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Chromatin accessibility prediction via a hybrid deep convolutional neural network
MOTIVATION: A majority of known genetic variants associated with human-inherited diseases lie in non-coding regions that lack adequate interpretation, making it indispensable to systematically discover functional sites at the whole genome level and precisely decipher their implications in a comprehe...
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| Publicado no: | Bioinformatics |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6192215/ https://ncbi.nlm.nih.gov/pubmed/29069282 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx679 |
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