BACKGROUND: Cancer progression is associated with genomic instability and an accumulation of gains and losses of DNA. The growing variety of tools for measuring genomic copy numbers, including various types of array-CGH, SNP arrays and high-throughput sequencing, calls for a coherent framework offering unified and consistent handling of single- and multi-track segmentation problems. In addition, there is a demand for highly computationally efficient segmentation algorithms, due to the emergence of very high density scans of copy number. RESULTS: A comprehensive Bioconductor package for copy number analysis is presented. The package offers a unified framework for single sample, multi-sample and multi-track segmentation and is based on statis...
Motivation: With the expansion of whole-genome studies, there is rapid evolution of genotyping platf...
Abstract Background Variations in DNA copy number carry information on the modalities of genome evol...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Background Cancer progression is associated with genomic instability and an accumula...
Background: Cancer progression is associated with genomic instability and an accumulation of gains a...
Abstract Background Cancer progression is associated with genomic instability and an accumulation of...
A number of bioinformatic or biostatistical methods are available for analyzing DNA copy number prof...
A number of bioinformatic or biostatistical methods are available for analyzing DNA copy number prof...
Background: Variations in DNA copy number carry information on the modalities of genome evolution an...
Abstract Background Variation in DNA copy number, due to gains and losses of chromosome segments, is...
Received on; revised on; accepted on Motivation: DNA copy number variants (CNV) are gains and losses...
Abstract Background Genome-wide DNA copy number changes are the hallmark events in the initiation an...
<p>Aligned DNA sequences of the tumor specimen are normalized against a process‐matched normal, prod...
International audienceA number of bioinformatic or biostatistical methods are available for analyzin...
We developed Copy Number Segmentation by Regression Tree in Next Generation Sequencing (CONSERTING),...
Motivation: With the expansion of whole-genome studies, there is rapid evolution of genotyping platf...
Abstract Background Variations in DNA copy number carry information on the modalities of genome evol...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...
Background Cancer progression is associated with genomic instability and an accumula...
Background: Cancer progression is associated with genomic instability and an accumulation of gains a...
Abstract Background Cancer progression is associated with genomic instability and an accumulation of...
A number of bioinformatic or biostatistical methods are available for analyzing DNA copy number prof...
A number of bioinformatic or biostatistical methods are available for analyzing DNA copy number prof...
Background: Variations in DNA copy number carry information on the modalities of genome evolution an...
Abstract Background Variation in DNA copy number, due to gains and losses of chromosome segments, is...
Received on; revised on; accepted on Motivation: DNA copy number variants (CNV) are gains and losses...
Abstract Background Genome-wide DNA copy number changes are the hallmark events in the initiation an...
<p>Aligned DNA sequences of the tumor specimen are normalized against a process‐matched normal, prod...
International audienceA number of bioinformatic or biostatistical methods are available for analyzin...
We developed Copy Number Segmentation by Regression Tree in Next Generation Sequencing (CONSERTING),...
Motivation: With the expansion of whole-genome studies, there is rapid evolution of genotyping platf...
Abstract Background Variations in DNA copy number carry information on the modalities of genome evol...
Summary:Copy number variation is an important and abundant source of variation in the human genome, ...