A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer | Nature Genetics
Genomic Variant Analysis & Clinical Interpretation
Risk of severe clinical outcomes among persons with SARS-CoV-2 infection with differing levels of vaccination during widespread Omicron (B.1.1.529) and Delta (B.1.617.2) variant circulation in Northern California: A retrospective cohort study -
Clinical Variant Analysis for Cancer: Part IV | The Golden Helix Blog
Clinical interpretation: when is a variant a mutation? - Genomics Education Programme
The Clinical Genome (ClinGen) Resource
Schematic view of the clinical variant interpretation process. In a... | Download Scientific Diagram
Nothing's for sure, that's for sure: Evaluating variants of uncertain significance | Beyond the Ion Channel
Clinical Interpretation Analysis - OpenCGA - OpenCB
Clinical Interpretation Analysis - OpenCGA - OpenCB
Comparison of Open-access Databases for Clinical Variant Interpretation in Cancer: A Case Study of MDS/AML | Cancer Genomics & Proteomics
ClinGen — The Clinical Genome Resource | NEJM
Best practices for the interpretation and reporting of clinical whole genome sequencing | npj Genomic Medicine
Clinical Organizations Release SARS-CoV-2 Variant Sequencing Guidelines | Today's Clinical Lab
Introduction to Genomic Variant Interpretation for Clinicians - YouTube
Clinical Variant Classification: A Comparison of Public Databases and a Commercial Testing Laboratory. | Semantic Scholar
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice - ScienceDirect
Stepwise evidence pipeline for clinical interpretation genetic... | Download Scientific Diagram
IJMS | Free Full-Text | Consolidated BRCA1/2 Variant Interpretation by MH BRCA Correlates with Predicted PARP Inhibitor Efficacy Association by MH Guide
Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype‐weighted knowledge in the CAGI SickKids5 clinical genomes challenge - Pal - 2020 - Human Mutation - Wiley Online Library
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice - ScienceDirect
Genomic Variant Analysis & Clinical Interpretation | Council of Scientific & Industrial Research | CSIR | GoI
