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Article

VarB: a variation browsing and analysis tool for variants derived from next-generation sequencing data.

Bioinformatics (Oxford, England) - 15 Nov 2012

Preston Mark D, Manske Magnus, Horner Neil, Assefa Samuel, Campino Susana, Auburn Sarah, Zongo Issaka, Ouedraogo Jean-Bosco, Nosten Francois, Anderson Tim, Clark Taane G

Abstract excerpt

SUMMARY: There is an immediate need for tools to both analyse and visualize in real-time single-nucleotide polymorphisms, insertions and deletions, and other structural variants from new sequence file formats. We have developed VarB software that can be used to visualize variant call format files in real time, as well as identify regions under balancing selection and informative markers to differentiate...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22976080
DOI: 10.1093/bioinformatics/bts557
PMCID: PMC3496337

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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