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GPTomics

bio-sra-data

by GPTomics

a set of SKILLS.md for doing bioinformatics with agents like claude code

65🍴 17📅 Jan 24, 2026

SKILL.md


name: bio-sra-data description: Download sequencing data from NCBI SRA using the SRA toolkit. Use when downloading FASTQ files from SRA accessions, prefetching large datasets, or validating SRA downloads. tool_type: cli primary_tool: sra-tools

SRA Data

Download raw sequencing data from the Sequence Read Archive using the SRA toolkit.

Installation

# macOS
brew install sratoolkit

# Ubuntu/Debian
sudo apt install sra-toolkit

# conda (recommended)
conda install -c bioconda sra-tools

# Verify installation
fasterq-dump --version

Core Commands

Fast, multithreaded FASTQ extraction. Preferred over fastq-dump.

# Download single SRA run as FASTQ
fasterq-dump SRR12345678

# Output: SRR12345678.fastq (single-end)
# Or: SRR12345678_1.fastq, SRR12345678_2.fastq (paired-end)

Key Options:

OptionDescriptionExample
-O / --outdirOutput directory-O ./fastq/
-o / --outfileOutput filename-o sample.fastq
-e / --threadsNumber of threads-e 8
-p / --progressShow progress bar-p
-S / --split-filesSplit paired reads (default)-S
-3 / --split-3Also output unpaired reads-3
--skip-technicalSkip technical reads--skip-technical
-t / --tempTemp directory-t /tmp
-f / --forceOverwrite existing-f
# Common usage with options
fasterq-dump SRR12345678 -O ./data/ -e 8 -p --skip-technical

# Force split files (paired-end)
fasterq-dump SRR12345678 -S -O ./data/

prefetch - Download SRA Files First

For large files or unreliable connections, prefetch first, then convert.

# Prefetch SRA file (downloads .sra to ~/ncbi/sra/)
prefetch SRR12345678

# Then convert to FASTQ
fasterq-dump ~/ncbi/sra/SRR12345678.sra

# Or convert in place
fasterq-dump SRR12345678  # Will find prefetched file

Prefetch Options:

OptionDescription
-O / --output-directoryDownload location
-p / --progressShow progress
-f / --forceRe-download if exists
--max-sizeMax file size (e.g., 50G)
-X / --max-sizeSame as above
# Prefetch with size limit
prefetch SRR12345678 --max-size 100G -p

# Prefetch multiple accessions
prefetch SRR12345678 SRR12345679 SRR12345680

# Prefetch from a list file
prefetch --option-file accessions.txt

vdb-validate - Verify Downloads

Check integrity of downloaded SRA files.

# Validate a downloaded file
vdb-validate SRR12345678

# Validate with detailed output
vdb-validate SRR12345678 2>&1

sra-stat - Get Run Statistics

Get information about an SRA run without downloading.

# Basic stats
sra-stat --quick SRR12345678

# Detailed XML output
sra-stat --xml SRR12345678

Configuration

vdb-config - Configure SRA Toolkit

Set up cache location and other settings.

# Interactive configuration
vdb-config -i

# Set cache directory
vdb-config --set /repository/user/main/public/root=/path/to/cache

# Check current configuration
vdb-config --cfg

Cache Location

Default: ~/ncbi/ on Linux/macOS

# Create dedicated cache
mkdir -p /data/sra_cache
vdb-config --set /repository/user/main/public/root=/data/sra_cache

Code Patterns

Download Single Run

#!/bin/bash
SRR="SRR12345678"
OUTDIR="./fastq"

mkdir -p $OUTDIR
fasterq-dump $SRR -O $OUTDIR -e 8 -p

Download Multiple Runs

#!/bin/bash
# From a list of accessions
while read SRR; do
    echo "Downloading $SRR..."
    fasterq-dump $SRR -O ./fastq/ -e 4 -p
done < accessions.txt

Prefetch Then Convert (Large Files)

#!/bin/bash
SRR="SRR12345678"

# Prefetch first (resumable)
prefetch $SRR -p

# Validate
vdb-validate $SRR

# Convert to FASTQ
fasterq-dump $SRR -O ./fastq/ -e 8 -p

# Optionally remove .sra file
rm -f ~/ncbi/sra/${SRR}.sra

Batch Download Script

#!/bin/bash
# download_sra.sh - Download multiple SRA runs

ACCESSIONS="$1"
OUTDIR="${2:-./fastq}"
THREADS="${3:-4}"

mkdir -p $OUTDIR

while read SRR; do
    if [[ -z "$SRR" ]] || [[ "$SRR" == \#* ]]; then
        continue
    fi

    echo "Processing $SRR..."

