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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...
Autores principales: | Ngamphiw, Chumpol, Kulawonganunchai, Supasak, Assawamakin, Anunchai, Jenwitheesuk, Ekachai, Tongsima, Sissades |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638149/ https://www.ncbi.nlm.nih.gov/pubmed/19091032 http://dx.doi.org/10.1186/1471-2105-9-S12-S9 |
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