| name | sragent |
| description | Query the Sequence Read Archive (SRA), retrieve scientific publications, and analyze
genomics metadata using the SRAgent toolkit. Supports accession conversion (GSE→SRX→SRR),
BigQuery metadata queries, manuscript downloads from multiple sources, and scRNA-seq
technology identification. Use when working with SRA/GEO datasets, finding publications,
or analyzing single-cell sequencing experiments.
|
SRAgent: Sequence Read Archive Data and Publication Retrieval
Overview
SRAgent is an agentic workflow system for working with the NCBI Sequence Read Archive (SRA) and Gene Expression Omnibus (GEO) databases.
It automates literature discovery, metadata extraction, and manuscript retrieval for genomics datasets.
Setup Instructions
1. Install SRAgent
SRAgent requires Python ≥3.11. Check to see if SRAgent is already installed:
which SRAgent
If SRAgent is not installed, follow the instructions below.
Install using uv:
git clone https://github.com/ArcInstitute/SRAgent.git
cd SRAgent
uv venv
source .venv/bin/activate
uv pip install .
Verify installation:
SRAgent --help
2. Configure environment variables
The following environment variables are required:
OPENAI_API_KEY=sk-openai-...
- Needed to use OpenAI models
ANTHROPIC_API_KEY=sk-ant-...
- Needed to use Claude models
DYNACONF
- Needed to switch between Claude and OpenAI models
EMAIL=user@example.com
- Needed for using the Entrez API
NCBI_API_KEY=your-ncbi-key
- Optional for increased rate limits when using the Entrez API
CORE_API_KEY=your-core-key
- Optional for paper downloads from the CORE API
GCP_PROJECT_ID=your-project-id
- Needed for using Google BigQuery
GOOGLE_APPLICATION_CREDENTIALS=/path/to/key.json
- Needed for using Google BigQuery
Prompt the user to provide the environment variables if they are not already set as environment variables: export MY_SECRET_VAR=my-secret-value.
3. Configure Settings
SRAgent uses a settings file (settings.yml) to configure models and behavior.
The default configuration works for most users, but you can customize it.
Option A: Use Default Settings
No action needed - SRAgent ships with sensible defaults.
Option B: Custom Settings File
See ./references/example-settings.yml for an example settings file that you can modify as needed.
4. Verify Setup
Test your configuration:
python -c "from SRAgent.agents.utils import load_settings; s = load_settings(); print(s['models']['default'])"
SRAgent entrez "Convert GSE121737 to SRX accessions"
Core Capabilities
1. Accession Conversion
Convert between different genomics database accession formats:
- GEO Series: GSE* → SRA Study (SRP*)
- SRA Study: SRP*/PRJNA* → SRA Experiments (SRX*)
- SRA Experiment: SRX*/ERX* → SRA Runs (SRR*/ERR*)
2. Metadata Extraction
Query comprehensive metadata from SRA/GEO:
- Sequencing platform (Illumina, PacBio, Oxford Nanopore)
- Library preparation technology (10X Genomics, Smart-seq, etc.)
