Article
Toward trustable use of machine learning models of variant effects in the clinic.
American journal of human genetics - 5 Dec 2024
Dias Mafalda, Orenbuch Rose, Marks Debora S, Frazer Jonathan
Abstract excerpt
There has been considerable progress in building models to predict the effect of missense substitutions in protein-coding genes, fueled in large part by progress in applying deep learning methods to sequence data. These models have the potential to enable clinical variant annotation on a large scale and hence increase the impact of patient sequencing in guiding diagnosis and treatment. To realize this potential,...
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