geo-database
The geo-database skill provides programmatic access to NCBI's Gene Expression Omnibus (GEO) repository, enabling users to search for publicly available genomic datasets by keyword, organism, or platform, download GEO series (GSE) with expression matrices and metadata, and parse sample annotations into pandas DataFrames. Use this skill when retrieving microarray or bulk RNA-seq expression data, extracting sample metadata for meta-analysis, or building automated pipelines that integrate GEO datasets into downstream analysis workflows.
git clone --depth 1 https://github.com/jaechang-hits/SciAgent-Skills /tmp/geo-database && cp -r /tmp/geo-database/skills/genomics-bioinformatics/databases/geo-database ~/.claude/skills/geo-databaseSKILL.md
# GEO Gene Expression Omnibus Database
## Overview
GEO (Gene Expression Omnibus) is NCBI's public repository for high-throughput functional genomics data, containing 200,000+ datasets (series) from microarrays, RNA-seq, ChIP-seq, methylation, and proteomics experiments. GEOparse provides a Python interface for downloading and parsing GEO records (GSE series, GPL platforms, GSM samples) while NCBI E-utilities enables programmatic search across GEO's metadata.
## When to Use
- Searching for publicly available gene expression datasets by organism, tissue, disease, or experimental condition
- Downloading and parsing a specific GEO series (GSE) with its expression matrix and sample metadata
- Extracting sample annotation tables (e.g., treatment groups, clinical covariates) for meta-analysis
- Loading microarray expression data (GPL platform-annotated probes) into a tidy DataFrame
- Retrieving all GEO experiments associated with a gene or pathway of interest
- Building automated pipelines that download and process GEO datasets for downstream analysis
- For single-cell RNA-seq data at scale, use `cellxgene-census`; for aligned reads, download FASTQ from ENA/SRA instead
## Prerequisites
- **Python packages**: `GEOparse`, `requests`, `pandas`
- **Data requirements**: GSE/GPL/GSM accession numbers, or search terms
- **Environment**: internet connection; write access to local directory for downloads
- **Rate limits**: E-utilities: 3 req/s unauthenticated, 10 req/s with API key; GEO FTP is unlimited
```bash
pip install GEOparse requests pandas
```
## Quick Start
```python
import GEOparse
# Download a GEO series (caches in current directory)
gse = GEOparse.get_GEO("GSE2553", destdir="./geo_data/")
print(f"Title: {gse.metadata['title'][0]}")
print(f"Samples: {len(gse.gsms)}")
print(f"Platform: {list(gse.gpls.keys())}")
# Sample metadata
meta = gse.phenotype_data
print(meta.head())
```
## Core API
### Query 1: Search GEO Datasets via E-utilities
Find GEO series (GSE) by keyword, organism, or dataset type.
```python
import requests
EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"
def geo_search(query, retmax=20):
r = requests.get(f"{BASE}/esearch.fcgi",
params={"db": "gds", "term": query,
"retmax": retmax, "retmode": "json", "email": EMAIL})
r.raise_for_status()
return r.json()["esearchresult"]
# Search for human breast cancer RNA-seq datasets
result = geo_search(
"breast cancer[title] AND Homo sapiens[organism] AND gse[entry type]",
retmax=10
)
print(f"Found {result['count']} matching GEO datasets")
print(f"First accessions (UIDs): {result['idlist']}")
```
```python
# Search for specific platform (e.g., Illumina HumanHT-12)
result = geo_search(
"Illumina HumanHT-12[platform] AND Homo sapiens[organism] AND gse[entry type]",
retmax=5
)
print(f"Illumina HumanHT-12 human datasets: {result['count']}")
```
### Query 2: Fetch Dataset Summary Metadata
Retrieve title, accession, and organism for search results.
```python
import requests
EMAIL = "your@email.com"
BASE = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils"
def geo_summary(uids):
r = requests.post(f"{BASE}/esummary.fcgi",
data={"db": "gds", "id": ",".join(uids),
"retmode": "json", "email": EMAIL})
r.raise_for_status()
return r.json()["result"]
# Get metadata for search results
result = geo_search_func = lambda q: requests.get(
f"{BASE}/esearch.fcgi",
params={"db": "gds", "term": q, "retmax": 3, "retmode": "json", "email": EMAIL}
).json()["esearchresult"]["idlist"]
uids = requests.get(
f"{BASE}/esearch.fcgi",
params={"db": "gds", "term": "lung cancer[title] AND gse[entry type]",
"retmax": 3, "retmode": "json", "email": EMAIL}
).json()["esearchresult"]["idlist"]
summaries = geo_summary(uids)
for uid in summaries.get("uids", []):
s = summaries[uid]
print(f"\nAccession: {s.get('accession')} | {s.get('title')}")
print(f" Organism: {s.get('taxon')}")
print(f" Samples: {s.get('n_samples')}")
print(f" Type: {s.get('gdstype')}")
```
### Query 3: Download and Parse a GEO Series
Use GEOparse to download a full GSE record with expression matrix and sample metadata.
