Identification of disease causing loci using an array-based genotyping approach on pooled DNA

BACKGROUND: Pooling genomic DNA samples within clinical classes of disease followed by genotyping on whole-genome SNP microarrays, allows for rapid and inexpensive genome-wide association studies. Key to the success of these studies is the accuracy of the allelic frequency calculations, the ability...

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Detalles Bibliográficos
Autores principales: Craig, David W, Huentelman, Matthew J, Hu-Lince, Diane, Zismann, Victoria L, Kruer, Michael C, Lee, Anne M, Puffenberger, Erik G, Pearson, John M, Stephan, Dietrich A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1262713/
https://www.ncbi.nlm.nih.gov/pubmed/16197552
http://dx.doi.org/10.1186/1471-2164-6-138

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1262713/
https://www.ncbi.nlm.nih.gov/pubmed/16197552
http://dx.doi.org/10.1186/1471-2164-6-138

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