Alignment-Free Quantification

Quantify transcript abundance directly from FASTQ reads using pseudo-alignment (kallisto) or selective alignment (Salmon).

Salmon Workflow

Build Index

bash

# 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

Quantify Samples

bash

# 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

Library Types

Code	Description
`A`	Automatic detection (recommended)
`ISR`	Inward, stranded, read 1 from reverse
`ISF`	Inward, stranded, read 1 from forward
`IU`	Inward, unstranded

Batch Processing

bash

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

Output Files

code

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:

code

Name                    Length  EffectiveLength TPM         NumReads
ENST00000456328.2       1657    1477.000        0.000000    0.000
ENST00000450305.2       632     452.000         12.345678   156.789

kallisto Workflow

Build Index

bash

kallisto index -i kallisto_index transcripts.fa

Quantify Samples

bash

# 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 deviation

Output Files

code

sample_quant/
├── abundance.tsv      # Main quantification (text)
├── abundance.h5       # HDF5 format (for sleuth)
└── run_info.json      # Run information

abundance.tsv format:

code

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

Salmon vs kallisto

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.

Combining Results

bash

# 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

Quality Checks

bash

# 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:

•Mapping rate > 70%
•Consistent library type across samples

Common Issues

Low mapping rate:

•Wrong transcriptome version
•Contamination in samples
•Wrong library type

Inconsistent library types:

•Mixed library preparations
•Sample swap

Related Skills

•read-qc/fastp-workflow - Upstream preprocessing
•rna-quantification/tximport-workflow - Import results to R
•rna-quantification/count-matrix-qc - QC of quantification
•differential-expression/deseq2-basics - Downstream analysis