Conferences

News & Press

The power and cost-effectiveness of AI are calling into question many of our assumptions about healthcare.   The most important dichotomy proving to be false is that providing the latest and most thorough diagnostic technology to optimize clinical outcomes is more expensive.  When we use AI to more comprehensively analyze cases we benefit from Moore’s law rapidly and continuously reducing costs.  By contrast, hospital-based care, especially when in an intensive setting such as the NICU is continuously increasing in cost. It is not surprising that when more extensive testing produces clinically actionable results that actually decrease hospital costs we can accomplish the holy grail — better and less expensive simultaneously.

Read More

Clinical genomic testing and next-generation sequencing (NGS) are integral parts of realizing the potential of precision medicine, but the data complexity and technical integrations needed to make genomic data clinically meaningful and routinized have slowed mainstream adoption of these breakthrough technologies. Today, Fabric Genomics, a global leader in clinical interpretation of genomic data, announced a distribution agreement with XIFIN, a …

Read More

Researchers at Rady Children’s Institute for Genomic Medicine (RCIGM) and its partners, including Fabric Genomics, have today published in Science Translational Medicine a new study documenting the process to diagnose rare genetic diseases in record time. This new method speeds answers to physicians and allows increased use of genome sequencing as a first-line diagnostic test …

Read More

Fabric Genomics will launch a new solution this week for variant interpretation and clinical reporting, allowing clinical laboratories to dramatically accelerate turnaround times. This new software solution, called Fabric Hereditary Panels with ACE (AI Classification Engine), will debut at the ACMG annual meeting in Seattle, Washington. The solution incorporates an extensively validated, automated ACMG classification …

Read More

Diagnomics, a leading genetic testing company, has developed a new ACMG 59 report that is available to healthcare providers and their patients to complement Diagnomics’ portfolio of Personalized Genomics. Diagnomics has partnered with Fabric Genomics to use Fabric Enterprise, its clinical decision-support platform, to generate clinical insights for the report.

Read More

Fabric Genomics and Genomenon announced today that they have entered into a partnership with the goal of further strengthening clinical genomic interpretation and variant classification. Fabric Genomics speeds and scales genomic interpretation by combining the most advanced AI algorithms with automated workflows, while Genomenon’s literature search engine facilitates comprehensive literature review, which is advantageous for …

Read More

CHICAGO (GenomeWeb) – From the beginning, Fabric Genomics (formerly Omicia) has developed a unique solution for phenotype-driven genome interpretation from whole genome and exome data. The company is expanding into more hospital systems and clinical lab worldwide. “Our goal is to bring this now to every single hospital and every single testing lab around the …

Read More

Fabric Genomics was recently highlighted in the San Francisco Business Times. Martin Reese, CEO, discussed how Fabric is transforming health care with clinical insights through AI interpretations of genomes, exomes, and panels for hereditary diseases and cancer. “We provide the software; the labs provide the genomics data,” said Reese. “We then do machine learning with …

Read More