GenomeArc specializes in providing comprehensive bioinformatics solutions for genomic medicine, offering tools for ultra-fast variant interpretation and clinical decision support. The company's Horizon platform integrates large genomic databases and uses advanced algorithms for rapid and accurate analysis of genomic data. They focus on aiding diagnosis, therapeutic intervention, and research in areas such as cancer and rare genetic diseases.
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To resolve VUS variants, Horizon Variant Knowledgebase provides global open access to additional insights with identical variants. Search your VUS (SNV, Indel, SVs) to gain more insights:https://lnkd.in/dDc-WtM3#VUS #rarediseases #Genome #Gene ...
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📍 We are thrilled to share the complete launch of our Horizon Variant Search platform specifically for rare disease and oncology genomics community. For rare disease and oncology, variant interpretation continues to be a significant obstacle in clinical genomics, particularly as datasets expand concerning SNVs, Indels, and structural variants.Search you germline or somatic variant pathogenicity (ACMG/AMP): https://lnkd.in/dDc-WtM3The server's updated release is built to support researchers and ...
進行中🧬 Advancing clinical genomic interpretation, one platform, one workflow.Genomic data in a clinical setting requires accuracy, context, and consistency across workflows.Horizon Platform v2.3.0 brings together oncology and rare disease interpretation into a single, end-to-end platform designed to support clinical teams with structured, clinical guideline-driven insights.👉 Discover Horizon in action. Request a demo:https://lnkd.in/gre8TY6G🔬 Key capabilities include:🧪 AMP-guided somatic variant ...
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