Family-based SNP analysis for genotype comparison and inheritance exploration
-
Updated
Aug 21, 2026 - HTML
#
variant-interpretation
Here are 5 public repositories matching this topic...
Oncology-focused variant prioritization pipeline for VEP-annotated VCF files derived from clinical NGS data.
-
Updated
Mar 4, 2026 - HTML
Multi-modal AI agent skill and interactive HTML5/WebGL dashboard workbench for quantifying, visualizing, and interpreting regulatory consequences of human genetic variants across 11 molecular modalities.
python webgl bioinformatics transcription-factors deep-learning genomics computational-biology data-visualization gene-regulation molecular-biology precision-medicine epigenomics dna-sequence-analysis variant-interpretation splicing acmg-guidelines interactive-dashboard agent-skill in-silico-mutagenesis genomic-browser
-
Updated
Sep 8, 2026 - HTML
Cancer genomics analysis using OncoKB and clinical somatic variant knowledge bases
-
Updated
Aug 21, 2026 - HTML
Standardized, provenance-tracked context-graph objects for multi-omic biology - the substrate purpose-specific 'omic' models need. Validated on RYR1 variant-to-structure-and-function interpretation (malignant hyperthermia). Built with Claude Code + Claude Science.
bioinformatics structural-biology cryo-em ion-channel claude variant-interpretation multi-omic context-graph ryr1 malignant-hyperthermia
-
Updated
Aug 5, 2026 - HTML
Add this topic to your repo
To associate your repository with the variant-interpretation topic, visit your repo's landing page and select "manage topics."