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Article

A novel support vector machine-based approach for rare variant detection.

PloS one - 1 Jan 2013

Fang Yao-Hwei, Chiu Yen-Feng

Abstract excerpt

Advances in next-generation sequencing technologies have enabled the identification of multiple rare single nucleotide polymorphisms involved in diseases or traits. Several strategies for identifying rare variants that contribute to disease susceptibility have recently been proposed. An important...

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Identifiers

PMID: 23940698
DOI: 10.1371/journal.pone.0071114
PMCID: PMC3737136

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23940698-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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