Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays

Identification of the genetic basis of common disease may require comprehensive sequence analysis of coding regions and regulatory elements in patients and controls to find genetic effects caused by rare or heterogeneous mutations. In this study, we demonstrate how mismatch repair detection on tag a...

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Bibliografiske detaljer
Main Authors: Faham, Malek, Zheng, Jianbiao, Moorhead, Martin, Fakhrai-Rad, Hossein, Namsaraev, Eugeni, Wong, Kee, Wang, Zhiyong, Chow, Shu G., Lee, Liana, Suyenaga, Kent, Reichert, Jennifer, Boudreau, Andrew, Eberle, James, Bruckner, Carsten, Jain, Maneesh, Karlin-Neumann, George, Jones, Hywel B., Willis, Thomas D., Buxbaum, Joseph D., Davis, Ronald W.
Format: Artigo
Sprog:Inglês
Udgivet: National Academy of Sciences 2005
Fag:
Biological Sciences
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1253580/
https://ncbi.nlm.nih.gov/pubmed/16203980
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0506677102
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