affaan-m/ECC

gget

gget CLI and Python workflow for quick genomic database queries, sequence lookup, BLAST-style searches, enrichment checks, and reproducible bioinformatics evidence logs.

94CollectingRuns scripts
See how to use itView GitHub source
npx skills add https://github.com/affaan-m/ECC --skill "skills/scientific-pkg-gget"

Quick start

Start using it in three steps

Install it or open the source, trigger it with a clear task, then follow the source workflow.

1

Install the Skill

npx skills add https://github.com/affaan-m/ECC --skill "skills/scientific-pkg-gget"
2

Describe the task

Use gget to help me with: [describe your task]. Before you begin, tell me what input you need, the steps you will follow, and the expected output.

3

Follow the workflow

No structured workflow was detected; follow the original SKILL.md below.

Continue to the workflow

Direct answers

Answers to review before you install

What is gget?

gget CLI and Python workflow for quick genomic database queries, sequence lookup, BLAST-style searches, enrichment checks, and reproducible bioinformatics evidence logs.

Who should use gget?

It is relevant to workflows involving Operations, Python.

How do you install gget?

SkillSignal detected this source-specific command: npx skills add https://github.com/affaan-m/ECC --skill "skills/scientific-pkg-gget". Inspect the repository and command before running it.

Which Agent platforms does it support?

The upstream source does not declare a dedicated Agent platform.

What permissions or risks should you review?

Static analysis detected exec-script signals. Review the cited source lines before installing; these signals are not a security audit.

What are the current evidence limits?

This page combines upstream documentation with deterministic repository, quality, and static-risk signals. It is not described as a manual test or security review.

SkillSignal brief

Decide whether it fits your work first

gget CLI and Python workflow for quick genomic database queries, sequence lookup, BLAST-style searches, enrichment checks, and reproducible bioinformatics evidence logs.

Useful in these contexts

Not yet included in a workflow collection

Core capabilities

OperationsPython

Distilled from the source

Understand this Skill in one minute

About 3 min · 9 sections

When it is worth using

  1. Finding Ensembl IDs, gene metadata, transcript details, or sequences.

  2. Running quick BLAST or BLAT lookups without building a full local pipeline.

  3. Fetching reference genome links and annotations from Ensembl.

  4. Querying protein structure, pathway, cancer, expression, or disease-association

Repository stars
234,327
Repository forks
35,711
Quality
94/100
Source repository last pushed

Quality breakdown

Based on traceable docs and repository signals; stars are not treated as quality.

94/100
Documentation28/30
Specificity23/25
Maintenance20/20
Trust signals23/25

Compare before choosing

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These links are selected from shared tasks, functions, stacks, platforms, and same-name variants. Compare the source owner, documentation, permissions, and maintenance signals.

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View original Skill.mdThis page is parsed directly from the repository SKILL.md without editorial rewriting. Collected: Jul 28, 2026 · about 3 min

gget

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 modules through a single interface.
  • Creating a reproducible first-pass evidence log before moving to heavier tools such as Biopython, Snakemake, Nextflow, BLAST+, or database-specific clients.

Use a dedicated workflow instead of gget when the task requires regulated clinical interpretation, high-throughput production pipelines, or fine-grained control over database versions and local indexes.

Installation

Use a clean Python environment.

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:

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:

gget <module> [arguments] [options]

Python shape:

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:

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

Fetch gene metadata:

gget info ENSG00000012048 -o brca1-info.json

Fetch a sequence:

gget seq ENSG00000012048 -o brca1-seq.fa

Run a small BLAST query:

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

Python example:

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.

| 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

Source repo
affaan-m/ECC
Skill path
skills/scientific-pkg-gget/SKILL.md
Commit SHA
4e973d3eaf92
Repository license
MIT
Data collected