Clinically Relevant Variants Resource - Erin Ramos
Identifying Clinically Relevant Variants and Creating Customized Reports
Locus Reference Genomic (LRG) resource
An Introduction to Resources Facilitating Cancer Variant Interpretation
GM4: NHGRI Clinically Relevant Genomic Variants Initiatives - Erin Ramos
Exploring Human Disease and Protein Variant Data in UniProtKB and ProtVar
Maximize your variant knowledge using the Human Gene Mutation Database (HGMD®) Professional
GGMC Expanding Skills Series: "The Clinical Genome Resource (ClinGen)"
MPG Primer: Clinical Variation and Gene Classification (2024)
Evaluating the Clinical Significance of Cytogenomic Variants
StrateGene and MTHFR
MPG Primer: Clinical interpretation of genes and variants for disease causality (2022)
Cancer resources and tools utilizing the Human Disease Ontology
Clinical applications of the Human Disease Ontology
What is Agentic RAG?
Curation of Variants Associated with Pediatric Tumors Within the Clinical Genome Resource
Advancing Genomic Medicine Through Collaboration on a Global Scale with Prof Heidi Rehm (April 2023)
Using metafeature clustering to mine tissue-specific signals from rare variants in the cancer genome
Finding literature for variant interpretation
‘GRN-ACADEMY' - ESS, Module 1 - Topic 2 - Clinically relevant Sinonasal Anatomy - Dr Timothy Beale