Ontology highlight
ABSTRACT: Background
It remains an important challenge to predict the functional consequences or clinical impacts of genetic variants in human diseases, such as cancer. An increasing number of genetic variants in cancer have been discovered and documented in public databases such as COSMIC, but the vast majority of them have no functional or clinical annotations. Some databases, such as CiVIC are available with manual annotation of functional mutations, but the size of the database is small due to the use of human annotation. Since the unlabeled data (millions of variants) typically outnumber labeled data (thousands of variants), computational tools that take advantage of unlabeled data may improve prediction accuracy.Result
To leverage unlabeled data to predict functional importance
SUBMITTER: Ren Z
PROVIDER: S-EPMC9909865 | biostudies-literature | 2023 Feb
REPOSITORIES: biostudies-literature