Ambry Genetics Unveils at ASHG New Insights on the Use of Multiomic Testing in 43,000 Patient Study

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Key findings from this study indicate that RNA-dependent classifications were instrumental in enhancing the accuracy of genetic testing.

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Retrieved on: 
Saturday, November 4, 2023
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Science, Biotechnology, Research, Oncology, General Health, Health, Genetics, Clinical Trials, ASHG, Patient, Cancer, VUS, Genetic testing, Ambiguity, Health equity, RNA, JAMA, Society, Genome, Database, Disease, Classification, American Society of Human Genetics, Medicine, Biology, Human genetics, JAMA Oncology, DNA, Vaccine, Pharmaceutical industry
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CALIFORNIA, UNITED STATES, NORTH AMERICA
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AMBRY GENETICS
Summary
Key Points: 
  • Key findings from this study indicate that RNA-dependent classifications were instrumental in enhancing the accuracy of genetic testing.
  • Reducing Inconclusive Rates: The number of variants of uncertain significance reduced considerably, providing clarity and enhancing the overall reliability of multi-gene panel testing.
  • Patients and the healthcare teams who care for them deserve nothing less,” said CEO of Ambry Genetics, Tom Schoenherr.
  • It is a leader in genetic testing that aims to improve health by understanding the relationship between genetics and disease.


Ambry Genetics, a prominent leader in clinical genomic testing and a subsidiary of REALM IDx, Inc., unveiled at the American Society of Human Genetics (ASHG) annual meeting results of a study published in JAMA Oncology that assessed the cumulative impact of paired DNA and RNA testing on detecting disease-causing germline genetic variants and resolution of variants of uncertain significance (VUS).

Key findings from this study indicate that RNA-dependent classifications were instrumental in enhancing the accuracy of genetic testing. Specifically, RNA sequencing played a pivotal role in:

  • Improving Diagnostic Yield: Simultaneous RNA sequencing resulted in a significant increase in the diagnostic yield, providing more accurate and actionable information for individuals undergoing germline cancer predisposition testing.
  • Reducing Inconclusive Rates: The number of variants of uncertain significance reduced considerably, providing clarity and enhancing the overall reliability of multi-gene panel testing.
  • Improving Health Equity: Genetic cohorts are typically derived from European populations, resulting in evidence gaps in underrepresented populations. Generating novel functional evidence helps close those gaps via preferential improvement in VUS rates in non-white populations.

Furthermore, the study revealed that RNA sequencing had a significant impact on the classification of splicing variants. Specifically:

  • Classification of 17.1% of Pathogenic Splicing Variants Dependent on RNA evidence: 17.1% of splicing variants classified as pathogenic would have been classified as variants of uncertain significance without RNA evidence and would therefore not have been clinically actionable.
  • 71.1% of Splicing Variants of Uncertain Significance (VUS) Resolved as Benign: RNA sequencing resolved 71.1% of splicing variants initially categorized as VUS, reducing ambiguity and enhancing the accuracy of hereditary cancer testing.

These findings signify a shift in the field of cancer predisposition, particularly towards the utilization of multiomics genetic testing, providing individuals with more reliable and actionable information, without sacrificing turnaround time. This technology enables healthcare providers to support their patients in making personalized, timely, evidenced-based medical management decisions. As the field of genetic testing continues to evolve, RNA sequencing promises to play a pivotal role in advancing precision medicine.

"The integration of DNA with RNA sequencing into germline cancer predisposition evaluation is the new gold standard for genetic testing,” states Rachid Karam, M.D., Ph.D., VP of Research & Development at Ambry Genetics and lead investigator of this study. “We’ve witnessed a remarkable improvement in diagnostic accuracy and a substantial reduction in inconclusive results. Patients benefit from having access to the most comprehensive genetic testing possible, as demonstrated by the thousands of individuals impacted by RNA testing in our laboratory cohort alone.”

Building upon multiple peer-reviewed publications, Ambry Genetics continues to demonstrate the cumulative impact of RNA sequencing on genetic testing for hereditary cancer predisposition. This innovative approach increases the positive or diagnostic yield, meaning the number of individuals identified with a disease-causing genetic alteration, while simultaneously reducing the inconclusive rate of genetic testing.

“Ambry Genetics has a long history of firsts in the genetic testing space. We stay ahead of the market shifts. We innovate and provide the highest quality genetic testing while championing transparent data sharing to push the industry forward. Patients and the healthcare teams who care for them deserve nothing less,” said CEO of Ambry Genetics, Tom Schoenherr.

ABOUT AMBRY GENETICS ®

Ambry Genetics, a subsidiary of REALM IDx, Inc., translates scientific research into clinically actionable test results based upon a deep understanding of the human genome and the biology behind genetic disease. It is a leader in genetic testing that aims to improve health by understanding the relationship between genetics and disease. Its unparalleled track record of discoveries over 20 years, and growing database that continues to expand in collaboration with academic, corporate and pharmaceutical partners, means Ambry Genetics is first to market with innovative products and comprehensive analysis that enable clinicians to confidently inform patient health decisions.

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