Guide · Agent skill
How to use the Gtars Genomic Interval Toolkit agent skill
Updated · written with AI from the project's own documentation and checked against our catalogue data
The gtars skill gives an AI agent a careful workflow for genomic interval files, which are BED-style regions, using the Gtars library in Python, Rust, or its command-line tool. This guide explains what the skill changes about the agent's behaviour, how to install it from the downloaded ZIP, how to ask for work in plain language, and what safety conditions apply. By the end you will know how to set it up and what to review before letting it run analysis.
Quick start
- 1Download and unzip. Download the gtars skill ZIP from the skill page and unzip it into ~/.claude/skills/ or a project's .claude/skills/ folder.
- 2Or upload in the Claude apps. If you use the Claude apps, open Settings → Capabilities → Skills and upload the ZIP instead.
- 3Check Python and review the package. Confirm you have Python 3.10 or newer, and review the Gtars package source, license and checksums before installing.
- 4Create an isolated environment. Use uv or pip to install Gtars into a separate environment so it does not affect your other projects.
- 5Validate your interval file. Ask the agent to validate the BED file against your assembly and chromosome sizes, or run the bundled validator yourself.
- 6Run the analysis with limits. Ask for the overlap, coverage or set operation you need, and set limits and an output folder before the run starts.
- 7Review the results. Check the row counts, sort order and provenance notes the agent reports before using any output.
What the gtars skill makes the agent do
Without a skill, an agent will often write quick scripts that load a BED file and count overlaps without checking the data. The gtars skill changes that. Before analysis, the agent is told to check coordinates, assembly, chromosome names and strand, and to run bundled local validators that inspect files without changing them.
The skill covers set operations, overlaps and counts, consensus and coverage, tokenization, fragment processing, and refget/BEDbase planning. It is written for Python, Rust and the gtars command-line tool, and asks for explicit approval before any network access or downloads.
- Validate BED interval files against an assembly and chromosome sizes before use
- Compare and combine interval sets with overlaps, intersections, reduction and coverage
- Plan refget and BEDbase work, which requires approval for network and storage
Install the gtars skill from the ZIP
Download the skill ZIP from the skill page and unzip it. For a personal setup, place the folder in ~/.claude/skills/. For a single project, place it in the project's .claude/skills/ folder so that only that project uses it.
In the Claude apps, you can instead upload the ZIP under Settings → Capabilities → Skills. Either way, the skill's own files are the ones described in SKILL.md, including its scripts and reference notes.
- Personal: ~/.claude/skills/
- Project only: .claude/skills/ inside the project folder
- Claude apps: Settings → Capabilities → Skills, then upload the ZIP
Check the requirements and safety notes first
The skill needs Python 3.10 or newer. The Python package is a native extension from PyPI, and the skill's examples were exercised on Python 3.12. Rust and gtars-cli are optional, for command-line or Rust use, and need a Rust toolchain that supports Edition 2024. uv or pip can set up an isolated environment.
Treat installation as running code. Installing Gtars through Python loads native code, and installing the CLI through Cargo compiles native code and may run dependency build scripts. The skill asks you to confirm the official source, review the release and checksums, and use isolation and resource limits. Remote constructors, pretrained tokenizers, refget and BEDbase caching all need explicit network and storage approval. The bundled audit scripts use only the Python standard library and make no network calls.
- Python 3.10 or newer; optional Rust toolchain for CLI or Rust work
- Installing the package runs native code: review it first
- Network access, downloads and caching need your explicit approval
- Scripts run locally; the bundled inspectors do not change input files
Ask for work in plain language
You do not need special command syntax. Describe the file and the goal, for example that you have a BED file and want to check it against a named assembly, or that you want to know how two region sets overlap or how much of one is covered by the other. The skill's description lists the tasks it supports, so requests that match those tasks are the ones it is built for.
Give the agent the details it needs to follow the data contract: the assembly, the chromosome sizes file if you have one, whether the file must be sorted, and where outputs should go. If you do not know the assembly, say so; the skill is designed not to guess it from filenames or chr prefixes.
