PlatinumCNV: A Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data
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Title
PlatinumCNV: A Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data
Authors
Keywords
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Journal
GENETIC EPIDEMIOLOGY
Volume 35, Issue 8, Pages 831-844
Publisher
Wiley
Online
2011-11-29
DOI
10.1002/gepi.20633
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Note: Only part of the references are listed.- Mapping copy number variation by population-scale genome sequencing
- (2011) Ryan E. Mills et al. NATURE
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- (2010) Lachlan J M Coin et al. NATURE METHODS
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- (2009) Jon Wakefield BIOMETRICS
- CYP2D6 Genotyping for Functional-Gene Dosage Analysis by Allele Copy Number Detection
- (2009) N. Hosono et al. CLINICAL CHEMISTRY
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
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- (2009) Donald F. Conrad et al. NATURE
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
- (2009) Sekar Kathiresan et al. NATURE GENETICS
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
- (2009) L. A. Hindorff et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Detection, Imputation, and Association Analysis of Small Deletions and Null Alleles on Oligonucleotide Arrays
- (2008) Lude Franke et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Sparse representation and Bayesian detection of genome copy number alterations from microarray data
- (2008) Roger Pique-Regi et al. BIOINFORMATICS
- Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
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- (2008) Steven A McCarroll et al. NATURE GENETICS
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
- (2008) Joshua M Korn et al. NATURE GENETICS
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