Clinical interpretation: when is a variant a mutation? - Genomics Education Programme
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 Interpretation Analysis - OpenCGA - OpenCB
Clinical Organizations Release SARS-CoV-2 Variant Sequencing Guidelines | Today's Clinical Lab
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC ...
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
Comparison of Open-access Databases for Clinical Variant Interpretation in Cancer: A Case Study of MDS/AML | Cancer Genomics & Proteomics
What Is a Variant of Uncertain Significance in Genetic Testing? - European Urology Focus
Stepwise ABC system for classification of any type of genetic variant | European Journal of Human Genetics
Stepwise evidence pipeline for clinical interpretation genetic... | Download Scientific Diagram
Clinical information can lead to finding a variant that might otherwise be missed - Blueprint Genetics
About Us - ClinGen | Clinical Genome Resource
Best practices for the interpretation and reporting of clinical whole genome sequencing | npj Genomic Medicine
Clinical Variant Analysis for Cancer: Part IV | The Golden Helix Blog
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice - ScienceDirect
v1.4.51 Release Notes | CVA Documentation
Clinical Interpretation Analysis - OpenCGA - OpenCB
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
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer | Nature Genetics
Presentation - Variant Classification using ACMG/AMP Guidelines (Steven Harrison) - YouTube
Assessing Variants in a Known Gene: Clinical Variant Classification and Use of the ClinGen Variant Curation Interface - ClinGen | Clinical Genome Resource
ClinGen — The Clinical Genome Resource | NEJM
