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|created at=University of Virginia
|maintained=Yes
|input format=BED, BAM, GFF, VCF|output format=BED, BAM, GFF, VCF|sw feature=Feature overlaps, UNIX pipes, coverage, split-alignments, BAM support
|language=C++
|licence=GPLv2
|os=UNIX/Linux, Mac OS X,
}}
The BEDTools utilities allow one to address common genomics tasks such finding feature overlaps and computing coverage. In addition, one can develop sophisticated pipelines that answer complicated research questions by "streaming" several BEDTools together. The following are examples of common questions that one can address with BEDTools.
Calculating the depth and breadth of sequence coverage across defined "windows" in a genome.
The fact that all of the BEDTools accept input from “stdin” allows one to “stream / pipe” several commands together to facilitate more complicated analyses. Also, the tools allow fine control over how output is reported. Most recently, we have added support for sequence alignments in BAM (http://samtools.sourceforge.net/) format, as well as for features in GFF and “blocked” BED format. The tools are quite fast and typically finish in a matter of a few seconds, even for large datasets.
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