GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population
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Eleni Giannoulatou | Christopher Yau | Christopher C. Holmes | Jiannis Ragoussis | Stefano Colella | C. Yau | J. Ragoussis | S. Colella | C. Holmes | E. Giannoulatou
[1] Weihua Chang,et al. Whole-genome genotyping with the single-base extension assay , 2005, Nature Methods.
[2] M. Olivier. A haplotype map of the human genome , 2003, Nature.
[3] J. Q. Smith,et al. 1. Bayesian Statistics 4 , 1993 .
[4] Matthew J. Beal,et al. The variational Bayesian EM algorithm for incomplete data: with application to scoring graphical model structures , 2003 .
[5] D. Rubin,et al. Maximum likelihood from incomplete data via the EM - algorithm plus discussions on the paper , 1977 .
[6] David Harrington,et al. PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data. , 2007, Biostatistics.
[7] D. Conrad,et al. Global variation in copy number in the human genome , 2006, Nature.
[8] Terence P. Speed,et al. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias , 2003, Bioinform..
[9] Michael Inouye,et al. A genotype calling algorithm for the Illumina BeadArray platform , 2007, Bioinform..
[10] Joseph T. Glessner,et al. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. , 2007, Genome research.
[11] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[12] Geoffrey J. McLachlan,et al. Robust mixture modelling using the t distribution , 2000, Stat. Comput..
[13] P. Deloukas,et al. A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 , 2007, Nature Genetics.
[14] Michel Verleysen,et al. Robust Bayesian clustering , 2007, Neural Networks.