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Detection of common copy number variation with application to population clustering from next generation sequencing data
Copy number variation (CNV) is a structural variation in human genome that has been associated with many complex diseases. In this paper we present a method to detect common copy number variation from next generation sequencing data. First, copy number variations are detected from each individual sa...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4154475/ https://ncbi.nlm.nih.gov/pubmed/23366124 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/EMBC.2012.6346163 |
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