- Validate: "Check this BED file against GRCh38 before I use it"
- Compare: "Count how many query regions overlap the universe file"
- Summarise: "Give me the fraction of these peaks covered by the gene set"
Run the local validator on a BED file
The skill's first step is a local validator that inspects a file without changing it. You can run the same command yourself to see what the agent will check. It asks for an assembly label, a chromosome sizes file and a sorting requirement.
The validator enforces the coordinate rules: BED intervals are 0-based and half-open, start must be less than end, and no end may exceed its contig length. Contig names must match exactly, so 1 and chr1 are treated as different names.
python3 -B scripts/bed_validator.py --input data.bed.gz --assembly GRCh38.p14 --chrom-sizes GRCh38.p14.chrom.sizes --require-sortedUse the Python API for overlaps and coverage
In Python, gtars models are imported from submodules rather than the top-level gtars package. RegionSet holds a set of intervals, and methods such as count_overlaps, any_overlaps and coverage return one result per query region or a single fraction, depending on the method.
Set RegionSet.sort() mutates the object and returns None, so do not assign its result. File-backed RegionSet objects sort lexicographically by contig and start when loaded, so do not rely on original row order. Loading does not merge overlapping intervals; call reduce() when you want that.
- Import from gtars.models, for example Region and RegionSet
- Overlap methods use ordinary half-open overlap, so [0,10) and [10,20) do not overlap
- reduce(), and consensus, merge overlapping and adjacent intervals
from gtars.models import Region, RegionSet
query = RegionSet.from_regions([Region(chr="chr1", start=100, end=200, rest=None)], strands=["+"])
universe = RegionSet.from_vectors(["chr1"], [150], [350])
counts = query.count_overlaps(universe)
fraction = query.coverage(universe)Keep strand and provenance under your control
The skill warns that strand is not reliably carried through every operation. A file-backed RegionSet starts its strand list as unspecified, sort() does not reorder that list, and several set operations drop strand. If strand matters scientifically, validate it separately and keep the original file.
The skill also asks for provenance: record file checksums, the assembly accession, the lockfile and artifact hashes, and the resource limits used. Outputs should go to a dedicated folder, and existing files should not be overwritten unless you approve it.
- Keep the original file and sort a copy when an operation needs sorting
- Record checksums, assembly, and library versions with the results
- Set limits on input size, memory, disk and run time for larger jobs
What people use it for
- Checking a set of called peaks against a named assembly before comparing them with a gene annotation
- Counting how many variant or region records overlap a reference universe, with ordinary half-open overlap rules
- Computing the fraction of a region set covered by another set for a coverage summary
- Merging adjacent and overlapping regions with reduce() before building a consensus interval set
- Planning a refget or BEDbase workflow, with network and storage approval recorded first
Frequently asked questions
Is the gtars skill free to use?
The skill itself is listed under the MIT license. The Gtars packages declare MIT, but the source notes that the GitHub repository currently shows BSD-2-Clause at its root, so check the exact artifact's license before you redistribute it.
What do I need to install the gtars skill?
You need Python 3.10 or newer for the Python package. The Rust toolchain and gtars-cli are optional, for command-line or Rust use, and the skill's examples were tested on Python 3.12.
Where do I put the skill folder after downloading it?
Unzip it into ~/.claude/skills/ for personal use, or into a project's .claude/skills/ folder for one project. In the Claude apps you can upload the ZIP under Settings → Capabilities → Skills.
Does the skill access the internet?
The skill uses the network for some features, such as remote constructors, pretrained tokenizers, refget and BEDbase caching. Each of these needs your explicit approval, and the bundled audit scripts run locally without network calls.
Why does the validator say my chromosome names do not match?
Chromosome names are compared exactly, so 1, chr1, alternate loci, decoys and mitochondrial aliases are not treated as the same. Rename contigs only as a separate, reviewed step, and never infer the assembly from a chr prefix.
Can I use this for clinical or patient-facing decisions?
No. The skill is a technical tool and its outputs need expert validation, so it is not meant for clinical or patient-facing decisions.
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Our verdict
Use the gtars skill if you are a bioinformatician or developer who needs to validate and compare BED interval files with repeatable steps, and you are willing to review the native code before installing it. Pick another approach if you want one-click analysis without reading installed code, or if your workflow depends on remote data fetching that you cannot approve.
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