HAL (France)open access
eDiVA—Classification and prioritization of pathogenic variants for clinical diagnostics
Whole-exome sequencing, Disease variant prioritization, Machine learning, NGS diagnostics, Rare genetic disease, 0
This document is indexed with metadata only — full text is not available in the archive for this record.
Open the official source ↗
Record · ID 322603
Retrieved via
Conceptio — every document is proof-bundled with source, license, and retrieval metadata.