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...
Background\ud Genomic instability in cancer leads to abnormal genome copy number alterations (CNA) a...
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...
The study of somatic genetic alterations in tumors contributes to the understanding and management o...
<div><p>The study of somatic genetic alterations in tumors contributes to the understanding and mana...
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...
BACKGROUND:Single nucleotide polymorphisms (SNPs) are the most common genetic variations in the huma...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
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 (...
Abstract Background Single nucleotide polymorphisms (SNPs) are the most common genetic variations in...
Background\ud Genomic instability in cancer leads to abnormal genome copy number alterations (CNA) a...
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...
The study of somatic genetic alterations in tumors contributes to the understanding and management o...
<div><p>The study of somatic genetic alterations in tumors contributes to the understanding and mana...
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...
BACKGROUND:Single nucleotide polymorphisms (SNPs) are the most common genetic variations in the huma...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
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 (...
Abstract Background Single nucleotide polymorphisms (SNPs) are the most common genetic variations in...
Background\ud Genomic instability in cancer leads to abnormal genome copy number alterations (CNA) a...
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...