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PMID: 16434445 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Computation of recurrent minimal genomic alterations from array-CGH data.

Bioinformatics (Oxford, England) ·Vol. 22 ·No. 7 ·2006-04-01 ·Pages 849-56

Rouveirol C, Stransky N, Hupé P, Rosa PL, Viara E, Barillot E, Radvanyi F

Abstract

The identification of recurrent genomic alterations can provide insight into the initiation and progression of genetic diseases, such as cancer. Array-CGH can identify chromosomal regions that have been gained or lost, with a resolution of approximately 1 mb, for the cutting-edge techniques. The extraction of discrete profiles from raw array-CGH data has been studied extensively, but subsequent steps in the analysis require flexible, efficient algorithms, particularly if the number of available profiles exceeds a few tens or the number of array probes exceeds a few thousands. We propose two algorithms for computing minimal and minimal constrained regions of gain and loss from discretized CGH profiles. The second of these algorithms can handle additional constraints describing relevant regions of copy number change. We have validated these algorithms on two public array-CGH datasets. From the authors, upon request. celine@lri.fr Supplementary data are available at Bioinformatics online.

MeSH Terms
Algorithms Breast Neoplasms/genetics,metabolism Chromosome Mapping Colonic Neoplasms/genetics,metabolism Computer Simulation Databases, Genetic Female Gene Expression Profiling/methods Humans Neoplasms/genetics,metabolism Oligonucleotide Array Sequence Analysis/methods Reproducibility of Results
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Rouveirol C
LRI, UMR CNRS 8623, Université Paris Sud, bât 490 91405 Orsay cedex, France. celine@lri.fr
Stransky N
Hupé Ph
Rosa Ph La
Viara E
Barillot E
Radvanyi F
Article Info
Journal
Bioinformatics (Oxford, England)
Abbr.
Bioinformatics
ISSN
1367-4803
Published
2006-04-01
Epub
2006-00-24
Pages
849-56
Language
English
Region
England
NLM ID
9808944
Subset
IM
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