pybedtools
pybedtools copied to clipboard
Python wrapper -- and more -- for BEDTools (bioinformatics tools for "genome arithmetic")
Overview
.. image:: https://travis-ci.org/daler/pybedtools.png?branch=master :target: https://travis-ci.org/daler/pybedtools
.. image:: https://badge.fury.io/py/pybedtools.svg?style=flat :target: http://badge.fury.io/py/pybedtools
.. image:: https://img.shields.io/badge/install%20with-bioconda-brightgreen.svg :target: http://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 http://daler.github.io/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
andclosest
and passing the-d
flag toclosest
); -
[3]
streaming results (like Unix pipes, here specified bystream=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.