- Organism, tissue, cell type
- Study design and experimental details
- Single-cell vs bulk RNA-seq identification
3. BigQuery Analysis
Leverage NCBI's BigQuery dataset for large-scale queries:
- Batch accession conversions
- Technology identification across studies
- Filtering by platform, assay type, organism
- Study/experiment/run relationship mapping
4. Publication Retrieval
Automatically find and download manuscripts:
- Link SRA accessions to PubMed publications
- Extract DOIs from PubMed records
- Download full-text PDFs from multiple sources:
- Preprint servers (arXiv, bioRxiv, medRxiv)
- CORE API
- Europe PMC
- Unpaywall
- Batch processing with CSV input
When to Use This Skill
Use SRAgent when the user:
- Mentions SRA, GEO, or genomics accessions (GSE, SRP, SRX, SRR)
- Needs to convert between accession formats
- Wants metadata about sequencing experiments
- Needs to find or download papers associated with datasets
- References the Sequence Read Archive (SRA), European Nucleotide Archive (ENA), or Gene Expression Omnibus (GEO)
Available Commands
Command 1: SRAgent entrez
Purpose: Low-level NCBI Entrez database queries
Best for:
- Simple accession conversions
- Quick dataset summaries
- Cross-database linking
- When you know exactly what Entrez tool to use (esearch, efetch, elink)
Examples:
SRAgent --no-progress --no-summaries entrez "Convert GSE121737 to SRX accessions"
SRAgent --no-progress --no-summaries entrez "Summarize SRX4967527"
SRAgent --no-progress --no-summaries entrez "Find publications for GSE196830"
Command 2: SRAgent sragent
Purpose: Comprehensive metadata extraction with multiple tools
Best for:
- Complex metadata queries
- Technology identification
- When simple Entrez queries aren't enough
- Determining if data is single-cell
Tools available:
- Entrez agent (all databases)
- BigQuery (large-scale queries)
- NCBI web scraping
- sra-stat (direct sequence file analysis)
Examples:
SRAgent --no-progress --no-summaries sragent "Which 10X Genomics technology was used for ERX11887200?"
SRAgent --no-progress --no-summaries sragent "Summarize SRX4967527"
SRAgent --no-progress --no-summaries sragent "Is SRX4967527 single-cell RNA-seq data?"
SRAgent --no-progress --no-summaries sragent "What organism was sequenced in study PRJNA498286?"
Command 3: SRAgent papers
Purpose: Find and download manuscripts associated with SRA accessions
Best for:
- Downloading papers for datasets
- Batch retrieval of publications
- Enriching CSV files with DOIs and download paths
Input formats:
- Single accession:
SRX4967527
- Study accession:
SRP167700 or PRJNA498286
- CSV file with
accession column
Examples:
SRAgent --no-progress --no-summaries papers SRX4967527
SRAgent --no-progress --no-summaries papers PRJNA498286
SRAgent --no-progress --no-summaries papers accessions.csv --output-dir papers/
SRAgent --no-progress --no-summaries papers my-data.csv --accession-column "experiment_id"
SRAgent --no-progress --no-summaries papers accessions.csv --max-concurrency 3
Output:
- PDFs saved to
--output-dir/<accession>/
- Console summary showing:
- PubMed IDs found
- DOIs extracted
- Download success/failure status
- Updated CSV (when input is CSV) with columns:
pubmed_id
doi
download_path
Usage Patterns
Pattern 1: Dataset Investigation Workflow
SRAgent --no-progress --no-summaries entrez "Convert GSE121737 to SRX accessions"
SRAgent --no-progress --no-summaries sragent "For each SRX from GSE121737, determine: Is it single-cell? What library prep?"
SRAgent --no-progress --no-summaries papers GSE121737 --output-dir manuscripts/
Pattern 2: Technology Verification
SRAgent --no-progress --no-summaries sragent "Is SRX4967527 Illumina paired-end single-cell RNA-seq data?"
SRAgent --no-progress --no-summaries sragent "Which 10X Genomics chemistry was used: SRX4967527?"
SRAgent --no-progress --no-summaries sragent "What organism is SRX4967527?"
