diff --git a/salmon_library_types.md b/salmon_library_types.md
new file mode 100644
index 0000000..69d6483
--- /dev/null
+++ b/salmon_library_types.md
@@ -0,0 +1,155 @@
+# Salmon Library Type: ISR vs Auto Mode
+
+## Overview
+
+Salmon and related tools (alevin, alevin-fry, piscem) use library type specifications to understand the orientation and strandedness of sequencing reads. This is critical for accurate quantification in RNA-seq experiments.
+
+## Library Type Format
+
+In salmon, library types follow the format: `<STRANDEDNESS><ORIENTATION><DIRECTION>`
+
+For single-cell RNA-seq with alevin/simpleaf, the commonly used parameter is `--expected-ori` which simplifies this specification.
+
+## ISR Mode (Inward Stranded Reverse)
+
+**ISR** stands for **Inward, Stranded, Reverse-complement**.
+
+### Characteristics:
+- **I (Inward)**: Paired-end reads face inward toward each other (most common for Illumina paired-end sequencing)
+- **S (Stranded)**: The library is strand-specific (preserves information about which DNA strand was transcribed)
+- **R (Reverse)**: The first read (R1) comes from the reverse complement of the transcript
+
+### Behavior:
+- Salmon explicitly expects reads to match the ISR orientation pattern
+- Reads that don't match this pattern may be incorrectly quantified or discarded
+- This is the standard for many stranded RNA-seq protocols including:
+  - Illumina TruSeq Stranded mRNA
+  - 10x Chromium single-cell RNA-seq (uses `fw` which is equivalent for single-end barcode reads)
+  - dUTP-based stranded protocols
+
+### Use Case:
+Use ISR when you **know** your library is stranded and follows the reverse-complement orientation. This provides:
+- ✅ More accurate quantification
+- ✅ Strand-specific information
+- ✅ Better handling of overlapping genes on opposite strands
+- ❌ Incorrect results if library prep doesn't match
+
+## Auto Mode (Automatic Detection)
+
+**Auto** (or **A**) enables automatic library type detection.
+
+### Characteristics:
+- Salmon examines a subset of reads at the beginning of quantification
+- Infers the most likely library type from the actual data
+- Falls back to the most probable orientation if uncertain
+
+### Behavior:
+- Analyzes the first ~5 million reads (configurable)
+- Tests different orientation patterns to find the best match
+- Reports the detected library type in the output
+- Can handle mixed or uncertain library preparations
+
+### Use Case:
+Use auto mode when:
+- ✅ Library type is unknown or uncertain
+- ✅ Testing new protocols or library prep methods
+- ✅ Working with data from external sources
+- ✅ Prefer robustness over strict assumptions
+- ❌ Slightly slower than explicit mode (due to detection phase)
+- ⚠️ May incorrectly detect type with low-quality or unusual data
+
+## Key Differences Summary
+
+| Aspect | ISR Mode | Auto Mode |
+|--------|----------|-----------|
+| **Speed** | Faster (no detection phase) | Slightly slower (detection overhead) |
+| **Accuracy** | Highest when library matches | Good, adapts to actual data |
+| **Robustness** | Fails if library doesn't match | Handles uncertainty |
+| **Use Case** | Known, standard protocols | Unknown or variable protocols |
+| **Error Handling** | Silent incorrect quantification | May detect unexpected patterns |
+
+## Current Usage in This Repository
+
+In `scripts/runMultiAlign.sh`, the repository uses:
+
+```bash
+--expected-ori fw
+```
+
+For single-cell RNA-seq with 10x Chromium:
+- `fw` (forward) is appropriate because the biological read (R2) is in the forward orientation
+- R1 contains the cell barcode + UMI (technical read)
+- R2 contains the actual cDNA sequence (biological read)
+
+This is functionally similar to specifying the strand orientation for the quantification step.
+
+## Recommendations
+
+### Use ISR (or fw for single-cell) when:
+1. Working with **standard 10x Chromium single-cell RNA-seq**
+2. Library prep protocol is **well-documented** and confirmed
+3. Processing **large production datasets** where speed matters
+4. Protocol has been **validated** on test samples
+
+### Use Auto mode when:
+1. **Protocol is uncertain** or from external sources
+2. **Testing new library prep methods**
+3. **Troubleshooting** quantification issues
+4. Working with **mixed samples** or unusual prep
+5. Want to **verify** the library orientation assumption
+
+## Checking Library Type
+
+After running salmon/alevin with auto mode, check the log file for:
+```
+Library format: ISR
+```
+
+This confirms what salmon detected and can inform future runs with explicit mode.
+
+## References
+
+- [Salmon Documentation - Library Type](https://salmon.readthedocs.io/en/latest/library_type.html)
+- [Alevin-fry Documentation](https://alevin-fry.readthedocs.io/)
+- [10x Genomics Library Structure](https://www.10xgenomics.com/)
+
+## Implementation in runMultiAlign.sh
+
+For the `runMultiAlign.sh` script:
+- Current implementation uses `--expected-ori fw` (explicit mode)
+- This is correct for standard 10x single-cell RNA-seq
+- To enable auto-detection, the syntax varies by tool
+
+**Important:** The specific syntax for auto-detection depends on the tool version. Always consult the documentation for your specific tool version before making changes.
+
+### Tool-Specific Auto Mode Syntax
+
+**For simpleaf (recommended for alevin-fry):**
+```bash
+# Current (explicit):
+--expected-ori fw --unfiltered-pl
+
+# Auto mode (simpleaf):
+--expected-ori both --unfiltered-pl
+```
+
+**For direct salmon-alevin usage:**
+```bash
+# Check your salmon version documentation
+# Older versions: may not support auto
+# Newer versions: typically support 'A' or 'both'
+```
+
+**For piscem:**
+```bash
+# Piscem typically follows salmon conventions
+# Consult piscem documentation for your version
+```
+
+### Verification Steps
+
+Before changing to auto mode in production:
+1. Test on a small subset of data first
+2. Check the output logs to confirm detected library type matches expectations
+3. Compare quantification results between explicit and auto modes
+4. Ensure detected type is consistently reported across samples