GenomeArc

🚨 Collaborating to Solve Rare Disease Mysteries 🚨 ☄️ Rare disease cases often remain unresolved, with traditional methods and algorithms failing to provide answers. Variants of Uncertain Significance (VUS) are left behind, leaving patients and families searching for clarity. ☄️ We’re excited to announce the launch of our Global Collaborative Initiative to "Solving the Unresolved" rare disease cases with GenomeArc Horizon™️ multimodal OMICs platform. Together with researchers, clinicians, and diagnostic teams worldwide, we can bring answers to those in need. 📩 Let’s collaborate! Email: [email protected] to join this important effort. More on GenomeArc Horizon™️: https://lnkd.in/dFdgNzXS #RareDiseases #Genomics #CollaborativeScience #GenomeArc #HorizonPlatform

☄️GenomeArc started a global collaboration to help clinicians and scientists to resolve rare disease patients remained undiagnosed with VUS variants. 💫GenomeArc Horizon, a multimodal clinical genomics platform will reanalyze unresolved complex cases to bring variants/genes to enhance diagnosis. 💫Please email us if it interest you: [email protected] Read more about “Redolving the Unresolved”: https://lnkd.in/de7Avzh7 #rarediseases #genomics #raredisease #clinicalgenomics #VUS

At GenomeArc, our mission is to bridge the gap between breakthrough science and meaningful patient impact. GenomeArc Horizon™️ delivers ultra-fast, reproducibly accurate genome tertiary analysis, setting a new standard in the field. One of the most common questions we hear is: "How does GenomeArc Horizon implement its ultra-fast algorithm?" Let’s hear directly from our Founder, Mohammed Uddin Dafil, on how this innovative solution came to life. Learn more about GenomeArc Horizon: https://lnkd.in/dFdgNzXS #GenomeArcHorizon #PrecisionMedicine #Genomics #PatientImpact

Variant frequencies vary between populations due to multiple factors. To identify population-specific variants associated with the risk of various diseases, it is crucial to develop genomic resources tailored to each population. Learn more about genetic diversity of populations: https://lnkd.in/e7bHpvy3 #genetics #populationgenetics #genomics #diversity

Clinical Genomics with GenomeArc Horizon: Are you ready to unlock the power of genomics for rare diseases and cancer? GenomeArc Horizon, a comprehensive clinical genomic solution that empowers healthcare providers to accurately classify pathogenicity for SNVs, Indels, and SVs. Key Features: -Multi-OMICs Integration: Leverage the combined power of genomics, transcriptomics, and proteomics for deeper insights for ACMG guided variant interpretation. -Advanced AI and Machine Learning: Employ cutting-edge AI and machine learning algorithms to enhance variant interpretation. -Large Language Model: Access a wealth of molecular genomics knowledge at your fingertips. With GenomeArc Horizon, you can: -Accelerate diagnosis and treatment plans -Improve patient outcomes Learn more and Request a Demo: https://lnkd.in/dFdgNzXS #genomics #raredisease #cancer #clinicalgenomics #AI #machinelearning #precisionmedicine #healthcare #bioinformatics

✨Towards the first human cell atlas, HCA published 45 papers in Nature and its associated journals. An amazing resource for multi-OMICs communities. ✨Single cell transcriptome is an amazing technology, GenomeArc fully integrated its single cell capabilities with publicly available atlases. ☄️Human Cell Atlas Nature Papers: https://lnkd.in/eCNeb7-Y #SingleCell #transcriptome #Cell

🌟 Exciting Tech Spotlight to Aid You with Genomic Diagnosis! 🌟 🧬 Our Horizon Intelligence – the AI powerhouse embedded within the GenomeArc Horizon™️ Platform, designed to redefine genomic diagnostics. 🧬With dynamic learning capabilities, Horizon Intelligence evolves with every interaction, empowering local genome diagnosis and ensuring seamless alignment with ACMG guidelines. Plus, its natural language-powered search makes finding variants intuitive and efficient, transforming how we navigate complex genomic landscapes. A great aid to resolve variant of uncertain significance (VUS) to enhance diagnostic yield. Ready to experience the future of genomic insights? 🚀 Learn about GenomeArc Horizon multi-OMICs platform for clinical genomics: https://lnkd.in/dFdgNzXS Learn more about Horizon Intelligence and ACMG guided diagnosis: https://lnkd.in/dZ-reK8e #Genomics #AI #PrecisionMedicine #GenomeArcHorizon #HorizonIntelligence

🧬 Tumor profiling just got easier! With GenomeArc Horizon™, you can effortlessly analyze tumor somatic mutational landscapes from VCF files. GenomeArc Horizon™ technology delivers comprehensive tumor profiles in minutes. 🧬 Our cutting-edge algorithm capable of detecting somatic variants at an allele frequency as low as 5%, our technology ensures deep, reliable analysis for comprehensive genomic profiling with pharmacogenomic insights. 🧬 Request a demo on GenomeArc Horizon™ https://lnkd.in/dFdgNzXS #GenomeArcHorizon #TumorProfiling #VCFAnalysis #CancerResearch #Genomics

When I was awarded my first patent at The Hospital for Sick Children, it triggered the thought of bringing technology to the masses. That is when GenomeArc started its humble beginning in Toronto, 🇨🇦. I never thought GenomeArc will achieve this massive accelration in technology development in such a short time. From enabling whole genome variant classification for diagnosis in 10 minutes to helping genomic clinics in three continents, solving thousands of cases! I learned so much from so many of my Canadian colleagues, on talent acquisition to design complex software solutions. There is no failure in a journey where every step is a destination! ✨ #genomics #technology

🌍🧬The World Health Organization’s Genomics Programme has introduced new principles for the ethical collection, access, use, and sharing of human genome data. These guidelines establish a global standard for responsible genomic data practices, created in collaboration with the WHO Technical Advisory Group on Genomics (TAG-G) and international experts. As genomic technologies evolve, having a strong ethical framework is more important than ever.🌍🧬 🌍🧬Genomic Data Sharing WHO Guidelines: https://lnkd.in/dAMkZ-Nf #genomics #WHO