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






