Genomic data is the key to unlocking the secrets of human health and disease. But analyzing and interpreting genomic data is not easy. It requires advanced tools and expertise that are often not available or affordable for many researchers and clinicians.

Fabric Enterprise is a platform that takes raw data from next-generation sequencing (NGS), and turns it into genomic insights for clinical diagnostics and research. NGS is a technology that can sequence the entire genome or specific regions of interest in a fast and accurate way. NGS can reveal the genetic variations that are associated with rare diseases, hereditary risks, and cancer.

But NGS data alone is not enough. You need to analyze and interpret the data to make sense of it and use it for clinical decision making. That’s where Fabric Enterprise comes in. Fabric Enterprise delivers NGS data analysis and clinical reporting for hereditary panels, somatic cancer panels, and whole genomes. Fabric Enterprise uses artificial intelligence (AI) to provide best-in-class accuracy and scalability for NGS analysis.

Fabric Enterprise offers the following features and benefits:

  • AI-based platform: Fabric Enterprise uses AI to automate and optimize the analysis and interpretation of NGS data. AI can identify the most relevant variants, genes, and pathways for each case, and provide evidence-based recommendations for diagnosis and treatment.
  • Comprehensive reports: Fabric Enterprise generates clinical reports that are easy to understand and actionable. The reports include the summary of findings, the interpretation of variants, the clinical implications, and the references to support the conclusions.
  • Customizable workflows: Fabric Enterprise allows you to customize your workflows according to your needs and preferences. You can choose from different analysis options, such as variant calling, annotation, filtering, prioritization, classification, and reporting. You can also integrate your own data sources, such as databases, guidelines, or literature.
  • Scalable solution: Fabric Enterprise can handle any volume of NGS data, from single samples to large cohorts. Fabric Enterprise can run on cloud or on-premise environments, depending on your security and performance requirements.
  • Collaborative platform: Fabric Enterprise enables you to collaborate with other users and share your data and reports. You can create teams and projects on Fabric Enterprise and invite other users to join. You can also export your data and reports to other formats or platforms.

Fabric Genomics is the company behind Fabric Enterprise. Fabric Genomics is a leader in AI-based NGS analysis, interpretation, and clinical reporting for rare disease, hereditary risk, and cancer testing. Fabric Genomics has been trusted by dozens of the world’s leading hospitals, clinical labs, and academic centers, such as Cincinnati Children’s, InterMountain, Rady Children’s Institute, LabCorp, and others.

If you are interested in using Fabric Enterprise for your genomic data analysis needs, you visit their website. You can also request a demo or a free trial of Fabric Enterprise on their website.

I hope this blog post has helped you understand how Fabric Enterprise can transform your genomic data into clinical insights. Fabric Enterprise is a powerful and innovative platform that can help you improve your genomic research and diagnostics. Try it today and see the difference! 😊

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