Related references
Note: Only part of the references are listed.PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
Kai Wang et al.
GENOME RESEARCH (2007)
A genotype calling algorithm for the Illumina BeadArray platform
Yik Y. Teo et al.
BIOINFORMATICS (2007)
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
David A. van Heel et al.
NATURE GENETICS (2007)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton et al.
NATURE (2007)
PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data
Thomas Laframboise et al.
BIOSTATISTICS (2007)
Robust Bayesian clustering
Cedric Archambeau et al.
NEURAL NETWORKS (2007)
Whole-genome genotyping with the single-base extension assay
FJ Steemers et al.
NATURE METHODS (2006)
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
BM Bolstad et al.
BIOINFORMATICS (2003)
Robust mixture modelling using the t distribution
D Peel et al.
STATISTICS AND COMPUTING (2000)
Share Paper
