pybedtools documentation — pybedtools 0.10.0 documentation (original) (raw)

Overview¶

The BEDTools suite of programs 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, athttp://daler.github.io/pybedtools/.

Why `pybedtools`?¶

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

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 thepybedtools version above:

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−bsnps -b snps−bgenes -v > $intergenic_snps

closestBed -a genes−bgenes -b genes−bintergenic_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 in the docs for more details on this comparison, or keep reading the full documentation athttp://daler.github.io/pybedtools.

As of 2022, pybedtools is released under the MIT license; see LICENSE.txt for more info.

Note

If you use pybedtools in your work, please cite the pybedtools manuscriptand the BEDTools manuscript:

Dale RK, Pedersen BS, and Quinlan AR. 2011. Pybedtools: a flexible Python library for manipulating genomic datasets and annotations. Bioinformatics 27(24):3423-3424.

Quinlan AR and Hall IM, 2010. BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 26(6):841–842.

Getting started¶

The documentation is separated into 4 main parts, depending on the depth you’d like to cover:

Lazy, or just want to jump in? Check out Three brief examples to get a feel for the package.
Want a guided tour? Give the Tutorial Contents a shot.
More advanced features are described in the Topical Documentation section.
Finally, doctested module documentation can be found in pybedtools Reference.

pybedtools documentation — pybedtools 0.10.0 documentation (original) (raw)

Overview¶

Why `pybedtools`?¶

Getting started¶

Contents:¶

Indices and tables¶

pybedtools documentation — pybedtools 0.10.0 documentation (original) (raw)

Overview¶

Why pybedtools?¶

Getting started¶

Contents:¶

Indices and tables¶

Why `pybedtools`?¶