polars-bio
Helps your agent perform operations on genomic intervals and read/write bioinformatics data formats. It's useful for genomic analyses and data joins.
What it does
This tool helps compare and manipulate genomic sequences (like genes in DNA). It allows you to find which sequences overlap, which are closest, merge continuous sequences, calculate coverage, and perform other operations.
When to use it
- ✓Comparing lists of genes to see which ones are common.
- ✓Finding DNA regions that were not covered by sequencing.
- ✓Merging overlapping pieces of genomic sequences.
Example of what to ask your AI
“Which genes in list A overlap with genes in list B?”
Want more? Open the sections below.
How to use
The easiest way: copy the message below and paste it into Claude, ChatGPT, Cursor or any AI. It reads the skill and follows the instructions.
Skill link
Ready-to-paste message
How it works
The tool reads genomic data in common formats (like BED, VCF, BAM) and organizes it into tables. It then applies mathematical operations to compare the positions of these genomic sequences.
Installation
Easiest way: copy the skill link and paste it into Claude, ChatGPT or Cursor asking it to follow the instructions.
In the terminal (Claude Code, Codex, Cursor), in your project folder:
npx skills add K-Dense-AI/scientific-agent-skills --skill polars-bioOr download just the file:
curl -L https://raw.githubusercontent.com/K-Dense-AI/scientific-agent-skills/main/skills/polars-bio/SKILL.md -o SKILL.mdTechnical content (original SKILL.md)
Original text by the author, straight from GitHub.
polars-bio
Use this skill for genomic interval arithmetic and bioinformatics file I/O through Polars and DataFusion. It targets polars-bio 0.36.0, tested with Polars 1.44.2 on Python 3.13. The upstream package requires Polars >=1.37.1, PyArrow >=23.0.1,<25, DataFusion >=53,<54 and polars-config-meta >=0.3.2,<1. Keep this environment separate from packages needing incompatible Arrow or DataFusion releases.
uv pip install "polars-bio==0.36.0" "polars==1.44.2"
# Optional pandas interoperability (requires pandas >=3):
uv pip install "polars-bio[pandas]==0.36.0" "polars==1.44.2"
Verify new releases against the official release notes and package requirements. The examples below with named files are templates: substitute actual files and check their schemas. The synthetic interval example and small local format round trips were executed during this review.
Workflow
- Record the assembly, contig naming, coordinate convention, strand policy and unit of analysis. Identical contig names do not prove identical assemblies.
- Choose readers by format; BCF has its own reader. Inspect schemas and source metadata before selecting attributes or genotypes.
- Normalize all inputs to one coordinate system and validate their bounds.
- Choose pair output, hit counts, covered bases or read depth deliberately.
- Filter and project lazily, then inspect a small result before scaling up.
- Validate output counts and boundaries against a hand-computable fixture; preserve IDs, coordinate metadata and provenance when saving results.
Coordinate contract
The default is 1-based closed, including converted BED reads. Use
use_zero_based=True on genomic readers for 0-based half-open output.
This argument converts positions; it is not only a metadata label. For example,
BED [0,10) becomes [1,10] by default and remains [0,10) with the override.
SAM text POS is 1-based, whereas BAM stores its alignment position internally
as 0-based. Both readers expose the requested output convention.
For manually constructed DataFrames, metadata labels existing numbers and
does not convert them. Converting closed [s,e] to half-open means s-1,e.
Set metadata only after conversion. Never convert twice.
import polars as pl
import polars_bio as pb
pb.set_option("datafusion.bio.coordinate_system_zero_based", True)
pb.set_option("datafusion.bio.coordinate_system_check", True)
query = pl.DataFrame({
"query_id": ["q1", "q2", "q3"],
"chrom": ["chr1", "chr1", "chr2"],
"start": [0, 10, 0], "end": [10, 20, 10],
})
target = pl.DataFrame({
"chrom": ["chr1", "chr1"], "start": [5, 8], "end": [12, 15],
})
for frame in (query, target):
frame.config_meta.set(coordinate_system_zero_based=True)
pairs = pb.overlap(query, target).collect()
counts = pb.count_overlaps(query, target).collect().sort("query_id")
covered = pb.coverage(query, target).collect().sort("query_id")
assert pairs.height == 4
assert counts["count"].to_list() == [2, 2, 0]
assert covered["coverage"].to_list() == [5, 5, 0]
Require non-null contigs, integer positions and valid positive-length intervals
(0 <= start < end in half-open form), within the chosen assembly. Do not silently
turn points/insertions into nonempty intervals: choose the biological convention.
Mismatched input metadata raises CoordinateSystemMismatchError; missing metadata
warns and uses the global setting by default, or raises MissingCoordinateSystemError
in strict mode. Inspect pb.get_metadata(frame) after transformations and SQL.
See configuration.
Choose the operation
| Question | Operation | Interpretation |
|---|---|---|
| Which interval pairs intersect? | overlap(a, b) |
Inner pair join; a query can appear repeatedly |
| Which query rows have any hit? | overlap(a, b, overlap_output="left", distinct_output=True) |
One hit per original query row; duplicate input rows retain identity |
| How many target intervals intersect each query? | count_overlaps(a, b) |
Target-record count, including zero for no hit |
| How many query bases are covered? | coverage(a, b) |
Length of the union of target intersections; not read depth |
| Which targets are closest? | nearest(a, b, k=1) |
Up to k neighbors, with nullable target/distance for no candidate |
…
FAQ
What are 'genomic intervals'?
They are stretches of DNA defined by a start and end point on a chromosome or larger sequence.
What file formats does it support?
It supports various formats used in molecular biology, such as BED, VCF, BAM, GFF, GTF, FASTA, and FASTQ.
How does it handle position counting (starting at 0 or 1)?
By default, it uses a 1-based (closed) counting system, but it can be configured to use a 0-based (half-open) system if needed, which is common in some tools.
Details
Original description by the author
Performs genomic interval overlap, nearest, merge, coverage, complement and subtraction on Polars DataFrames, and reads or writes BED, VCF, BCF, BAM, CRAM, GFF, GTF, FASTA and FASTQ data. Use for coordinate-aware genomic joins, read-depth analysis, lazy bioinformatics I/O, SQL queries or migration from bioframe.
Popularity
- GitHub stars
- 51k
- Ranking position
- #1937
- License
- MIT
- Updated
- 10/15/2026
Comments
- …
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