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CLAMMS: a scalable algorithm for calling common and rare copy number variants from exome sequencing data
Motivation: Several algorithms exist for detecting copy number variants (CNVs) from human exome sequencing read depth, but previous tools have not been well suited for large population studies on the order of tens or hundreds of thousands of exomes. Their limitations include being difficult to integ...
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| 發表在: | Bioinformatics |
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| Main Authors: | , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4681995/ https://ncbi.nlm.nih.gov/pubmed/26382196 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv547 |
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