CoNVEX: copy number variation estimation in exome sequencing data using HMM

CoNVEX: copy number variation estimation in exome sequencing data using HMM

<p>Abstract</p> <p>Background</p> <p>One of the main types of genetic variations in cancer is Copy Number Variations (CNV). Whole exome sequenicng (WES) is a popular alternative to whole genome sequencing (WGS) to study disease specific genomic variations. However, find...

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Bibliographic Details
Main Authors:	Amarasinghe Kaushalya C, Li Jason, Halgamuge Saman K
Format:	Article
Language:	English
Published:	BMC 2013-01-01
Series:	BMC Bioinformatics
Subjects:	CNV detection Cancer Genome Targeted resequencing Whole exome sequencing Hidden Markov Models Discrete Wavelet Transform

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