SNP and gene networks construction and analysis from classification of copy number variations data

Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays

(2010) Derek A. Oldridge et al.   NUCLEIC ACIDS RESEARCH

A Bayesian segmentation approach to ascertain copy number variations at the population level

(2009) Long Yang Wu et al.   BIOINFORMATICS

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

(2009) J. O. Korbel et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Sparse representation and Bayesian detection of genome copy number alterations from microarray data

(2008) Roger Pique-Regi et al.   BIOINFORMATICS

Comparison of the Agilent, ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors

(2008) LO Baumbusch et al.   BMC GENOMICS

Classification of human cancers based on DNA copy number amplification modeling

(2008) Samuel Myllykangas et al.   BMC Medical Genomics

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS