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CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping

Copy number variations (CNVs) are widely known to be an important mediator for diseases and traits. The development of high-throughput sequencing (HTS) technologies has provided great opportunities to identify CNV regions in mammalian genomes. In a typical experiment, millions of short reads obtaine...

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Autori principali: Wang, Zhanyong, Hormozdiari, Farhad, Yang, Wen-Yun, Halperin, Eran, Eskin, Eleazar
Natura: Artigo
Lingua:Inglês
Pubblicazione: Mary Ann Liebert, Inc. 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3590897/
https://ncbi.nlm.nih.gov/pubmed/23421794
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/cmb.2012.0258
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