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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Библиографические подробности
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Cold Spring Harbor Laboratory Press 2004
Предметы:
Methods
Online-ссылка: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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