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Article

A probabilistic method for the detection and genotyping of small indels from population-scale sequence data.

Bioinformatics (Oxford, England) - 1 Aug 2011

Bansal Vikas, Libiger Ondrej

Abstract excerpt

MOTIVATION: High-throughput sequencing technologies have made population-scale studies of human genetic variation possible. Accurate and comprehensive detection of DNA sequence variants is crucial for the success of these studies. Small insertions and deletions represent the second most frequent class of variation in the human genome after single nucleotide polymorphisms (SNPs). Although several alignment tools...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 21653520
DOI: 10.1093/bioinformatics/btr344
PMCID: PMC3137221

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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