Pattern 3: Batch Processing
cat > accessions.csv << EOF
accession
SRX4967527
SRX4967528
SRX4967529
EOF
SRAgent --no-progress --no-summaries \
papers accessions.csv \
--output-dir papers/ \
--max-concurrency 5
Pattern 4: Study-Level Analysis
SRAgent --no-progress --no-summaries entrez "List all SRX accessions for study SRP167700"
SRAgent --no-progress --no-summaries entrez "Convert PRJNA498286 to SRX accessions"
SRAgent --no-progress --no-summaries sragent "Summarize the library prep technologies used in PRJNA498286"
Implementation Guide for Claude
Running SRAgent Commands
When the user needs SRAgent functionality, use the bash tool:
result = bash_tool(
command="SRAgent --no-progress --no-summaries entrez 'Convert GSE121737 to SRX accessions'",
description="Converting GEO accession to SRX format"
)
result = bash_tool(
command="SRAgent --no-progress --no-summaries sragent 'Which 10X technology was used for SRX4967527?'",
description="Determining library preparation technology"
)
result = bash_tool(
command="SRAgent --no-progress --no-summaries papers SRX4967527 --output-dir /home/claude/papers",
description="Downloading manuscripts for dataset"
)
Working with CSV Files
When processing batch data:
import pandas as pd
accessions = ["SRX4967527", "SRX4967528", "SRX4967529"]
df = pd.DataFrame({"accession": accessions})
df.to_csv("/home/claude/accessions.csv", index=False)
result = bash_tool(
command="SRAgent --no-progress --no-summaries papers /home/claude/accessions.csv --output-dir /home/claude/papers",
description="Batch downloading papers for multiple accessions"
)
enriched_df = pd.read_csv("/home/claude/accessions.csv")
Accession Format Reference
GEO (Gene Expression Omnibus)
- Series:
GSE + 5-7 digits (e.g., GSE121737)
- Sample:
GSM + 6-7 digits (e.g., GSM3457845)
SRA (Sequence Read Archive)
- Study:
SRP + 6 digits (e.g., SRP167700)
- Or BioProject:
PRJNA + 6 digits (e.g., PRJNA498286)
- Experiment:
SRX + 7-8 digits (e.g., SRX4967527)
- Run:
SRR + 7-8 digits (e.g., SRR8124405)
ENA (European Nucleotide Archive)
- Study:
ERP + 6 digits or PRJEB + 6 digits
- Experiment:
ERX + 7-8 digits (e.g., ERX11887200)
- Run:
ERR + 7-8 digits
Hierarchical Relationships
GEO Series (GSE)
↓
SRA Study (SRP) = BioProject (PRJNA)
↓
SRA Experiment (SRX) ← Links to → Publications (PubMed ID, DOI)
↓
SRA Run (SRR) [actual sequence files]
Common Single-Cell Technologies
SRAgent can identify these scRNA-seq technologies:
10X Genomics
- Chromium Single Cell 3' (v1, v2, v3)
- Chromium Single Cell 5'
- Chromium Single Cell ATAC
- Chromium Single Cell Multiome
- Visium Spatial
Other Platforms
- Smart-seq2 / Smart-seq3
- Drop-seq
- inDrop
- Seq-Well
- CEL-Seq2
- MARS-seq
- Quartz-Seq
Detection Strategy
SRAgent uses multiple signals:
- Library prep metadata fields
- Study descriptions and titles
- PubMed abstracts
- Sequence file characteristics (when using sra-stat)
Working Without BigQuery
If you don't have Google Cloud credentials:
SRAgent --no-progress --no-summaries entrez "Convert GSE121737 to SRX accessions"
SRAgent --no-progress --no-summaries papers SRX4967527
SRAgent --no-progress --no-summaries sragent "Which 10X technology for SRX4967527?"
Performance Optimization
SRAgent --no-progress --no-summaries papers large-dataset.csv \
--max-concurrency 10 \
--recursion-limit 150
SRAgent --no-progress --no-summaries papers accessions.csv \
--core-api-key "$CORE_API_KEY" \
--email "$EMAIL" \
--max-concurrency 5
Troubleshooting
"ModuleNotFoundError: No module named 'SRAgent'"
cd SRAgent
uv pip install .
python -c "import SRAgent; print(SRAgent.__file__)"
"Rate limit exceeded" (NCBI)
export NCBI_API_KEY="your-ncbi-api-key"
SRAgent papers accessions.csv --max-concurrency 3
Paper downloads fail
Resources
SRAgent Documentation
./references/metadata-fields.md
- All metadata fields that SRAgent can extract from SRA/GEO databases
./references/quick-reference.md
- Quick reference for SRAgent commands
./references/usage-examples.md
- Usage examples for SRAgent
./references/example-settings.yml
- Example settings file for SRAgent
External Resources