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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Bibliografische gegevens
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Cold Spring Harbor Laboratory Press 2004
Onderwerpen:
Methods
Online toegang: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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