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      Genomenon and Nostos Genomics Partner to Accelerate Rare Genetic Disease Diagnoses

      Nostos Genomics Integrates Mastermind Genomic Search Engine into AION Variant Interpretation Platform


      News provided by

      Genomenon

      Jun 01, 2021, 00:00 ET

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      Genomenon
      Genomenon

      ANN ARBOR, Mich., June 1, 2021 /PRNewswire-PRWeb/ -- Genomenon® announced a partnership with Nostos Genomics, which includes integration of the Mastermind® Genomic Search Engine cloud-based AION variant interpretation platform. This integration will allow users of AION to preview the number of published articles related to their search and easily link out to view the evidence in Mastermind.

      Leveraging genetic data and clinical evidence is the key to improving the diagnosis of rare diseases and making informed decisions with confidence. This integration of virtually all relevant literature into the genomic analysis process will empower clinical decision-makers to both maximize and act on profound insights contained in next generation sequencing data.

      "This collaboration stemmed from a shared desire to not only provide clinicians with the best decision support possible, but also improve the accuracy, speed, and accessibility of genetic testing to lessen the burden of the diagnostic odyssey for patients."

      Post this

      Mastermind connects patient genetic data with relevant evidence from scientific literature - an essential component of precision medicine for cancer and genetic disease. Using an AI-driven algorithm to index the full text of millions of genomic research articles, Mastermind has created a comprehensive database of over 7 million published variants across all genes and gene elements, updated on a weekly basis.

      This innovative technology has positioned Mastermind as the world's most comprehensive source for genomic literature in the variant interpretation space. Now integrated into over 20 clinical-grade decision support platforms across the globe, Mastermind has quickly become an ideal research companion for those tasked with decoding genomic data.

      Nostos Genomics' AION platform enhances genetic variant interpretation for clinical genetic testing by leveraging AI and functional genomics. Their white-box approach allows users to access a regularly updated knowledge repository with more than 100 annotations, including a selection of data from high-throughput functional genomics assays that directly reflect the molecular impact of thousands of selected mutations.

      "This collaboration stemmed from a shared desire to not only provide clinicians with the best decision support possible, but also improve the accuracy, speed, and accessibility of genetic testing to lessen the burden of the diagnostic odyssey for patients," said David Gorgan, CEO of Nostos Genomics. "The synergy of AION with Mastermind represents an exciting development for this important work."

      "We're excited to partner with Nostos Genomics to put the most comprehensive and up-to-date genomic research in the hands of geneticists and researchers to accelerate rare disease diagnosis," said Mike Klein, CEO of Genomenon. "Our relationship extends Mastermind's global reach and connecting Mastermind with AION provides significant value in cutting turnaround time and increasing diagnostic yield for genetic testing labs."

      About Genomenon

      Genomenon is an AI-driven genomics company that organizes the world's genomic knowledge to connect patient DNA to scientific research in the diagnosis and development of treatments for patients with rare genetic diseases and cancer.

      Genomenon was named Global Company of the Year in Clinical Genomics Interpretation by Frost & Sullivan.

      For more information, visit Genomenon.com

      About Nostos Genomics

      Nostos Genomics is a company engaged in the AI-driven deciphering of genetic diseases, translating genetic information into impactful clinical interventions. Its genetic variant interpretation platform AION leverages a combination of machine learning and functional genomics to characterize mutations and automate the interpretation.

      For more information, visit: nostos-genomics.com

      Media Contact

      Candace Chapman, Genomenon, 734-219-5175, chapman@genomenon.com

      Ansgar Lange, Nostos Genomics, +491775437014, ansgar.lange@nostos-genomics.com

      SOURCE Genomenon

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