Genome International Corporation – Genomics | Data Analysis | Clinical Research_Education & Science

MENUMENUGenome ExplorerResearchInformation TechnologyAbout UsGet in Touch Genome ExplorerFeaturesActionable decisionApplications in real worldDECODING TO DISCOVEROur mission is to empower hospitals and researchers around the globe to uncover clinically relevant information within the genome, to close the gap from bench to bedside and improve the lives of patients worldwide. Hospitals Diagnostic Labs Researchers Hospitals Diagnostic Labs Researchers Meet Genome Explorer®Your genomic analysis and clinical decision support platform SEQUENCING TO DECISION SUPPORT Our end-to-end genomics facility supports multiple NGS platforms and library strategies with high standard quality control and a fast turnaround time. Genome Explorer® provides clinical insights and superior interpretation. INTELLIGENT WORKFLOW Customized objective-driven workflows support all NGS experimental strategies with intelligent secondary and tertiary genomic analysis. The interpretations are based on our scientifically-validated proprietary algorithms and from our integrated knowledge base. EMPOWERING PRECISION MEDICINE Across our portfolio of products, services, customizable pipelines and reports, Genome Explorer provides clinical decision support tools, revealing crucial information about druggable genes, adverse drug reactions, clinical trials, and more. OUR PROPRIETARY TECHNOLOGIES Our Position Weight Matrix (PWM) splice site detection algorithm is used in clinical and research institutions around the world to discover deleterious mutations in splice junctions, and predict their outcomes in disease-causing genes. Researchers use the algorithm to pinpoint the genetic effects of splice site mutations such as exon skipping and cryptic splice site activation. The algorithm has been cited in over 3,000 research articles that aim to locate splice site mutations in human genes, and determine the underlying causes of cancer and numerous other genetic disorders. GET THE POWER OF THE GENOME IN THE PALM OF YOUR HANDLearn MoreCancer Diagnosis and TherapeuticsIdentify somatic and germline mutations, Gene Fusion events, CNVs and Structural Variants. Transforms tumor DNA to a clinical report in accordance with NCCN, ASCO & ESMO guidelines with FDA approved drugs, dosage, drug adverse effects and relevant clinical trials.Inherited DisordersSequence and discover genetic germline candidate mutations from various Mendelian disorders with inbuilt standard inherited disorder panels. The significant mutations are reported in accordance with ACMG/AMP guidelines and have up-to-date information from all relevant annotation sources.Clients & PartnersUnited States8000 Excelsior Drive, Ste. 202, Madison, Wisconsin [email protected] Genome ExplorerResearchInformation TechnologyAbout UsCareersTerms & Conditions© 2022. Genome International Corp. All Rights Reserved.