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BEDTools: a flexible suite of utilities for comparing genomic features

Introduces BEDTools, an efficient C++ suite for comparing, manipulating, and annotating genomic features in BED, GFF, and BAM formats.

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BEDTools: a flexible suite of utilities for comparing genomic features

By A. Quinlan, Ira M. HallBioinform.
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The paper presents BEDTools, a flexible software suite for comparing, manipulating, and annotating genomic features stored in Browser Extensible Data (BED) and General Feature Format (GFF), addressing the fundamental genomics task of testing for overlaps and correlations between different sets of features. Beyond BED and GFF, the suite supports comparing sequence alignments in BAM format against these feature formats, and it is implemented in C++ for efficiency.

BEDTools is extremely efficient and lets users compare very large datasets, such as next-generation sequencing output, against both public and custom genome annotation tracks that were awkward to handle with existing web-based methods. Because its utilities can be combined with one another and with standard UNIX commands, BEDTools streamlines routine genomics work and supports pipelines that quickly answer intricate questions of large genomic datasets, with source code and a comprehensive manual freely available.

Abstract

Testing correlations between sets of genomic features is fundamental, but web-based overlap searches struggle with today's massive sequencing datasets. BEDTools is a suite for comparing, manipulating, and annotating genomic features in BED and GFF formats, and can compare BAM alignments against BED and GFF features. The tools are efficient, handle large sequencing datasets with public and custom annotation tracks, and chain with each other or standard UNIX commands to build pipelines. BEDTools is written in C++ with freely available source and documentation.

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bioinformaticsgenomic intervalssequence analysisBED/GFF/BAMnext-generation sequencing
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