Analysis software Emedgene

testinterpretationscreening

Emedgene variant interpretation software streamlines your tertiary analysis workflows for rare disease genomics and other germline research applications Confidently scale variant analysis with explainable AI (XAI) Emedgene software is designed to accelerate the time and certainty in user-defined variant interpretation, prioritization, curation, and research report generation from sequencing and microarrays. Streamlined Enable greater efficiency from your tertiary analysis workflows with explainable AI (XAI) and automation supporting genomes, exomes, virtual panels, targeted panels, and microarrays. From dozens of samples to populations, save valuable time per subject and per project. Integrated Unify your wet lab and dry lab to simplify and secure your complete sequencing or microarray workflow. Integrate with DRAGEN secondary analysis for accurate, comprehensive, and efficient variant calling. Speed user-driven, variant interpretation by up to 75% per subject from single sample workflows to population scale studies. Powered for growth Confidently keep pace with evolving science, technology, and test volumes with up-to-date knowledge sources, automated curation capabilities, and a team of experts to support your journey.​ We help you Scale volume Increase throughput without increasing headcount using explainable AI (XAI) and automated workflows. Speed user-driven, variant interpretation by up to 75% per subject from single sample workflows to population scale studies. Launch assays Whether you are conducting rare disease or other genetic disease research, hereditary risk assessment, carrier screening, healthy population screening,