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Computation of recurrent minimal genomic alterations from array-CGH data
Author(s) -
Céline Rouveirol,
Nicolas Stransky,
Philippe Hupé,
Ph. La Rosa,
Eric Viara,
Emmanuel Barillot,
François Radvanyi
Publication year - 2006
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btl004
Subject(s) - computer science , comparative genomic hybridization , identification (biology) , computation , discretization , copy number analysis , algorithm , high resolution , computational biology , copy number variation , biology , genome , genetics , mathematics , mathematical analysis , botany , gene , remote sensing , geology
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.

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