialized CellTypist model bundle (classifier + scaler + metadata) used for fast, reproducible cell-type prediction across datasets."} +{"signature": "classscvi.model.SCVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,latent_distribution='normal',**kwargs)", "embedding": "Probabilistic VAE for scRNA-seq counts that learns a low-dimensional latent space, corrects batch effects, and models gene expression with (Z)INB/Poisson; provides normalized expression, latent embeddings, and DE utilities. This model is designed for single-cell data and effectively captures biological variability while minimizing technical noise. It supports downstream analyses including clustering, trajectory inference, and differential expression. The latent space representation allows for integration of multiple datasets across batches. Additionally, the framework offers flexible likelihood models and priors for various experimental designs."} +{"signature": "classscvi.model.SCANVI(adata=None,registry=None,n_hidden=128,n_latent=10,n_layers=1,dropout_rate=0.1,dispersion='gene',gene_likelihood='zinb',use_observed_lib_size=True,linear_classifier=False,datamodule=None,**model_kwargs)", "embedding": "Semi-supervised extension of SCVI for label transfer/annotation: learns a label-aware latent space from partially labeled data and trains an integrated classifier (optionally linear) to predict cell types. SCANVI can incorporate known labels while still modeling unlabeled cells. The method improves annotation accuracy by leveraging shared structure in the latent space. It allows flexible classifier options for different prediction tasks. The model is compatible with batch-corrected embeddings and can scale to large single-cell datasets."} +{"signature": "rapids_singlecell.pp.calculate_qc_metrics(adata,*,expr_type='counts',var_type='genes',qc_vars=None,log1p=True,layer=None)", "embedding": "Computes basic QC metrics (e.g., n_genes_by_counts, total_counts, % in gene sets like mitochondria) and writes results to .obs/.var; supports specifying a layer and optional log1p. These metrics help identify low-quality cells or features before downstream analysis. Users can customize which QC variables to include for dataset-specific needs. The function ensures consistent data preprocessing across studies. Outputs are stored directly in the AnnData object for seamless integration with later steps."} +{"signature": "rapids_singlecell.pp.filter_cells(data,*,min_counts=None,min_genes=None,max_counts=None,max_genes=None,inplace=True,verbose=True)", "embedding": "Filters cells by total counts and/or detected genes; removes outliers or returns a filtered copy and records selection masks when inplace=False. This step ensures high-quality cells are retained for analysis. Thresholds can be adjusted to remove extremely low or high-count cells. Users can inspect removed cells for quality assessment. The function integrates cleanly with downstream normalization and feature selection."} +{"signature": "rapids_singlecell.pp.filter_genes(data,*,min_counts=None,min_cells=None,max_counts=None,max_cells=None,inplace=True,verbose=True)", "embedding": "Filters genes by total counts or number of cells expressed; keeps informative genes and drops rarely/overly abundant features. This helps reduce noise and computational burden. Users can set thresholds to retain biologically relevant features. The function maintains consistent gene sets for analysis pipelines. It outputs either a filtered dataset or applies changes in place based on preference."} +{"signature": "rapids_singlecell.pp.normalize_total(adata,*,target_sum=None,layer=None,inplace=True,copy=False)", "embedding": "Library-size normalizes per-cell counts so each cell sums to target_sum (e.g., 1e4); applies to X or a specified layer. Normalization reduces biases from differing sequencing depth. The method prepares data for downstream analyses like PCA and clustering. Users can apply it selectively to layers without affecting raw counts. This step is standard for consistent single-cell data preprocessing."} +{"signature": "rapids_singlecell.pp.log1p(adata,*,layer=None,obsm=None,inplace=True,copy=False)", "embedding": "Applies log1p transformation to expression values in X or a given layer/obsm for variance stabilization prior to HVG/PCA. The transformation reduces skewness in count data. It allows better detection of highly variable genes. The method is compatible with GPU acceleration for large datasets. Log-transformed data improves clustering and visualization quality."