<p><b>Panel A:</b> Graphical whole-genome views of both sample types showing that majority of the copy number aberrations (CNAs) identified in the macro-dissected FFPE sample were not detected in the FF sample. Deletions on the long arms of chromosomes 9, 14 and 15 as well as the short arm of chromosome 16 were the called on both sample types. <b>Panel B:</b> High resolution graphical views of a 6 Mb region along on Chromosome 14 (14q24.1) showing a group of probes with an average log<sub>2</sub> ratio of approximately 0.6 and the corresponding single copy amplification detected in the FFPE sample but no aberrations detected in the FF sample. <b>Panel C:</b> High-resolution graphical views showing a closely similar copy number aberration de...
BACKGROUND: Microarray Comparative Genomic Hybridization (array CGH) provides a means to examine DNA...
Array-CGH is a powerful tool for the rapid detection of genomic imbalances. By customizing the array...
Motivation Existing methods for estimating copy number variations in array comparative genomic hybri...
<p><b>Panel A:</b> Graphical whole-genome views of copy number aberrations (CNAs) identified in both...
<p><b>Panel A:</b> Graphical whole-genome views of copy number aberrations (CNAs) identified in both...
Formalin-fixed, paraffin-embedded (FFPE) archival tissue is an important source of DNA material. The...
Developing effective methods for analyzing array-CGH data to detect chromosomal aberrations is very ...
Array-based comparative genomic hybridization (aCGH) allows measuring DNA copy number at the whole g...
The aim of the study is comparative analysis of algorithms for identifying copy number variation in ...
Background: The accurate and high resolution mapping of DNA copy number aberrations has become an im...
<p>Twelve tumors were analyzed by CGH: ten by cCGH (Panel I, A–J), eight by aCGH (Panel II, B, C, E,...
Background: Array comparative genomic hybridisation (CGH) is a powerful method for the genetic analy...
Large-scale copy number variants (CNVs) have recently been recognized to play a role in human genome...
Recurrent genomic amplications and deletions characterize cancer genomes and contribute to disease ...
Background. Array-based comparative genomic hybridization (array-CGH) is an emerging high-resolution...
BACKGROUND: Microarray Comparative Genomic Hybridization (array CGH) provides a means to examine DNA...
Array-CGH is a powerful tool for the rapid detection of genomic imbalances. By customizing the array...
Motivation Existing methods for estimating copy number variations in array comparative genomic hybri...
<p><b>Panel A:</b> Graphical whole-genome views of copy number aberrations (CNAs) identified in both...
<p><b>Panel A:</b> Graphical whole-genome views of copy number aberrations (CNAs) identified in both...
Formalin-fixed, paraffin-embedded (FFPE) archival tissue is an important source of DNA material. The...
Developing effective methods for analyzing array-CGH data to detect chromosomal aberrations is very ...
Array-based comparative genomic hybridization (aCGH) allows measuring DNA copy number at the whole g...
The aim of the study is comparative analysis of algorithms for identifying copy number variation in ...
Background: The accurate and high resolution mapping of DNA copy number aberrations has become an im...
<p>Twelve tumors were analyzed by CGH: ten by cCGH (Panel I, A–J), eight by aCGH (Panel II, B, C, E,...
Background: Array comparative genomic hybridisation (CGH) is a powerful method for the genetic analy...
Large-scale copy number variants (CNVs) have recently been recognized to play a role in human genome...
Recurrent genomic amplications and deletions characterize cancer genomes and contribute to disease ...
Background. Array-based comparative genomic hybridization (array-CGH) is an emerging high-resolution...
BACKGROUND: Microarray Comparative Genomic Hybridization (array CGH) provides a means to examine DNA...
Array-CGH is a powerful tool for the rapid detection of genomic imbalances. By customizing the array...
Motivation Existing methods for estimating copy number variations in array comparative genomic hybri...