```python
import GEOparse
# Download GSE (auto-caches; skip download if already present)
gse = GEOparse.get_GEO("GSE2553", destdir="./geo_data/", silent=True)
# Series metadata
print(f"Title : {gse.metadata['title'][0]}")
print(f"Summary : {gse.metadata['summary'][0][:200]}...")
print(f"Samples : {len(gse.gsms)} GSMs")
print(f"Platforms: {list(gse.gpls.keys())}")
```
```python
# Sample metadata table (phenotype data)
meta = gse.phenotype_data
print(f"Metadata columns: {list(meta.columns)}")
print(meta.head())
```
### Query 4: Extract Expression Matrix
Parse probe-level expression data and optionally merge with platform gene annotations.
```python
import GEOparse, pandas as pd
gse = GEOparse.get_GEO("GSE2553", destdir="./geo_data/", silent=True)
# Pivot to gene expression matrix (probes × samples)
gpl_id = list(gse.gpls.keys())[0]
pivot = gse.pivot_samples("VALUE", gpl_id)
print(f"Expression matrix shape: {pivot.shape}") # (probes, samples)
print(pivot.iloc[:5, :3])
```
```python
# Annotate probes with gene symbols from the GPL platform
gpl = gse.gpls[gpl_id]
annot = gpl.table[["ID", "Gene Symbol", "Gene Title"]].copy()
annot.columns = ["ID", "gene_symbol", "gene_title"]
annot = annot.dropna(subset=["gene_symbol"])
annot = annot[annot["gene_symbol"] != ""]
expr_annotated = pivot.join(annot.set_index("ID"), how="inner")
print(f"Annotated expression matrix: {expr_annotated.shape}")
print(expr_annotated[["gene_symbol", "gene_title"]].head())
```
### Query 5: Download Individual Sample (GSM)
Retrieve expression values and metadata for a single sample.
```python
import GEOparse
gsm = GEOparse.get_GEO("GSM45553", destdir="./geo_data/", silent=TruAnnotated matrices for single-cell genomics. Stores X with obs/var metadata, layers, embeddings (obsm/varm), graphs (obsp/varp), uns. Use for .h5ad/.zarr I/O, concatenation, scverse integration. For analysis use scanpy; for probabilistic models use scvi-tools.
GRN inference from expression via GRNBoost2 (gradient boosting) or GENIE3 (Random Forest). Load matrix, filter by TFs, infer TF-target-importance links, save network. Dask-parallelized to single-cell scale. Core SCENIC component.
Query ARCHS4 REST API for uniformly processed RNA-seq expression, tissue patterns, co-expression across 1M+ human/mouse samples. Retrieve z-scores, co-expressed genes, samples by metadata, HDF5 matrices. For variant population genetics use gnomad-database; for pathway enrichment use gget-genomic-databases (Enrichr).
Annotate bacterial and archaeal genomes and plasmids with Bakta's Prodigal/HMM/diamond pipeline. Identifies CDS, ncRNA, tRNA, rRNA, tmRNA, sORFs, CRISPR arrays, oriC/oriV/oriT, and gaps against a curated UniRef-derived database. Produces NCBI-compatible GFF3, GenBank, EMBL, JSON, FASTA, TSV, and a circular genome plot. Use Prokka for legacy pipelines or non-bacterial kingdoms; PGAP for NCBI GenBank submission.
CLI for VCF/BCF: filter, merge, annotate, query, normalize, compute stats. Core post-variant-calling: quality filtering, multi-sample merging, rsID annotation, genotype extraction. Samtools companion in HTSlib. Use GATK for complex indel realignment during calling; use VCFtools for population genetics stats.
Genomic interval ops on BED/BAM/GFF/VCF. Find overlaps, merge intervals, compute coverage, extract FASTA, find nearest features. Core for ChIP-seq peak annotation, region filtering, genome arithmetic. Use tabix for indexed single-region queries; use deeptools for normalized bigWig coverage.
Molecular biology toolkit: sequence manipulation, FASTA/GenBank/PDB I/O, NCBI Entrez, BLAST automation, pairwise/MSA alignment, Bio.PDB, phylogenetic trees. Use for batch processing, custom pipelines, format conversion, PubMed/GenBank queries. For quick gene lookups use gget; for multi-service REST APIs use bioservices.
Biopython sequence analysis: parse FASTA/FASTQ/GenBank/GFF (SeqIO), NCBI Entrez (esearch/efetch/elink), remote/local BLAST, pairwise/MSA alignment (PairwiseAligner, MUSCLE/ClustalW), phylogenetic trees (Phylo). Use for gene family studies, phylogenomics, comparative genomics, NCBI pipelines. For PCR/restriction/cloning use biopython-molecular-biology; for SAM/BAM use pysam.