} +{"signature": "rapids_singlecell.pp.highly_variable_genes(adata,*,layer=None,min_mean=0.0125,max_mean=3,min_disp=0.5,max_disp=inf,n_top_genes=None,flavor='seurat',n_bins=20,span=0.3,check_values=True,theta=100,clip=None,chunksize=1000,n_samples=10000,batch_key=None)", "embedding": "Identifies highly variable genes (HVGs) using Scanpy/Seurat-style or residual-based methods; supports counts vs log inputs and batch-aware selection. HVGs capture meaningful biological variation. The method can operate across batches for integrated analyses. Users can select top genes for downstream dimensionality reduction. Results are stored in .var for easy filtering and visualization."} +{"signature": "rapids_singlecell.pp.regress_out(adata,keys,*,layer=None,inplace=True,batchsize=None,verbose=False)", "embedding": "Regresses out confounders (e.g., total_counts, pct_counts_mt, cell cycle scores) per gene via linear models to reduce unwanted variation. This ensures that technical effects do not dominate the signal. Users can target specific variables for removal. The method supports batch processing for large datasets. Residuals can be used for downstream PCA or clustering."} +{"signature": "rapids_singlecell.pp.scale(adata,*,zero_center=True,max_value=None,copy=False,layer=None,obsm=None,mask_obs=None,inplace=True)", "embedding": "Standardizes genes to zero mean and unit variance (optionally clipping to max_value); can target X, a layer, or obsm and subset cells via mask. Scaling ensures comparability across genes. Optional clipping prevents extreme values from dominating. The method prepares data for PCA and other algorithms sensitive to variance. Users can apply it selectively to layers or subsets of cells."} +{"signature": "rapids_singlecell.pp.pca(adata,n_comps=None,*,layer=None,zero_center=True,svd_solver=None,random_state=0,mask_var=_empty,use_highly_variable=None,dtype='float32',chunked=False,chunk_size=None,key_added=None,copy=False)", "embedding": "Runs GPU-accelerated PCA (cuML), storing loadings/scores in .varm/.obsm (e.g., 'X_pca'); supports using HVGs and alternative layers. PCA reduces dimensionality for visualization and clustering. The method can operate on selected features for efficiency. GPU acceleration allows large datasets to be processed quickly. Results integrate seamlessly with downstream embedding methods like UMAP."} +{"signature": "rapids_singlecell.pp.normalize_pearson_residuals(adata,*,theta=100,clip=None,check_values=True,layer=None,inplace=True)", "embedding": "Computes analytic Pearson residuals under an NB model for variance normalization (useful for HVG selection and downstream PCA); optional clipping. This method helps stabilize variance across genes with different expression levels. It is particularly effective for preparing data for PCA or clustering. Users can control the clipping threshold to avoid extreme residuals. The resulting normalized data improves the reliability of downstream analyses."} +{"signature": "rapids_singlecell.pp.flag_gene_family(adata,*,gene_family_name,gene_family_prefix=None,gene_list=None)", "embedding": "Adds boolean flags in .var for gene families (e.g., mitochondrial, ribosomal) using a prefix or explicit gene list for easy QC filtering. This allows easy identification of genes belonging to specific functional groups. It supports both automated prefix-based and manual gene-list approaches. The flags are helpful for filtering or annotating genes during preprocessing. It simplifies downstream quality control and analysis workflows."} +{"signature": "rapids_singlecell.pp.filter_highly_variable(adata)", "embedding": "Subsets the AnnData object to genes where .var['highly_variable'] is True; a convenience wrapper after HVG detection. This reduces data dimensionality for faster computation. It ensures downstream analyses focus on informative genes. The method maintains compatibility with all standard AnnData structures. It is commonly used after HVG identification to streamline analysis."} +{"signature": "rapids_singlecell.pp.harmony_integrate(adata,key,*,basis='X_pca',adjusted_basis='X_pca_harmony',dtype=,correction_method='original',use_gemm=False,colsum_algo=None,**kwargs)", "embedding": "Applies Harmony batch correction on a chosen basis (e.g., PCA), writing an adjusted embedding (e.g., 'X_pca_harmony') that mixes batches while preserving structure. This corrects for batch-specific variation in multi-sample datasets. It integrates multiple experiments into a common latent space. The method preserves biological signal while reducing technical noise. Harmony-adjusted embeddings improve clustering and visualization outcomes."