    # Prefetch
    prefetch $SRR -p -O $OUTDIR

    # Validate
    if ! vdb-validate ${OUTDIR}/${SRR}/${SRR}.sra 2>/dev/null; then
        echo "Validation failed for $SRR, skipping..."
        continue
    fi

    # Convert
    fasterq-dump ${OUTDIR}/${SRR}/${SRR}.sra -O $OUTDIR -e $THREADS -p

    # Cleanup .sra
    rm -rf ${OUTDIR}/${SRR}

    echo "Completed $SRR"
done < "$ACCESSIONS"

Python Wrapper

import subprocess
import os

def download_sra(accession, outdir='.', threads=4, skip_technical=True):
    os.makedirs(outdir, exist_ok=True)

    cmd = ['fasterq-dump', accession, '-O', outdir, '-e', str(threads), '-p']
    if skip_technical:
        cmd.append('--skip-technical')

    result = subprocess.run(cmd, capture_output=True, text=True)
    if result.returncode != 0:
        raise RuntimeError(f"fasterq-dump failed: {result.stderr}")

    return result.stdout

# Download a run
download_sra('SRR12345678', outdir='./data', threads=8)

Find SRA Accessions with Entrez

from Bio import Entrez

Entrez.email = 'your.email@example.com'

def find_sra_runs(term, max_results=100):
    handle = Entrez.esearch(db='sra', term=term, retmax=max_results)
    search = Entrez.read(handle)
    handle.close()

    if not search['IdList']:
        return []

    handle = Entrez.efetch(db='sra', id=','.join(search['IdList']), rettype='runinfo', retmode='text')
    runinfo = handle.read()
    handle.close()

    # Parse CSV-like output
    runs = []
    for line in runinfo.strip().split('\n')[1:]:
        if line:
            fields = line.split(',')
            if len(fields) > 0:
                runs.append(fields[0])  # First field is Run accession
    return runs

# Find runs for a project
runs = find_sra_runs('PRJNA123456[bioproject]')
print(f"Found {len(runs)} runs")

SRA Accession Types

PrefixTypeDescription
SRRRunIndividual sequencing run
SRXExperimentExperimental design
SRSSampleBiological sample
SRPProject/StudyResearch project
PRJNABioProjectNCBI BioProject ID
SAMNBioSampleNCBI BioSample ID

Use Run accessions (SRR*) with fasterq-dump.

Common Errors

ErrorCauseSolution
item not foundInvalid accessionCheck accession exists
disk fullInsufficient spaceCheck temp and output dirs
timeoutNetwork issuesUse prefetch first
path not foundBad output pathCreate output directory
permission deniedCache permissionCheck vdb-config

Comparison: fasterq-dump vs fastq-dump

Featurefasterq-dumpfastq-dump
SpeedFast (multithreaded)Slow (single-threaded)
MemoryHigherLower
ProgressBuilt-inNone
RecommendedYesLegacy only

Always prefer fasterq-dump unless memory constrained.

Decision Tree

Need SRA sequencing data?
├── Know the SRR accession?
│   └── fasterq-dump SRR... -O ./fastq/ -p
├── Large file (>20GB)?
│   └── prefetch first, then fasterq-dump
├── Multiple runs?
│   └── Loop through accessions or use prefetch --option-file
├── Need to find accessions?
│   └── Search SRA database with Entrez
├── Download interrupted?
│   └── prefetch supports resume
└── Verify integrity?
    └── vdb-validate SRR...
  • entrez-search - Search SRA database to find accessions
  • sequence-io - Read downloaded FASTQ files with Biopython
  • sequence-io/paired-end-fastq - Handle paired R1/R2 files
  • alignment-files - Align downloaded reads

Score

Total Score

65/100

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