A Unified Clinical Genomics Database - ppt video online download
The TP53 Website - TP53 Database
Clinical sequencing: From raw data to diagnosis with lifetime value - Caspar - 2018 - Clinical Genetics - Wiley Online Library
HuVarBase: A human variant database with comprehensive information at gene and protein levels | PLOS ONE
Overview of the Clinical NGS database. This database software was... | Download Scientific Diagram
The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting | SpringerLink
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer | Nature Genetics
The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting | SpringerLink
Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation – topic of research paper in Biological sciences. Download scholarly article PDF and read
DECIPHER v11.12: Mapping the clinical genome
Simple ClinVar internal workflow and main module. (A) Information flow... | Download Scientific Diagram
Frontiers | A Review of Precision Oncology Knowledgebases for Determining the Clinical Actionability of Genetic Variants | Cell and Developmental Biology
Public variant databases: liability? | Genetics in Medicine
DisGeNET - a database of gene-disease associations
Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer - The Journal of Molecular Diagnostics
ClinGen — The Clinical Genome Resource | NEJM
ClinVar - ClinGen | Clinical Genome Resource
Technical desiderata for the integration of genomic data with clinical decision support - ScienceDirect
Using dbSNP and ClinVar to Classify Gene Variants
Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants | Genome Medicine | Full Text
InSiGHT variants databases - InSiGHT
Variation Viewer
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer | Nature Genetics
