BamToCov: an efficient toolkit for sequence coverage calculations.

Bioinformatics

Gut Microbes and Health Programme, Quadram Institute Bioscience, Norwich Research Park, Norwich NR4 7UQ, UK.

Published: April 2022

Motivation: Many genomics applications require the computation of nucleotide coverage of a reference genome or the ability to determine how many reads map to a reference region.

Results: BamToCov is a toolkit for rapid and flexible coverage computation that relies on the most memory efficient algorithm and is designed for integration in pipelines, given its ability to read alignment files from streams. The tools in the suite can process sorted BAM or CRAM files, allowing the user to extract coverage information via different filtering approaches and to save the output in different formats (BED, Wig or counts). The BamToCov algorithm can also handle strand-specific and/or physical coverage analyses.

Availability And Implementation: This program, accessory utilities and their documentation are freely available at https://github.com/telatin/BamToCov.

Supplementary Information: Supplementary data are available at Bioinformatics online.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048650PMC
http://dx.doi.org/10.1093/bioinformatics/btac125DOI Listing

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