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Article

BAM-matcher: a tool for rapid NGS sample matching.

Bioinformatics (Oxford, England) - 1 Sept 2016

Wang Paul P S, Parker Wendy T, Branford Susan, Schreiber Andreas W

Abstract excerpt

UNLABELLED: The standard method used by high-throughput genome sequencing facilities for detecting mislabelled samples is to use independently generated high-density SNP data to determine sample identity. However, as it has now become commonplace to have multiple samples sequenced from the same source, such as for analysis of somatic variants using matched tumour and normal samples, we can directly use the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27153667
DOI: 10.1093/bioinformatics/btw239

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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