The study of somatic genetic alterations in tumors contributes to the understanding and management of cancer. Genetic alterations, such us copy number or copy neutral changes, generate allelic imbalances (AIs) that can be determined using polymorphic markers. Here we report the development of a simple set of calculations for analyzing microsatellite multiplex PCR data from control-tumor pairs that allows us to obtain accurate information not only regarding the AI status of tumors, but also the percentage of tumor-infiltrating normal cells, the locus copy-number status and the mechanism involved in AI. We validated this new approach by re-analyzing a set of Neurofibromatosis type 1-associated dermal neurofibromas and comparing newly generate...
Detection of microsatellite instability (MSI) is the standard part of mutational analysis in heredit...
*<p>see text for details.</p><p>Analysis of the copy number status of the <i>NF1</i> locus in 29 neu...
The extent to which heritable genetic variants can affect tumor development has yet to be fully eluc...
The study of somatic genetic alterations in tumors contributes to the understanding and management o...
The study of somatic genetic alterations in tumors contributes to the understanding and management o...
Background: Single nucleotide polymorphisms (SNPs) are the most common genetic variations in the hum...
Abstract Background The Multiplex Ligation-dependent Probe Amplification (MLPA) is widely used for a...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
Identifying microsatellite instability (MSI) by partitioning DNA into multiple small pools containin...
Abstract Background Genomic instability in cancer leads to abnormal genome copy number alterations (...
Genomic copy number changes are detectable in many malignancies, including neuroblastoma, using tech...
Objectives. The chief goal of this study was to analyze copy number variation (CNV) in breast cancer...
International audienceBackground: High-throughput genotyping microarrays assess both total DNA copy ...
35 pagesInternational audienceIn this chapter, we focus on statistical questions raised by the ident...
In the pediatric cancer neuroblastoma, analysis of recurrent chromosomal aberrations such as loss of...
Detection of microsatellite instability (MSI) is the standard part of mutational analysis in heredit...
*<p>see text for details.</p><p>Analysis of the copy number status of the <i>NF1</i> locus in 29 neu...
The extent to which heritable genetic variants can affect tumor development has yet to be fully eluc...
The study of somatic genetic alterations in tumors contributes to the understanding and management o...
The study of somatic genetic alterations in tumors contributes to the understanding and management o...
Background: Single nucleotide polymorphisms (SNPs) are the most common genetic variations in the hum...
Abstract Background The Multiplex Ligation-dependent Probe Amplification (MLPA) is widely used for a...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
Identifying microsatellite instability (MSI) by partitioning DNA into multiple small pools containin...
Abstract Background Genomic instability in cancer leads to abnormal genome copy number alterations (...
Genomic copy number changes are detectable in many malignancies, including neuroblastoma, using tech...
Objectives. The chief goal of this study was to analyze copy number variation (CNV) in breast cancer...
International audienceBackground: High-throughput genotyping microarrays assess both total DNA copy ...
35 pagesInternational audienceIn this chapter, we focus on statistical questions raised by the ident...
In the pediatric cancer neuroblastoma, analysis of recurrent chromosomal aberrations such as loss of...
Detection of microsatellite instability (MSI) is the standard part of mutational analysis in heredit...
*<p>see text for details.</p><p>Analysis of the copy number status of the <i>NF1</i> locus in 29 neu...
The extent to which heritable genetic variants can affect tumor development has yet to be fully eluc...