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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Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Cold Spring Harbor Laboratory Press 2004
Konular:
Methods
Online Erişim: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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