KRLMM: an adaptive genotype calling method for common and low frequency variants

BACKGROUND: SNP genotyping microarrays have revolutionized the study of complex disease. The current range of commercially available genotyping products contain extensive catalogues of low frequency and rare variants. Existing SNP calling algorithms have difficulty dealing with these low frequency v...

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Detalles Bibliográficos
Autores principales: Liu, Ruijie, Dai, Zhiyin, Yeager, Meredith, Irizarry, Rafael A, Ritchie, Matthew E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064501/
https://www.ncbi.nlm.nih.gov/pubmed/24886250
http://dx.doi.org/10.1186/1471-2105-15-158

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064501/
https://www.ncbi.nlm.nih.gov/pubmed/24886250
http://dx.doi.org/10.1186/1471-2105-15-158

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