Workflow to analyze targeted immunoglobulin sequencing data for patient-specific immunoproteogenomics
Python >= 3.8 Singularity >= 3.6 Snakemake >= 5.24.0
# optional, if that's how you set up the env
source ~/venvs/[my_Python38_sing36_sm524_env]/bin/activate
# clone wf repository
git clone https://github.com/heuselm/igseq_workflow.git
# descend into wf directory
cd igseq_workflow
# stage input data
copy/move fastq_R1.gz and fastq_R2.gz to 00_input/
define sample_id, master_barcode, slave_barcode, species in header-less, tab-separated barcodes.txt in 00_input/
# run
run ./run.sh