} +{"signature": "rapids_singlecell.pp.scrublet(adata,adata_sim=None,*,batch_key=None,sim_doublet_ratio=2.0,expected_doublet_rate=0.05,stdev_doublet_rate=0.02,synthetic_doublet_umi_subsampling=1.0,knn_dist_metric='euclidean',normalize_variance=True,log_transform=False,mean_center=True,n_prin_comps=30,use_approx_neighbors=True,get_doublet_neighbor_parents=False,n_neighbors=None,threshold=None,verbose=True,copy=False,random_state=0)", "embedding": "Runs Scrublet to score and call doublets; writes per-cell doublet scores and predictions, with options for batch-aware processing and neighbor computation. It identifies potential doublet cells that may arise during single-cell capture. Users can adjust thresholds and neighbor parameters for sensitivity. Scrublet outputs help remove confounding doublets from downstream analysis. This ensures higher accuracy in clustering and differential expression studies."} +{"signature": "rapids_singlecell.pp.scrublet_simulate_doublets(adata,*,layer=None,sim_doublet_ratio=2.0,synthetic_doublet_umi_subsampling=1.0,random_seed=0)", "embedding": "Generates synthetic doublets by summing random cell profiles to support Scrublet calibration and thresholding. Synthetic doublets help train the model to distinguish real from artificial doublets. Users can control the simulation ratio and subsampling for flexibility. This step improves doublet detection accuracy. It is a preparatory step for robust quality control in single-cell analysis."} +{"signature": "rapids_singlecell.pp.neighbors(adata,n_neighbors=15,n_pcs=None,*,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),key_added=None,copy=False)", "embedding": "Builds GPU-accelerated KNN graphs (connectivities/distances) from a chosen representation (e.g., PCA); results stored in .obsp and used by UMAP/Leiden. The neighbor graph captures local cell similarities for downstream analysis. Users can specify the number of neighbors and representation type. The output supports visualization and clustering methods. GPU acceleration ensures fast computation on large datasets."} +{"signature": "rapids_singlecell.pp.bbknn(adata,neighbors_within_batch=3,n_pcs=None,*,batch_key=None,use_rep=None,random_state=0,algorithm='brute',metric='euclidean',metric_kwds=mappingproxy({}),algorithm_kwds=mappingproxy({}),trim=None,key_added=None,copy=False)", "embedding": "Constructs a batch-balanced KNN graph by drawing neighbors per batch and merging them to reduce batch effects before embedding/clustering. This method ensures fair representation from each batch. It minimizes batch-driven artifacts in clustering. Users can adjust neighbors within batch for flexibility. The graph improves downstream embedding accuracy and integration."} +{"signature": "rapids_singlecell.tl.umap(adata,*,min_dist=0.5,spread=1.0,n_components=2,maxiter=None,alpha=1.0,negative_sample_rate=5,init_pos='auto',random_state=0,a=None,b=None,key_added=None,neighbors_key=None,copy=False)", "embedding": "Computes UMAP embeddings on the neighbor graph using cuML; writes 2D/3D coordinates to .obsm (e.g., 'X_umap'). UMAP preserves local and global structure in low-dimensional space. It is widely used for visualization of single-cell data. Parameters like min_dist and spread control cluster compactness. The method is GPU-accelerated for speed on large datasets."} +{"signature": "rapids_singlecell.tl.tsne(adata,n_pcs=None,*,use_rep=None,perplexity=30,early_exaggeration=12,learning_rate=200,method='barnes_hut',metric='euclidean',key_added=None,copy=False)", "embedding": "Computes t-SNE with GPU acceleration (cuML) from a selected representation; stores coordinates in .obsm (e.g., 'X_tsne'). t-SNE emphasizes local neighborhood relationships for visualization. Perplexity and learning rate can be tuned for cluster resolution. The output is often used alongside UMAP for complementary views. GPU acceleration enables handling of large single-cell datasets efficiently."} +{"signature": "rapids_singlecell.tl.diffmap(adata,n_comps=15,*,neighbors_key=None,sort='decrease',density_normalize=True)", "embedding": "Computes diffusion map components from the neighbor graph for manifold/trajectory structure; stores in .obsm (e.g., 'X_diffmap'). Diffusion maps capture continuous cell transitions. They are useful for trajectory inference and lineage analysis. Users can select the number of components for downstream applications. The method helps reveal developmental or dynamic processes in the data."} +{"signature": "rapids_singlecell.tl.draw_graph(adata,*,init_pos=None,max_iter=500)", "embedding": "Generates a force-directed graph layout (ForceAtlas2 via cuGraph) of the KNN graph for visualization; writes to .obsm (e.g., 'X_draw_graph_fa'). This layout emphasizes neighborhood relationships visually. It is helpful for exploring global structure. Initialization and iteration parameters can be customized. The resulting graph supports interactive visualization and cluster interpretation."} +{"signature": "rapids_singlecell.tl.mde(adata,*,device=None,n_neighbors=15,n_pcs=None,use_rep=None,**kwargs)", "embedding": "Computes a Minimum-Distortion Embedding (MDE) that preserves neighborhood structure; returns a clean visualization alternative to UMAP/t-SNE. MDE emphasizes minimal distortion of distances in low-dimensional space. It provides interpretable visual layouts of cell populations. Users can specify neighbors and representation type. MDE is useful for downstream analysis and comparison of embeddings."} +{"signature": "rapids_singlecell.tl.embedding_density(adata,basis='umap',*,groupby=None,key_added=None,batchsize=10000,components=None)", "embedding": "Estimates local cell density over an existing embedding (e.g., UMAP) and stores per-cell density values for shading/normalization across plots. This allows visualization of dense vs sparse regions. Density estimates can inform cluster interpretation. Users can group cells by metadata for comparison. The method improves visual clarity and downstream analysis insights."} +{"signature": "rapids_singlecell.tl.louvain(adata,resolution=1.0,*,restrict_to=None,key_added='louvain',adjacency=None,n_iterations=100,threshold=1e-07,use_weights=True,neighbors_key=None,obsp=None,dtype=,copy=False)", "embedding": "Runs Louvain community detection (cuGraph) on the neighbor graph; writes cluster labels to .obs[key_added]. Louvain identifies modular structure in single-cell data. Resolution controls the granularity of clusters. Weighted edges and iterations refine clustering stability. The output is widely used for downstream annotation and visualization."} +{"signature": "rapids_singlecell.tl.leiden(adata,resolution=1.0,*,random_state=0,theta=1.0,restrict_to=None,key_added='leiden',adjacency=None,n_iterations=100,use_weights=True,neighbors_key=None,obsp=None,dtype=,copy=False)", "embedding": "Runs Leiden clustering (cuGraph) on the neighbor graph with tunable resolution; outputs labels in .obs[key_added]. Leiden improves on Louvain by guaranteeing well-connected clusters. Resolution affects cluster size and number. Users can control random seed for reproducibility. Clusters are suitable for downstream analysis and visualization."} +{"signature": "rapids_singlecell.tl.kmeans(adata,n_clusters=8,n_pcs=50,*,use_rep='X_pca',n_init=1,random_state=42,key_added='kmeans',copy=False,**kwargs)", "embedding": "Performs K-means on a chosen representation (default PCA) and stores cluster IDs in .obs[key_added]; GPU-accelerated. K-means partitions cells into a fixed number of clusters. Initialization and n_init control clustering stability. The method is suitable for large-scale datasets. Cluster labels can be used for annotation or downstream analysis."} +{"signature": "rapids_singlecell.tl.score_genes(adata,gene_list,*,ctrl_as_ref=True,ctrl_size=50,gene_pool=None,n_bins=25,score_name='score',random_state=0,copy=False,use_raw=None,layer=None)", "embedding": "Computes per-cell signature scores for a gene list using control genes matched by expression bins; writes scores to .obs[score_name]. This method allows quantifying activity of gene sets per cell. Control genes help normalize for expression biases. Scores can be used for visualization, clustering, or differential analysis. The output supports downstream statistical and plotting workflows."} +{"signature": "rapids_singlecell.tl.score_genes_cell_cycle(adata,*,s_genes,g2m_genes,copy=False,**kwargs)", "embedding": "Scores S and G2M phases and assigns cell-cycle phase per cell based on canonical gene sets; stores scores and phase in .obs. This enables identification of proliferating vs quiescent cells. Scores can be used for regression or visualization. Users can provide custom gene sets for different species or experiments. The method aids in removing cell-cycle effects from downstream analysis."