In this webinar recording, Dr. Bryce Daines, VP of Products at Tute Genomics, demonstrates how the Tute Genomics platform, in conjunction with partnering technologies, addresses NGS informatics challenges for clinical genomics.
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Webinar Abstract
As the clinical utility of next-generation sequencing is increasingly proven, strategic opportunities abound for commercial diagnostic laboratories and health systems to offer new, life changing tests to their patient populations. The most significant barrier to widespread adoption and scalability of regulated clinical sequencing however, remains the challenge of building and supporting the informatics infrastructure.
Informatics, if not properly resourced and made accessible to a broader team, can negatively impact everything from the development and validation of new tests, to the interpretation of genomic variants and timely issuance of actionable reports, to the growth of test volumes and expansion of test menus.
In this webinar, Dr. Bryce Daines, VP of Products at Tute Genomics, demonstrates how the Tute Genomics platform, in conjunction with partnering technologies, addresses these challenges.
You will learn how to:
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Generate high quality variant calls using best-practice sequence alignment and variant calling pipelines.
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Verify that genes of interest are adequately captured by targeted sequencing applications, ensuring relevant variants are not inadvertently missed.
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Annotate variants with clinically actionable informationspecific to your patient population.
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Prioritize variants for review and select variants for reporting based on sound logic.
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Produce clear, relevant and timely clinical reports , which include accurate and actionable information for ordering physicians.
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Integrate with leading LIMS and EMR systems .
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Automate and scale your custom-designed, fully integrated informatics, interpretation, and reporting solution for every test (gene panel, exome, and whole genome) and at any volume required.
