Genotyping platforms such as Affymetrix can be used to assess genotype-phenotype as well as copy number-phenotype associations at millions of markers. While genotyping algorithms are largely concordant when assessed on HapMap samples, tools to assess copy number changes are more variable and often discordant. One explanation for the discordance is that copy number estimates are susceptible to systematic differences between groups of samples that were processed at different times or by different labs. Analysis algorithms that do not adjust for batch effects are prone to spurious measures of association. The R package crlmm implements a multilevel model that adjusts for batch effects and provides allele-specific estimates of copy number. This...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Motivation: The discovery that copy number variants (CNVs) are widespread in the human genome has mo...
The discovery that copy number variants (CNVs) are widespread in the human genome has motivated deve...
Genotyping platforms such as Affymetrix can be used to assess genotype-phenotype as well as copy num...
Submicroscopic changes in chromosomal DNA copy number dosage are common and have been implicated in ...
Submicroscopic changes in chromosomal DNA copy number dosage are common and have been implicated in ...
Abstract Background Copy number data are routinely be...
The fast development of high-throughput technologies enabled us to access to more than 1.5 million m...
Over recent years small submicroscopic DNA copy-number variants (CNVs) have been highlighted as an i...
Recently, structural variation in the genome has been implicated in many complex diseases. Using gen...
The analysis of structural variants, in particular of copy-number variations (CNVs), has proven valu...
Received on; revised on; accepted on Motivation: DNA copy number variants (CNV) are gains and losses...
National audienceMPAgenomics, standing for multi-patients analysis of genomicmarkers, is an R-packag...
Background: Genomic deletions and duplications are important in the pathogenesis of...
Abstract Background Genome-wide association studies (GWAS) aim to identify genetic variants (usually...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Motivation: The discovery that copy number variants (CNVs) are widespread in the human genome has mo...
The discovery that copy number variants (CNVs) are widespread in the human genome has motivated deve...
Genotyping platforms such as Affymetrix can be used to assess genotype-phenotype as well as copy num...
Submicroscopic changes in chromosomal DNA copy number dosage are common and have been implicated in ...
Submicroscopic changes in chromosomal DNA copy number dosage are common and have been implicated in ...
Abstract Background Copy number data are routinely be...
The fast development of high-throughput technologies enabled us to access to more than 1.5 million m...
Over recent years small submicroscopic DNA copy-number variants (CNVs) have been highlighted as an i...
Recently, structural variation in the genome has been implicated in many complex diseases. Using gen...
The analysis of structural variants, in particular of copy-number variations (CNVs), has proven valu...
Received on; revised on; accepted on Motivation: DNA copy number variants (CNV) are gains and losses...
National audienceMPAgenomics, standing for multi-patients analysis of genomicmarkers, is an R-packag...
Background: Genomic deletions and duplications are important in the pathogenesis of...
Abstract Background Genome-wide association studies (GWAS) aim to identify genetic variants (usually...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Motivation: The discovery that copy number variants (CNVs) are widespread in the human genome has mo...
The discovery that copy number variants (CNVs) are widespread in the human genome has motivated deve...