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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

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

Toronto, Canada 🇨🇦

Doly Begum is ready to build a stronger, more prosperous, and more independent Canadian economy. Early voting opens today in Scarborough Southwest and Election Day is April 13 — don’t forget to get out and vote.

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

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

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…

Islamophobia has no place in Canada. 9 years ago today, the lives of 6 Canadian Muslims were horrifically taken in an Islamophobic act of terror in Québec City that left 19 more people injured. As we remember them, we remain committed to building a country where Canadians of all faiths can live openly, freely, and safely.

We’re buying Canadian, and we’re building Canadian.

Join us as we host Dr. Nikil Sudarsan for an inspiring talk on how the global genomic revolution is redefining diagnosis and therapeutics in pediatric medicine. Please register for the talk: lnkd.in/djcrWiat #rarediseases #genomics #neuro #mutation #gene #genome

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…

Changing the world by surprise - Quantum computing! Quantum computing powering a new multiverse of solutions. A nice resource & review how quantum computing can implement precision medicine. Paper: nature.com/articles/s4152… #medicine #quantum #physics #genomics

Excited to share our comprehensive review on Quantum Computing and its potential to change biomedicine. This paper provides foundational knowledge of quantum dynamics and resources needed to begin tackling complex problems. nature.com/articles/s4152… #quantumAI #quantumComputing