Our laboratory scientists and services team assist with assay design and validation, including custom gene panel design, gene curation, configuration of standard operating procedures, software deployment and integration with laboratory information systems.
Our Fabric Enterprise software automates variant calling and variant interpretation, including the incorporation of phenotypic data to streamline conversion of raw genomic data into clinically meaningful and actionable insights.
Our network of ABMGG board-certified & board-eligible professionals and clinical variant scientists provide interpretation and sign out. Our team has broad experience across disease areas, and can enable labs to launch testing quickly while still ramping up staffing, or for long-term needs for interpretation.
A physician-ready clinical report is generated within the Fabric Enterprise software, output either as a lab-branded, professionally formatted PDF or as structured data.