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Query Genomic Databases

Get quick bioinformatics data like gene IDs, sequences, and annotations using the gget CLI or Python package. It runs BLAST-style searches and gathers evidence logs across genomic reference databases for your analysis.

affaan-m on GitHub

Curated by PromptsEdge from a public repo · MIT license. All credit goes to the author.

What is this skill?

Use this skill when a task needs quick bioinformatics lookup across genomic reference databases with the gget CLI or Python package.

When to use

  • Finding Ensembl IDs, gene metadata, transcript details, or sequences.
  • Running quick BLAST or BLAT lookups without building a full local pipeline.
  • Fetching reference genome links and annotations from Ensembl.
  • Querying protein structure, pathway, cancer, expression, or disease-association
  • Creating a reproducible first-pass evidence log before moving to heavier

Installation

Use a clean Python environment.

bash
python -m venv .venv
. .venv/bin/activate
python -m pip install --upgrade pip
python -m pip install --upgrade gget
gget --help

If uv is available:

bash
uv venv
. .venv/bin/activate
uv pip install gget

Before relying on an older environment, upgrade gget and re-check the module docs. The upstream databases queried by gget change over time.

Basic Patterns

CLI shape:

bash
gget <module> [arguments] [options]

Python shape:

python
import gget

result = gget.search(["BRCA1"], species="human")
print(result)

Common workflow:

  1. Identify the species, assembly, gene ID type, and database needed.
  2. Check the current module documentation for arguments.
  3. Run a small query first.
  4. Save output with an explicit filename and date.
  5. Record module name, version, arguments, and database assumptions.

Common Modules

Use current upstream docs for exact arguments. These modules are common first choices:

  • gget search: find Ensembl IDs from search terms.
  • gget info: retrieve metadata for Ensembl, UniProt, or related IDs.
  • gget seq: fetch nucleotide or amino-acid sequences.
  • gget ref: retrieve reference genome download links.
  • gget blast: run a quick BLAST query.
  • gget blat: locate a sequence against supported genome assemblies.
  • gget muscle: run multiple sequence alignment.
  • gget diamond: run local sequence alignment against reference sequences.
  • gget alphafold and gget pdb: inspect protein-structure references.
  • gget enrichr, gget opentargets, gget archs4, gget bgee, gget cbio, and gget cosmic: explore enrichment, target, expression, cancer, and disease association data.

Do not assume every module supports every Python version or dependency set. Some optional scientific dependencies have narrower version support than the core package.

Quick Examples

Find genes:

bash
gget search -s human brca1 dna repair -o brca1-search.json

Fetch gene metadata:

bash
gget info ENSG00000012048 -o brca1-info.json

Fetch a sequence:

bash
gget seq ENSG00000012048 -o brca1-seq.fa

Run a small BLAST query:

bash
gget blast "MEEPQSDPSVEPPLSQETFSDLWKLLPEN" -l 10 -o blast-results.json

Python example:

python
import gget

genes = gget.search(["BRCA1", "DNA repair"], species="human")
info = gget.info(["ENSG00000012048"])
sequence = gget.seq("ENSG00000012048")

Reproducibility Log

For scientific outputs, include enough metadata to replay the query.

markdown
| Date | gget version | Module | Query | Species/assembly | Output | Notes |
| --- | --- | --- | --- | --- | --- | --- |
| 2026-05-11 | `gget --version` | search | `BRCA1 DNA repair` | human | `brca1-search.json` | Docs checked before run |

Also record:

  • Python version and environment manager.
  • Any optional dependency installed through gget setup.
  • Database-specific identifiers returned by the query.
  • Whether output is JSON, CSV, FASTA, or a DataFrame export.
  • Any failures that were resolved by upgrading gget.

Review Checklist

  • Did you upgrade or verify the installed gget version?
  • Did you check the current upstream module docs before using arguments?
  • Is the species or assembly explicit?
  • Are identifiers preserved exactly, including Ensembl/UniProt prefixes?
  • Is the result labeled as database output rather than clinical interpretation?
  • Is the query reproducible from the saved command or Python snippet?
  • Are optional dependencies installed in an isolated environment?

References

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