We report a method, Expression-Microarray Copy Number Analysis (ECNA) for the detection of copy number changes using Affymetrix Human Genome U133 Plus 2.0 arrays, starting with as little as 5 ng input genomic DNA. An analytical approach was developed using DNA isolated from cell lines containing various X-chromosome numbers, and validated with DNA from cell lines with defined deletions and amplifications in other chromosomal locations. We applied this method to examine the copy number changes in DNA from 5 frozen gastrointestinal stromal tumors (GIST). We detected known copy number aberrations consistent with previously published results using conventional or BAC-array CGH, as well as novel changes in GIST tumors. These changes were concord...
<div><p>Array-based comparative genomic hybridization (aCGH) is a powerful technique for detecting g...
textabstractBackground: Genes that play an important role in tumorigenesis are expected to show asso...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
AbstractTo identify DNA copy number changes that had a direct influence on mRNA expression in gastri...
Genomic instability with frequent DNA copy number alterations is one of the key hallmarks of carcino...
To identify DNA copy number changes that had a direct influence on mRNA expression in gastric cancer...
Background: Genomic instability with frequent DNA copy number alterations is one of the key hallmark...
Abstract Background To elucidate gene expression associated with copy number changes, we performed a...
Background: Genomic instability with frequent DNA copy number alterations is one of the key hallmark...
35 pagesInternational audienceIn this chapter, we focus on statistical questions raised by the ident...
Parallel analysis of gene expression and chromosomal copy number changes at high resolution in a gen...
In this work, we explore the use of representations in conjunction with DNA microarray technology to...
Abstract Background Genomic instability in cancer leads to abnormal genome copy number alterations (...
<div><p>The present study was aimed at discovering DNA copy number alterations (CNAs) involved in th...
In addition to KIT and PDGFRA mutations, sequential accumulation of other genetic events is involved...
<div><p>Array-based comparative genomic hybridization (aCGH) is a powerful technique for detecting g...
textabstractBackground: Genes that play an important role in tumorigenesis are expected to show asso...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
AbstractTo identify DNA copy number changes that had a direct influence on mRNA expression in gastri...
Genomic instability with frequent DNA copy number alterations is one of the key hallmarks of carcino...
To identify DNA copy number changes that had a direct influence on mRNA expression in gastric cancer...
Background: Genomic instability with frequent DNA copy number alterations is one of the key hallmark...
Abstract Background To elucidate gene expression associated with copy number changes, we performed a...
Background: Genomic instability with frequent DNA copy number alterations is one of the key hallmark...
35 pagesInternational audienceIn this chapter, we focus on statistical questions raised by the ident...
Parallel analysis of gene expression and chromosomal copy number changes at high resolution in a gen...
In this work, we explore the use of representations in conjunction with DNA microarray technology to...
Abstract Background Genomic instability in cancer leads to abnormal genome copy number alterations (...
<div><p>The present study was aimed at discovering DNA copy number alterations (CNAs) involved in th...
In addition to KIT and PDGFRA mutations, sequential accumulation of other genetic events is involved...
<div><p>Array-based comparative genomic hybridization (aCGH) is a powerful technique for detecting g...
textabstractBackground: Genes that play an important role in tumorigenesis are expected to show asso...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...