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Pybedtools

Python wrapper -- and more -- for BEDTools (bioinformatics tools for "genome arithmetic")

Install / Use

/learn @daler/Pybedtools
About this skill

Quality Score

0/100

Supported Platforms

Universal

README

Overview

.. image:: https://badge.fury.io/py/pybedtools.svg?style=flat :target: https://badge.fury.io/py/pybedtools

.. image:: https://img.shields.io/badge/install%20with-bioconda-brightgreen.svg :target: https://bioconda.github.io

The BEDTools suite of programs <http://bedtools.readthedocs.org/>_ is widely used for genomic interval manipulation or "genome algebra". pybedtools wraps and extends BEDTools and offers feature-level manipulations from within Python.

See full online documentation, including installation instructions, at https://daler.github.io/pybedtools/.

The GitHub repo is at https://github.com/daler/pybedtools.

Why pybedtools?

Here is an example to get the names of genes that are <5 kb away from intergenic SNPs:

.. code-block:: python

from pybedtools import BedTool

snps = BedTool('snps.bed.gz')  # [1]
genes = BedTool('hg19.gff')    # [1]

intergenic_snps = snps.subtract(genes)                       # [2]
nearby = genes.closest(intergenic_snps, d=True, stream=True) # [2, 3]

for gene in nearby:             # [4]
    if int(gene[-1]) < 5000:    # [4]
        print gene.name         # [4]

Useful features shown here include:

  • [1] support for all BEDTools-supported formats (here gzipped BED and GFF)
  • [2] wrapping of all BEDTools programs and arguments (here, subtract and closest and passing the -d flag to closest);
  • [3] streaming results (like Unix pipes, here specified by stream=True)
  • [4] iterating over results while accessing feature data by index or by attribute access (here [-1] and .name).

In contrast, here is the same analysis using shell scripting. Note that this requires knowledge in Perl, bash, and awk. The run time is identical to the pybedtools version above:

.. code-block:: bash

snps=snps.bed.gz
genes=hg19.gff
intergenic_snps=/tmp/intergenic_snps

snp_fields=`zcat $snps | awk '(NR == 2){print NF; exit;}'`
gene_fields=9
distance_field=$(($gene_fields + $snp_fields + 1))

intersectBed -a $snps -b $genes -v > $intergenic_snps

closestBed -a $genes -b $intergenic_snps -d \
| awk '($'$distance_field' < 5000){print $9;}' \
| perl -ne 'm/[ID|Name|gene_id]=(.*?);/; print "$1\n"'

rm $intergenic_snps

See the Shell script comparison <http://daler.github.io/pybedtools/sh-comparison.html>_ in the docs for more details on this comparison, or keep reading the full documentation at http://daler.github.io/pybedtools.

View on GitHub
GitHub Stars329
CategoryDevelopment
Updated13d ago
Forks106

Languages

Python

Security Score

80/100

Audited on Mar 14, 2026

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