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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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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Mary Ann Liebert, Inc.
2013
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| Assuntos: | |
| Acceso en liña: | 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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