Testing associations of copy number variations in genome-wide association studies

MaRDI QIDQ2864538zbMATH OpenFDO

Authors Jianxin Shi, Peng Li

Publication date 25 November 2013

Published in Statistica Sinica (Search for Journal in Brave)

zbMATH Keywords

genome-wide association studycopy number variationTDTHidden Markov Modelfamily-based study

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10)

Recommendations

• Using GWAS data to identify copy number variants contributing to common complex diseases
• A likelihood-based framework for association analysis of allele-specific copy numbers
• Genotype copy number variations using Gaussian mixture models: theory and algorithms
• Association tests through combining \(p\)-values for case control genome-wide association studies
• The screening and ranking algorithm to detect DNA copy number variations

Cited in

(5)

• The biases of copy numbers from affymetrix SNP arrays and their corrections
• Testing neutrality at copy-number-variable loci under the finite-allele and finite-site models
• A likelihood-based framework for association analysis of allele-specific copy numbers
• Comparisons of BRAT1 gene variants
• Using GWAS data to identify copy number variants contributing to common complex diseases

This page was built for publication: Testing associations of copy number variations in genome-wide association studies

Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q2864538)