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Joint detection of copy number variations in parent-offspring trios
Motivation: Whole genome sequencing (WGS) of parent-offspring trios is a powerful approach for identifying disease-associated genes via detecting copy number variations (CNVs). Existing approaches, which detect CNVs for each individual in a trio independently, usually yield low-detection accuracy. J...
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| Publicado en: | Bioinformatics |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4907378/ https://ncbi.nlm.nih.gov/pubmed/26644415 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv707 |
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