Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Quantify transcript expression using pseudo-alignment with Salmon or kallisto. Use when quantifying transcripts with Salmon or kallisto.
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See how to installReview the instructions the agent will receive before you install.
Reference examples tested with: Salmon 1.10+, fastp 0.23+, kallisto 0.50+, pandas 2.2+
Before using code patterns, verify installed versions match. If versions differ:
<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Quantify gene expression without alignment" → Estimate transcript abundances directly from FASTQ reads using pseudo-alignment or selective alignment, bypassing genome mapping.
salmon quant -i index -l A -1 R1.fq.gz -2 R2.fq.gz -o quant/, kallisto quant -i index -o output R1.fq.gz R2.fq.gzQuantify transcript abundance directly from FASTQ reads using pseudo-alignment (kallisto) or selective alignment (Salmon).
# Download transcriptome FASTA
# Ensembl: Homo_sapiens.GRCh38.cdna.all.fa.gz
# Basic index (fast, less accurate)
salmon index -t transcripts.fa -i salmon_index
# Decoy-aware index (recommended for accuracy)
# First, create decoys from genome
grep "^>" genome.fa | cut -d " " -f 1 | sed 's/>//g' > decoys.txt
cat transcripts.fa genome.fa > gentrome.fa
salmon index -t gentrome.fa -d decoys.txt -i salmon_index -p 8
# Paired-end reads
salmon quant -i salmon_index -l A \
-1 sample_R1.fastq.gz -2 sample_R2.fastq.gz \
-o sample_quant -p 8
# Single-end reads
salmon quant -i salmon_index -l A \
-r sample.fastq.gz \
-o sample_quant -p 8
Key flags:
-l A - Automatically detect library type-p - Number of threads--validateMappings - More accurate (default in recent versions)--gcBias - Correct for GC bias--seqBias - Correct for sequence-specific bias| Code | Description |
|---|---|
A | Automatic detection (recommended) |
ISR | Inward, stranded, read 1 from reverse |
ISF | Inward, stranded, read 1 from forward |
IU | Inward, unstranded |
for sample in sample1 sample2 sample3; do
salmon quant -i salmon_index -l A \
-1 ${sample}_R1.fastq.gz -2 ${sample}_R2.fastq.gz \
-o ${sample}_quant -p 8
done
sample_quant/
├── quant.sf # Main quantification file
├── aux_info/ # Auxiliary information
├── cmd_info.json # Command used
├── lib_format_counts.json # Library format detection
└── logs/ # Log files
quant.sf format:
Name Length EffectiveLength TPM NumReads
ENST00000456328.2 1657 1477.000 0.000000 0.000
ENST00000450305.2 632 452.000 12.345678 156.789
kallisto index -i kallisto_index transcripts.fa
# Paired-end
kallisto quant -i kallisto_index -o sample_quant \
sample_R1.fastq.gz sample_R2.fastq.gz
# Single-end (must specify fragment length)
kallisto quant -i kallisto_index -o sample_quant \
--single -l 200 -s 20 sample.fastq.gz
# With bootstraps (for sleuth)
kallisto quant -i kallisto_index -o sample_quant -b 100 \
sample_R1.fastq.gz sample_R2.fastq.gz
Key flags:
-b - Number of bootstrap samples-t - Number of threads--single - Single-end mode-l - Estimated fragment length (single-end)-s - Fragment length standard deviationsample_quant/
├── abundance.tsv # Main quantification (text)
├── abundance.h5 # HDF5 format (for sleuth)
└── run_info.json # Run information
abundance.tsv format:
target_id length eff_length est_counts tpm
ENST00000456328.2 1657 1477.00 0.00 0.000000
ENST00000450305.2 632 452.00 156.79 12.345678
| Feature | Salmon | kallisto |
|---|---|---|
| Speed | Fast | Fastest |
| Accuracy | Higher | Good |
| GC bias correction | Yes | No |
| Decoy sequences | Yes | No |
| Memory usage | Moderate | Low |
Recommendation: Use Salmon for production, kallisto for quick exploratory analysis.
# Salmon: use tximport in R
# kallisto: use tximport or sleuth
# Quick Python combination
python << 'EOF'
import pandas as pd
from pathlib import Path
samples = ['sample1', 'sample2', 'sample3']
tpm_data = {}
counts_data = {}
for sample in samples:
quant_file = Path(f'{sample}_quant/quant.sf') # Salmon
# quant_file = Path(f'{sample}_quant/abundance.tsv') # kallisto
df = pd.read_csv(quant_file, sep='\t', index_col=0)
tpm_data[sample] = df['TPM']
counts_data[sample] = df['NumReads'] # or est_counts for kallisto
tpm_matrix = pd.DataFrame(tpm_data)
counts_matrix = pd.DataFrame(counts_data)
tpm_matrix.to_csv('tpm_matrix.csv')
counts_matrix.to_csv('counts_matrix.csv')
EOF
# Check mapping rate from Salmon logs
grep "Mapping rate" sample_quant/logs/salmon_quant.log
# Check library type detection
cat sample_quant/lib_format_counts.json
Good metrics:
Low mapping rate:
Inconsistent library types:
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
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AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
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