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#393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap artwork
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#393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap

DNA Today: A Genetics Podcast by Kira Dineen

Baylor Genetics’ Dr. Christine Eng and Chris Sands explore the power of whole genome sequencing when paired with multi-omic technology, like long-read sequencing, optical genome mapping, and RNA sequencing.

About This Episode

#393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap is an episode from DNA Today: A Genetics Podcast by Kira Dineen. Baylor Genetics’ Dr. Christine Eng and Chris Sands explore the power of whole genome...

Podcast

This episode belongs to DNA Today: A Genetics Podcast.

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Episode Details

Published May 8, 2026.