} +{"signature": "rapids_singlecell.tl.rank_genes_groups_logreg(adata,groupby,*,groups='all',use_raw=None,reference='rest',n_genes=None,layer=None,**kwds)", "embedding": "Performs one-vs-rest logistic regression DE across groups (e.g., clusters) and writes results to .uns['rank_genes_groups']; GPU-accelerated backend. This identifies marker genes per cluster efficiently. Users can specify reference groups or number of top genes. Results are used for annotation and interpretation. The method is scalable to large single-cell datasets."} +{"signature": "rapids_singlecell.get.aggregate(adata,by,func,*,axis=None,mask=None,dof=1,layer=None,obsm=None,varm=None,return_sparse=False,**kwargs)", "embedding": "Aggregates expression by groups (e.g., mean/sum per cluster, sample, or batch) across obs/var; supports layers/obsm/varm and sparse returns for pseudobulk-like summaries. This provides summarized profiles for downstream analysis. Users can apply custom aggregation functions. Sparse return reduces memory usage for large datasets. The method supports flexible grouping strategies for exploratory or comparative analysis."} +{"signature": "rapids_singlecell.get.anndata_to_GPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Converts AnnData arrays (X/layers/obsm as selected) to GPU (CuPy/cuDF) to enable RAPIDS-accelerated ops; optionally returns a copy. This allows faster computation for large datasets. Users can select which layers or arrays to transfer. The conversion preserves metadata and structure. It is essential for leveraging GPU acceleration in preprocessing and analysis."} +{"signature": "rapids_singlecell.get.anndata_to_CPU(adata,layer=None,convert_all=False,copy=False)", "embedding": "Converts AnnData arrays back to CPU (NumPy/SciPy/pandas) from GPU representations; optionally returns a copy. This enables interoperability with standard CPU-based workflows. Users can select specific layers or arrays. Conversion maintains consistency of metadata and data structures. It allows seamless transition between GPU and CPU analyses."} +{"signature": "rapids_singlecell.get.X_to_GPU(X,warning='X')", "embedding": "Utility to convert a numpy/scipy matrix or array to its GPU (CuPy/sparse) equivalent, emitting a contextual warning label if provided. It ensures the data is compatible with RAPIDS GPU operations. The warning helps track which arrays were transferred. Supports dense and sparse formats for flexibility. Conversion accelerates computation on large-scale data."} +{"signature": "rapids_singlecell.get.X_to_CPU(X)", "embedding": "Utility to convert a CuPy/cusparse array back to CPU (NumPy/SciPy) for compatibility with non-GPU workflows. This enables analysis in CPU-only environments. The method preserves data format and structure. Conversion supports both dense and sparse matrices. It allows users to move between GPU and CPU seamlessly."} +{"signature": "celltypist.train(X=None,labels:str|list|tuple|ndarray|Series|Index|None=None,genes:str|list|tuple|ndarray|Series|Index|None=None,transpose_input:bool=False,with_mean:bool=True,check_expression:bool=True,C:float=1.0,solver:str|None=None,max_iter:int|None=None,n_jobs:int|None=None,use_SGD:bool=False,alpha:float=0.0001,use_GPU:bool=False,mini_batch:bool=False,batch_number:int=100,batch_size:int=1000,epochs:int=10,balance_cell_type:bool=False,feature_selection:bool=False,top_genes:int=300,date:str='',details:str='',url:str='',source:str='',version:str='',**kwargs)\u2192Model[source]\uf0c1", "embedding": "Trains a CellTypist logistic-regression classifier (batch/mini-batch options, optional GPU) from expression and labels, returning a portable Model object. It handles preprocessing, feature selection, and scaling internally. The model supports large datasets with mini-batch and GPU acceleration. Training results in a reproducible model for cell-type prediction. The output can be saved, shared, and applied to new datasets."