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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Detalles Bibliográficos
Autores principales: Ngamphiw, Chumpol, Kulawonganunchai, Supasak, Assawamakin, Anunchai, Jenwitheesuk, Ekachai, Tongsima, Sissades
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research
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

Internet

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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