Submicroscopic changes in chromosomal DNA copy number dosage are common and have been implicated in many heritable diseases and cancers. Recent high-throughput technologies have a resolution that permits the detection of segmental changes in DNA copy number that span thousands of basepairs across the genome. Genome-wide association studies (GWAS) may simultaneously screen for copy number-phenotype and SNP-phenotype associations as part of the analytic strategy. However, genome-wide array analyses are particularly susceptible to batch effects as the logistics of preparing DNA and processing thousands of arrays often involves multiple laboratories and technicians, or changes over calendar time to the reagents and laboratory equipment. Failure...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
35 pagesInternational audienceIn this chapter, we focus on statistical questions raised by the ident...
Recently, structural variation in the genome has been implicated in many complex diseases. Using gen...
Submicroscopic changes in chromosomal DNA copy number dosage are common and have been implicated in ...
Genotyping platforms such as Affymetrix can be used to assess genotype-phenotype as well as copy num...
We propose a statistical framework, named genoCN, to simultaneously dissect copy number states and g...
Genotyping platforms such as Affymetrix can be used to assess genotype-phenotype as well as copy num...
This study describes a new tool for accurate and reliable high-throughput detection of copy number v...
Background: Genomic deletions and duplications are important in the pathogenesis of...
The detection of copy number variants (CNV) by array-based platforms provides valuable insight into ...
Abstract Background SNP arrays, short- and long-read genome sequencing are genome-wide high-throughp...
Affymetrix single-nucleotide polymorphism (SNP) arrays have been widely used for SNP genotype callin...
Determination of copy number variants (CNVs) inferred in genome wide single nucleotide polymorphism ...
Copy number variation (CNV) is pervasive in the human genome and has been shown to contribute signif...
Recent advances in genomics have underscored the surprising ubiquity of DNA copy number variants (CN...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
35 pagesInternational audienceIn this chapter, we focus on statistical questions raised by the ident...
Recently, structural variation in the genome has been implicated in many complex diseases. Using gen...
Submicroscopic changes in chromosomal DNA copy number dosage are common and have been implicated in ...
Genotyping platforms such as Affymetrix can be used to assess genotype-phenotype as well as copy num...
We propose a statistical framework, named genoCN, to simultaneously dissect copy number states and g...
Genotyping platforms such as Affymetrix can be used to assess genotype-phenotype as well as copy num...
This study describes a new tool for accurate and reliable high-throughput detection of copy number v...
Background: Genomic deletions and duplications are important in the pathogenesis of...
The detection of copy number variants (CNV) by array-based platforms provides valuable insight into ...
Abstract Background SNP arrays, short- and long-read genome sequencing are genome-wide high-throughp...
Affymetrix single-nucleotide polymorphism (SNP) arrays have been widely used for SNP genotype callin...
Determination of copy number variants (CNVs) inferred in genome wide single nucleotide polymorphism ...
Copy number variation (CNV) is pervasive in the human genome and has been shown to contribute signif...
Recent advances in genomics have underscored the surprising ubiquity of DNA copy number variants (CN...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
35 pagesInternational audienceIn this chapter, we focus on statistical questions raised by the ident...
Recently, structural variation in the genome has been implicated in many complex diseases. Using gen...