IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variants.
By Carolin Knecht, Matthew E. Mort, O. Junge, David N. Cooper, M. Krawczak, A. Caliebe. 2016
14 citations recorded by the source corpus.
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- Philipp Rentzsch
- Martin Kircher
- Daniela M. Witten
- Jay Shendure
- Gregory M. Cooper
- Max Schubach
- Tommaso Cai
- Xueqiu Jian
Citations in the corpus
- CADD: predicting the deleteriousness of variants throughout the human genome (2018, positive): “Some recently developed predictors are ensemble learners, which combine CADD and other scores (38–41).”
- The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies (2017, unknown): “2015), IMHOTEP (Knecht et al. 2017) and M-CAP (Jagadeesh et al.”