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VarDetect: a nucleotide sequence variation exploratory tool

BACKGROUND: Single nucleotide polymorphisms (SNPs) are the most commonly studied units of genetic variation. The discovery of such variation may help to identify causative gene mutations in monogenic diseases and SNPs associated with predisposing genes in complex diseases. Accurate detection of SNPs...

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Detalhes bibliográficos
Main Authors: Ngamphiw, Chumpol, Kulawonganunchai, Supasak, Assawamakin, Anunchai, Jenwitheesuk, Ekachai, Tongsima, Sissades
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2638149/
https://ncbi.nlm.nih.gov/pubmed/19091032
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-9-S12-S9
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