Assessing batch effects of genotype calling algorithm BRLMM for the Affymetrix GeneChip Human Mapping 500 K array set using 270 HapMap samples

BACKGROUND: Genome-wide association studies (GWAS) aim to identify genetic variants (usually single nucleotide polymorphisms [SNPs]) across the entire human genome that are associated with phenotypic traits such as disease status and drug response. Highly accurate and reproducible genotype calling a...

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Detalles Bibliográficos
Autores principales: Hong, Huixiao, Su, Zhenqiang, Ge, Weigong, Shi, Leming, Perkins, Roger, Fang, Hong, Xu, Joshua, Chen, James J, Han, Tao, Kaput, Jim, Fuscoe, James C, Tong, Weida
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2537568/
https://www.ncbi.nlm.nih.gov/pubmed/18793462
http://dx.doi.org/10.1186/1471-2105-9-S9-S17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2537568/
https://www.ncbi.nlm.nih.gov/pubmed/18793462
http://dx.doi.org/10.1186/1471-2105-9-S9-S17

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