Tumor formation is in part driven by DNA copy number alterations (CNAs), which can be
measured using microarray-based Comparative Genomic Hybridization (aCGH) …

Genetic alterations are a key feature of cancer cells and typically target biological processes
and pathways that contribute to cancer pathogenesis. Array-based comparative genomic …

The development of solid tumors is associated with acquisition of complex genetic
alterations, indicating that failures in the mechanisms that maintain the integrity of the …

Background Most approaches used to find recurrent or differential DNA Copy Number
Alterations (CNA) in array Comparative Genomic Hybridization (aCGH) data from groups of …

Background Array-based comparative genomic hybridization (CGH) is a commonly-used
approach to detect DNA copy number variation in whole genome-wide screens. Several …

Array comparative genomic hybridization (aCGH) is a technique for measuring
chromosomal aberrations in genomic DNA. With the availability of high-resolution …

Alterations in the genome that lead to changes in DNA sequence copy number are a
characteristic of solid tumors and are found in association with developmental abnormalities …

Array-based comparative genomic hybridization (aCGH) is a high-resolution, high-
throughput technique for studying the genetic basis of cancer. The resulting data consist of …

Motivation: Genomic DNA regions are frequently lost or gained during tumor progression.
Array Comparative Genomic Hybridization (array CGH) technology makes it possible to …

Motivation: The identification of DNA copy number changes provides insights that may
advance our understanding of initiation and progression of cancer. Array-based comparative …