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A Novel Support Vector Machine-Based Approach for Rare Variant Detection

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 fe...

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Detalhes bibliográficos
Main Authors: Fang, Yao-Hwei, Chiu, Yen-Feng
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3737136/
https://ncbi.nlm.nih.gov/pubmed/23940698
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0071114
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