Ontology highlight
ABSTRACT:
SUBMITTER: Anderson D
PROVIDER: S-EPMC9313608 | biostudies-literature | 2022 May
REPOSITORIES: biostudies-literature
Anderson Denise D Lassmann Timo T
Human mutation 20220309 5
Identifying the causal variant for diagnosis of genetic diseases is challenging when using next-generation sequencing approaches and variant prioritization tools can assist in this task. These tools provide in silico predictions of variant pathogenicity, however they are agnostic to the disease under study. We previously performed a disease-specific benchmark of 24 such tools to assess how they perform in different disease contexts. We found that the tools themselves show large differences in pe ...[more]