Predicting the clinical impact of human mutation with deep neural networks
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/s41588-018-0167-z.pdf
Reference92 articles.
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4. Rehm, H. L. Evolving health care through personal genomics. Nat. Rev. Genet. 18, 259–267 (2017).
5. Richards, S. et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet. Med. 17, 405–424 (2015).
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