GenomeArc

Today we launched variant.genomearc.com a variant interpretation knowledge-base server, for rare diseases and cancer. Get variant ACMG/AMP insights and pharmacogenomic details for actionability. Enjoy browsing Horizon. #genome #genomics #wholegenome

Search any variant to learn about their ACMG or AMP pathogenicity for #raredisease or #cancer This is free to use, and includes SNV, indels, and SVs, with non-coding annotations as well. Horizon variant search server: variant.genomearc.com #rarediseases #cancer #genome #VUS

Search your somatic variants to learn AMP Tier classification, drug insights and from additional tumors: -AMP Tier classification -FDA-approved drug insights -Additional supporting tumor data 🚀 Search Your Somatic Variant: lnkd.in/dDc-WtM3 #cancer #tumor #somatic

Type your SNV or Structural Variant (SV) to learn pathogenicity, germline or somatic. Interpreting SVs remains a great challenge in clinical #genomics. Excited to share a global variant insight resource (following ACMG and AMP guidelines), search variant: variant.genomearc.com

Variant interpretation for rare disease and cancer, free to use with global access. #raredisease #cancer #genome Article: communities.springernature.com/posts/unlockin…

Unlocking Genomic Variant Insights: Your Free Resource for Rare Disease (Germline) and Cancer (Somatic) Variants communities.springernature.com/posts/unlockin…

Try Horizon for free: variant.genomearc.com

Excited to share our CNV study, 'Horizon: CNV interpretation through rapid automated ACMG-aligned pathogenicity analysis' #RareDisease #Genetics Here is the paper: link.springer.com/article/10.100… You test your CNV/SV pathogenicity, with free access: variant.genomearc.com

We have released SNV/Indel/SV pathogenicity Analysis Software Horizon. With Horizon, you can get germline and somatic variant insight for free. You can start small clinical genomics project yourself right away in our cloud, without a high-spec server. variant.genomearc.com

Today we launched variant.genomearc.com a variant interpretation knowledge-base server, for rare diseases and cancer. Get variant ACMG/AMP insights and pharmacogenomic details for actionability. Enjoy browsing Horizon. #genome #genomics #wholegenome

Horizon: CNV interpretation through rapid automated ACMG-aligned pathogenicity analysis #RareDisease #Genetics link.springer.com/article/10.100…

Full Paper: nature.com/articles/s4152…

A Paradigm Shift in Medicine About to Start. An exciting paper on quantum computing that outlines a roadmap for how QC may impact the implementation of precision medicine, starting 2026. From genomic diagnosis, single cell to drug design, QC is the future. #quantum #medicine

Excited to share the full version of our paper, designed to help labs launch their first #quantum computing project. We provide foundational quantum knowledge and practical resources to enable quantum computing in precision #medicine. Paper: nature.com/articles/s4152…