<scp>CANVAR</scp>: A Tool for Clinical Annotation of Variants Using <scp>ClinVar</scp> Databases
CANVAR contributes to enhancing variant annotation by offering comprehensive information from the latest ClinVar database for genetic variants identified through next-generation sequencing.
Authors
- Estrid Høgdall (ORCID: https://orcid.org/0000-0003-4689-5658)
- Lau K. Vestergaard (ORCID: https://orcid.org/0000-0002-4750-4877)
- Joanna Lopacinska‐Jørgensen (ORCID: https://orcid.org/0000-0001-7803-425X)
Institutions
- University of Copenhagen (DK)
- Herlev Hospital (DK)
Publication Details
- Journal
- Molecular Genetics & Genomic Medicine
- Published
- 2024-10-01
- DOI
- https://doi.org/10.1002/mgg3.70020
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00