Twelve years of SAMtools and BCFtools

Author:

Danecek Petr1ORCID,Bonfield James K1ORCID,Liddle Jennifer1ORCID,Marshall John2ORCID,Ohan Valeriu1ORCID,Pollard Martin O1ORCID,Whitwham Andrew1ORCID,Keane Thomas3ORCID,McCarthy Shane A1ORCID,Davies Robert M1ORCID,Li Heng45ORCID

Affiliation:

1. Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK

2. Wolfson Wohl Cancer Research Centre, Institute of Cancer Sciences, University of Glasgow, Switchback Road, Glasgow, G61 1QH, UK

3. EMBL-EBI, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SD, UK

4. Department of Data Sciences, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA

5. Department of Biomedical Informatics, Harvard Medical School, 10 Shattuck Street, Boston, MA 02215, USA

Abstract

Abstract Background SAMtools and BCFtools are widely used programs for processing and analysing high-throughput sequencing data. They include tools for file format conversion and manipulation, sorting, querying, statistics, variant calling, and effect analysis amongst other methods. Findings The first version appeared online 12 years ago and has been maintained and further developed ever since, with many new features and improvements added over the years. The SAMtools and BCFtools packages represent a unique collection of tools that have been used in numerous other software projects and countless genomic pipelines. Conclusion Both SAMtools and BCFtools are freely available on GitHub under the permissive MIT licence, free for both non-commercial and commercial use. Both packages have been installed >1 million times via Bioconda. The source code and documentation are available from https://www.htslib.org.

Funder

Wellcome Trust

Publisher

Oxford University Press (OUP)

Subject

Computer Science Applications,Health Informatics

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