Fabric Genomics possesses deep genomics expertise to help your lab quickly launch and scale NGS testing. We work with many labs that are transitioning to genomics, including labs that don’t yet have in-house NGS experience.
Fabric Genomics is the leading provider of interpretation software for genomic testing, providing best-in-class interpretation software. We can start with raw data from the sequencer (FASTQs) or VCFs to seamlessly generate clinical reports. Further, Fabric Enterprise delivers automated ACMG-compliant classification powered by ACE—Fabric’s AI variant Classification Engine—as well as known variant knowledgebases, so you can generate physician-ready, customized clinical reports.
For labs looking to quickly launch hereditary cancer testing, Fabric’s clinical reporting works out of the box with any panel, including the Illumina TruSight Cancer panel as well as custom panels. Fabric Genomics’ flexible software allows panels to be defined in minutes, including virtual, or in silico, panels where a subset of genes in the wet lab assay are reported on. This flexibility allows a lab to run multiple tests off of a single wet lab assay, from a BRCA1/2 test to a comprehensive cancer panel.
Fabric Genomics works closely with partners to enable the successful launch of your NGS testing:
- Clinical lab set up, accreditation, and test validation
- Laboratory Information Management Systems
- Clinical Services for interpretation and sign-out