Industry-leading Variant Interpretation
Robust data interpretation is critical to accurately identify genomic variants and deliver maximum diagnostic yield. Typical genome interpretation methods focus on filtering to identify and prioritize variants. Fabric Enterprise is an artificial intelligence (AI)-driven platform that combines deep phenotype and genotype data, enabling labs to achieve diagnostic yields ~2X compared to the industry standard (~50% vs. 25-30%, respectively). Plus, Fabric Enterprise is always up to date with the latest reference data and standard guidelines to enable accurate variant interpretation and classification.
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Rapid Diagnostic Solutions for Life-changing Interventions
A limiting factor for exome or whole genome sequencing is the time between sample collection and results reported. This turnaround time (TAT) is influenced by multiple factors, including diagnostic methodology and on-site resources.
Fabric Enterprise is an all-in-one platform for secondary analysis, interpretation, and reporting. Fabric Enterprise employs proven AI-driven prioritization to deliver a rapid TAT from VCF data to clinical results.
Fast, AI-driven analysis greatly reduces the amount of time needed to analyze each case, allowing your staff to focus on the most likely causative candidates first -- and report more cases in less time.
Powerful Genomic Interpretation for Children’s Hospitals of All Sizes
Fabric Enterprise is designed to support all NGS-based diagnostic tests regardless of test type or scale. Starting from either raw data or variant calls from whole genome, exome, or panel tests, Fabric Enterprise provides efficient workflows for genome annotation, interpretation, clinical report generation, and sign-off. And Fabric’s scalable cloud solution incorporates comprehensive data and network security protocols.