} +{"signature": "celltypist.annotate(filename:AnnData|str='',model:str|Model|None=None,transpose_input:bool=False,gene_file:str|None=None,cell_file:str|None=None,mode:str='bestmatch',p_thres:float=0.5,majority_voting:bool=False,over_clustering:str|list|tuple|ndarray|Series|Index|None=None,use_GPU:bool=False,min_prop:float=0)\u2192AnnotationResult[source]\uf0c1", "embedding": "Applies a pretrained CellTypist model to annotate cells, returning labels and probabilities; supports cluster-level majority voting and optional GPU. It maps expression profiles to known cell types. Probabilities provide confidence scores for each prediction. Majority voting can improve annotation robustness. Results can be used for visualization and downstream analysis."} +{"signature": "celltypist.dotplot(predictions:AnnotationResult,use_as_reference:str|list|tuple|ndarray|Series|Index,use_as_prediction:str='majority_voting',prediction_order:str|list|tuple|ndarray|Series|Index|None=None,reference_order:str|list|tuple|ndarray|Series|Index|None=None,filter_prediction:float=0.0,cmap:str='RdBu_r',vmin:float|None=0.0,vmax:float|None=1.0,colorbar_title:str|None='Meanprobability',dot_min:float|None=0.0,dot_max:float|None=1.0,smallest_dot:float|None=0.0,size_title:str|None='Fractionofcells(%)',swap_axes:bool|None=False,title:str|None='CellTypistlabeltransfer',figsize:tuple|None=None,show:bool|None=None,save:str|bool|None=None,ax:_AxesSubplot|None=None,return_fig:bool|None=False,**kwds)\u2192DotPlot|dict|None[source]\uf0c1", "embedding": "Creates a dot plot comparing reference vs predicted labels from CellTypist, showing mean probabilities (color) and cell fractions (dot size); customizable ordering and display. It visually summarizes the accuracy and confidence of predictions. Axes and orders can be adjusted for clarity. The plot helps identify well-classified vs ambiguous cell types. Dot size and color are informative for interpreting cell-type proportions and certainty."} +{"signature": "celltypist.models.download_models(force_update:bool=False,model:str|list|tuple|None=None)\u2192None[source]\uf0c1", "embedding": "Downloads one or more pretrained CellTypist models (or refreshes them) for local use in annotation and benchmarking. It ensures the latest models are available. Users can select specific models or all models. The method facilitates reproducibility and comparison across studies. Downloaded models are stored locally for fast access during annotation."} +{"signature": "celltypist.samples.downsample_adata(adata:AnnData,mode:str='total',n_cells:int|None=None,by:str|None=None,balance_cell_type:bool=False,random_state:int=0,return_index:bool=True)\u2192AnnData|ndarray[source]\uf0c1", "embedding": "Downsamples an AnnData object by total cells or stratified by a category (e.g., sample/cluster); can return the subset or just selected indices. This allows balancing datasets for analysis or training. Stratification ensures representative sampling across categories. Random seed ensures reproducibility. Downsampling reduces computation time while maintaining biological diversity."} +{"signature": "classcelltypist.classifier.AnnotationResult(labels:DataFrame,decision_mat:DataFrame,prob_mat:DataFrame,adata:AnnData)[source]\uf0c1", "embedding": "Container for CellTypist predictions: per-cell labels, decision/probability matrices, and the associated AnnData; used for plotting and evaluation. It provides structured access to predictions. Probabilities can be analyzed for confidence metrics. Decision matrices allow in-depth interpretation of classification. The container supports integration with downstream analysis pipelines."} +{"signature": "classcelltypist.classifier.Classifier(filename:AnnData|str='',model:Model|str='',transpose:bool=False,gene_file:str|None=None,cell_file:str|None=None)[source]\uf0c1", "embedding": "High-level predictor that loads a CellTypist Model and harmonizes genes/cells to produce annotations; wraps I/O and mapping utilities. It abstracts preprocessing, mapping, and prediction into a single interface. The class supports file and in-memory AnnData inputs. It ensures gene matching and optional transposition. Predictions can be saved or passed."} +{"signature": "classcelltypist.models.Model(clf,scaler,description)[source]\uf0c1", "embedding": "Serialized CellTypist model bundle (classifier + scaler + metadata) used for fast, reproducible cell-type prediction across datasets. The model encapsulates preprocessing steps and learned weights. It allows consistent predictions on new data without retraining. Metadata provides context for model provenance and versioning. The bundle can be saved, shared, and reloaded for reproducible analyses."}