Summary: CGHnormaliter is a package for normalization of array comparative genomic hybridization (aCGH) data. It uses an iterative procedure that effectively eliminates the influence of imbalanced copy numbers. This leads to a more reliable assessment of copy number alterations (CNAs). CGHnormaliter is integrated in the Bioconductor environment allowing a smooth link to visualization tools and further data analysis. Availability and Implementation: The CGHnormaliter package is implemented in R and under GPL 3.0 license available at Bioconductor: http://www.bioconductor.org. Contact: heringa@few.vu.nl. © The Author 2010. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjourn...
Contains fulltext : 51763.pdf ( ) (Open Access)BACKGROUND: Currently, two main tec...
Background: In two-channel competitive genomic hybridization microarray experiments...
Copyright © 2011 Jeffrey C. Miecznikowski et al. This is an open access article distributed under th...
Background: Array comparative genomic hybridization (aCGH) is a popular technique for detection of g...
Abstract Background Array comparative genomic hybridization (aCGH) is a popular technique for detect...
BACKGROUND: Array CGH (Comparative Genomic Hybridisation) is a molecular cytogenetic technique for t...
Background Array CGH (Comparative Genomic Hybridisation) is a molecular cytogenetic technique for th...
Copy number alterations (CNAs) in genomic DNA have been associated with complex human diseases, incl...
The robust identification and comprehensive profiling of copy number alterations (CNAs) is highly ch...
Assessing variations in DNA copy number is crucial for understanding constitutional or somatic disea...
Description Normalization and centralization of array comparative genomic hybridiza-tion (aCGH) data...
International audienceAlthough Next Generation Sequencing technologies are becoming the new referenc...
Motivation: Genomic instability is one of the fundamental factors in tumorigenesis and tumor progres...
Summary: CNVDetector is a program for locating copy number varia-tions in a single genome. CNVDetect...
Background. Array-based comparative genomic hybridization (array-CGH) is an emerging high-resolution...
Contains fulltext : 51763.pdf ( ) (Open Access)BACKGROUND: Currently, two main tec...
Background: In two-channel competitive genomic hybridization microarray experiments...
Copyright © 2011 Jeffrey C. Miecznikowski et al. This is an open access article distributed under th...
Background: Array comparative genomic hybridization (aCGH) is a popular technique for detection of g...
Abstract Background Array comparative genomic hybridization (aCGH) is a popular technique for detect...
BACKGROUND: Array CGH (Comparative Genomic Hybridisation) is a molecular cytogenetic technique for t...
Background Array CGH (Comparative Genomic Hybridisation) is a molecular cytogenetic technique for th...
Copy number alterations (CNAs) in genomic DNA have been associated with complex human diseases, incl...
The robust identification and comprehensive profiling of copy number alterations (CNAs) is highly ch...
Assessing variations in DNA copy number is crucial for understanding constitutional or somatic disea...
Description Normalization and centralization of array comparative genomic hybridiza-tion (aCGH) data...
International audienceAlthough Next Generation Sequencing technologies are becoming the new referenc...
Motivation: Genomic instability is one of the fundamental factors in tumorigenesis and tumor progres...
Summary: CNVDetector is a program for locating copy number varia-tions in a single genome. CNVDetect...
Background. Array-based comparative genomic hybridization (array-CGH) is an emerging high-resolution...
Contains fulltext : 51763.pdf ( ) (Open Access)BACKGROUND: Currently, two main tec...
Background: In two-channel competitive genomic hybridization microarray experiments...
Copyright © 2011 Jeffrey C. Miecznikowski et al. This is an open access article distributed under th...