Personalised analytics for rare disease diagnostics

oleh: Denise Anderson, Gareth Baynam, Jenefer M. Blackwell, Timo Lassmann

Format: Article
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.