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Comprehensively benchmarking applications for detecting copy number variation
Motivation: Recently, copy number variation (CNV) has gained considerable interest as a type of genomic variation that plays an important role in complex phenotypes and disease susceptibility. Since a number of CNV detection methods have recently been developed, it is necessary to help investigators...
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| Yayımlandı: | PLoS Comput Biol |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6555534/ https://ncbi.nlm.nih.gov/pubmed/31136576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1007069 |
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