We describe a bioinformatic tool, Tumor Aberration Prediction Suite (TAPS), for the identification of allele-specific copy numbers in tumor samples using data from Affymetrix SNP arrays. It includes detailed visualization of genomic segment characteristics and iterative pattern recognition for copy number identification, and does not require patient-matched normal samples. TAPS can be used to identify chromosomal aberrations with high sensitivity even when the proportion of tumor cells is as low as 30%. Analysis of cancer samples indicates that TAPS is well suited to investigate samples with aneuploidy and tumor heterogeneity, which is commonly found in many types of solid tumors
Accurate identification of copy number alterations is an essential step in understanding the events ...
<div><p>Background</p><p>Tumor single nucleotide polymorphism (SNP) array is a common platform for i...
Array-based genotyping platforms have during recent years been established as a valuable tool for th...
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...
BACKGROUND: Using whole exome sequencing to predict aberrations in tumours is a cost effective alter...
The application of genome-wide approaches to the molecular characterization of cancer was investigat...
International audienceIn clinical cancer research, high throughput genomic technologies are increasi...
Abstract Background Genomic aberrations can be used to determine cancer diagnosis and prognosis. Cli...
AbstractIn clinical cancer research, high throughput genomic technologies are increasingly used to i...
Single nucleotide polymorphism (SNP) arrays are powerful tools to delineate genomic aberrations in c...
Tumor single nucleotide polymorphism (SNP) array is a common platform for investigating the cancer g...
Tumor single nucleotide polymorphism (SNP) array is a common platform for investigating the cancer g...
Genomic copy number alteration and allelic imbalance are distinct features of cancer cells, and rece...
Abstract Background Genomic instability in cancer leads to abnormal genome copy number alterations (...
Accurate identification of copy number alterations is an essential step in understanding the events ...
<div><p>Background</p><p>Tumor single nucleotide polymorphism (SNP) array is a common platform for i...
Array-based genotyping platforms have during recent years been established as a valuable tool for th...
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...
BACKGROUND: Using whole exome sequencing to predict aberrations in tumours is a cost effective alter...
The application of genome-wide approaches to the molecular characterization of cancer was investigat...
International audienceIn clinical cancer research, high throughput genomic technologies are increasi...
Abstract Background Genomic aberrations can be used to determine cancer diagnosis and prognosis. Cli...
AbstractIn clinical cancer research, high throughput genomic technologies are increasingly used to i...
Single nucleotide polymorphism (SNP) arrays are powerful tools to delineate genomic aberrations in c...
Tumor single nucleotide polymorphism (SNP) array is a common platform for investigating the cancer g...
Tumor single nucleotide polymorphism (SNP) array is a common platform for investigating the cancer g...
Genomic copy number alteration and allelic imbalance are distinct features of cancer cells, and rece...
Abstract Background Genomic instability in cancer leads to abnormal genome copy number alterations (...
Accurate identification of copy number alterations is an essential step in understanding the events ...
<div><p>Background</p><p>Tumor single nucleotide polymorphism (SNP) array is a common platform for i...
Array-based genotyping platforms have during recent years been established as a valuable tool for th...