Accelerating the Identification of Genetic Diseases

Life Sciences, Healthcare, Laboratory Technology,
  • Monday, October 19, 2020

Realizing the potential of precision medicine relies on accurate and efficient diagnoses. However, even less complex NGS cases can take experts 12 hours to analyze – adding over $500 of costs to every analysis. Alongside this, 71% of clinical laboratories report that they are nearly or completely at capacity. Increasing case throughput and reducing interpretation time are therefore essential.

In this webinar, the panelist will demonstrate how Congenica Automation can enable complex genomic data interpretation, including classification, evidence and reporting in as little as five minutes.



Helen Savage, DipRCPath, Deputy Head of Clinical Services, Congenica

Helen Savage is a Clinical Scientist with 12 years’ experience working in the NHS and biotech industry. She is skilled in variant interpretation across rare disease and cancer, feeding her clinical experience into product management in Congenica, to develop a best-in-class software solution for the analysis and interpretation of genetic data for patients with rare disease.

Message Presenter

Who Should Attend?

This webinar is relevant to personnel with the following job titles:

  • Clinical Scientists
  • Clinical Geneticists
  • Genomic data analysts
  • Laboratory managers
  • Genetic counselors
  • Heads of diagnostics
  • Directors of diagnostics
  • Diagnostics managers
  • Molecular diagnostic scientists

Working in:

  • Genetic/Genomic Analysis & Interpretation
  • Genetic Testing
  • Molecular Pathology
  • Molecular Diagnostics
  • Genome Sequencing

What You Will Learn

Join us for this webinar to discover:

  • How to maximize case throughput using curated variant lists
  • Methods to reliably automate genomic analysis with confidence and transparency
  • How to interpret and report a case in as little as 5 minutes

Xtalks Partner


Congenica are a digital health company enabling genomic medicine with the world’s leading clinical decision support platform for the rapid analysis and interpretation of genomic data.

Built on a foundation of clinical expertise, we are driven to empower healthcare professionals worldwide to transform health and wellness, improving lives by converting genomic data into actionable information.

Our platform can analyze the entire human genome, to not only find the problem but go further, collect a wealth of information, trillions of data points, then interpret and understand every detail.

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