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An accurate and powerful method for copy number variation detection
MOTIVATION: Integration of multiple genetic sources for copy number variation detection (CNV) is a powerful approach to improve the identification of variants associated with complex traits. Although it has been shown that the widely used change point based methods can increase statistical power to...
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| Publicado no: | Bioinformatics |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6735918/ https://ncbi.nlm.nih.gov/pubmed/30649252 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty1041 |
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