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Personalised analytics for rare disease diagnostics
oleh: Denise Anderson, Gareth Baynam, Jenefer M. Blackwell, Timo Lassmann
Format: | Article |
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Diterbitkan: | Nature Portfolio 2019-11-01 |
Deskripsi
Genome sequencing is being widely adopted for diagnosis of genetic diseases, but identifying the causal variants remains challenging. Here, the authors introduce a tool that incorporates tissue-specific gene expression data into predicting variant pathogenicity, improving accuracy.