CNstream: A method for the identification and genotyping of copy number polymorphisms using Illumina microarrays

<p>Abstract</p> <p>Background</p> <p>Understanding the genetic basis of disease risk in depth requires an exhaustive knowledge of the types of genetic variation. Very recently, Copy Number Variants (CNVs) have received much attention because of their potential implicati...

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Bibliographic Details
Main Authors: Balsa Alejandro, Ballina Javier, Cañete Juan D, Canaleta Cristina, Tortosa Raül, Julià Antonio, Alonso Arnald, Tornero Jesús, Marsal Sara
Format: Article
Language:English
Published: BMC 2010-05-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/11/264