Presentation - Variant Classification using ACMG/AMP Guidelines (Steven Harrison) - YouTube
IJMS | Free Full-Text | Consolidated BRCA1/2 Variant Interpretation by MH BRCA Correlates with Predicted PARP Inhibitor Efficacy Association by MH Guide
ClinGen — The Clinical Genome Resource | NEJM
Clinical interpretation: when is a variant a mutation? - Genomics Education Programme
The ClinGen Sequence Variant Interpretation Working Group: Refining Criteria for Interpreting the Pathogenicity of Genetic Variants -
The Clinical Genome (ClinGen) Resource
Best practices for the interpretation and reporting of clinical whole genome sequencing | npj Genomic Medicine
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 Interpretation Analysis - OpenCGA - OpenCB
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice - ScienceDirect
Assessing Variants in a Known Gene: Clinical Variant Classification and Use of the ClinGen Variant Curation Interface - ClinGen | Clinical Genome Resource
Clinical Variant Analysis for Cancer: Part IV | The Golden Helix Blog
Schematic view of the clinical variant interpretation process. In a... | Download Scientific Diagram
Dr. Christine Stanley: Face2Gene LABS at WuXi NextCODE: Phenotyping for Improved Variant Prioritization - FDNA™
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
Clinical Variant Analysis for Cancer: Part IV | The Golden Helix Blog
Nothing's for sure, that's for sure: Evaluating variants of uncertain significance | Beyond the Ion Channel
Genomic Variant Analysis & Clinical Interpretation
About Us - ClinGen | Clinical Genome Resource
Comparison of Open-access Databases for Clinical Variant Interpretation in Cancer: A Case Study of MDS/AML | Cancer Genomics & Proteomics
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 DNA Variant Interpretation: Theory and Practice (Translational and Applied Genomics): 9780128205198: Medicine & Health Science Books @ Amazon.com
Genes | Free Full-Text | Imprecise Medicine: BRCA2 Variants of Uncertain Significance (VUS), the Challenges and Benefits to Integrate a Functional Assay Workflow with Clinical Decision Rules
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer | Nature Genetics
Clinical Organizations Release SARS-CoV-2 Variant Sequencing Guidelines | Today's Clinical Lab
Clinical information can lead to finding a variant that might otherwise be missed - Blueprint Genetics
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
