SNP Discovery in Pooled Samples With Mismatch Repair Detection

A targeted discovery effort is required to identify low frequency single nucleotide polymorphisms (SNPs) in human coding and regulatory regions. We here describe combining mismatch repair detection (MRD) with dideoxy terminator sequencing to detect SNPs in pooled DNA samples. MRD enriches for varian...

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Detalhes bibliográficos
Main Authors: Fakhrai-Rad, Hossein, Zheng, Jianbiao, Willis, Thomas D., Wong, Kee, Suyenaga, Kent, Moorhead, Martin, Eberle, Jim, Thorstenson, Yvonne R., Jones, Ted, Davis, Ronald W., Namsaraev, Eugeni, Faham, Malek
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2004
Assuntos:
Methods
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC442157/
https://ncbi.nlm.nih.gov/pubmed/15231755
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.2373904
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