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EnsembleCNV: an ensemble machine learning algorithm to identify and genotype copy number variation using SNP array data
The associations between diseases/traits and copy number variants (CNVs) have not been systematically investigated in genome-wide association studies (GWASs), primarily due to a lack of robust and accurate tools for CNV genotyping. Herein, we propose a novel ensemble learning framework, ensembleCNV,...
| Autores principales: | , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468244/ https://www.ncbi.nlm.nih.gov/pubmed/30722045 http://dx.doi.org/10.1093/nar/gkz068 |