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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...
This episode belongs to DNA Today: A Genetics Podcast.
Audio availability depends on the podcast feed.
Published May 8, 2026.
Questions About This Episode
What is #393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap about?
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.
Where can I listen to #393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap?
You can listen to #393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap online on Radio and Podcast. Open the player on this page to stream the available audio.
Which podcast is #393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap from?
#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.
How long is this episode?
The episode duration depends on the source podcast feed and may not always be available.
When was this episode published?
This episode was published on May 8, 2026.
Can I save #393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap for later?
Yes. Use the heart button on the episode page to add it to your favorite episodes list.
Are there related episodes from DNA Today: A Genetics Podcast?
Yes. This page shows related episodes from DNA Today: A Genetics Podcast when more episodes are available from the podcast feed.
Quick Answers About This Episode
Where can I listen to #393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap?
You can listen to #393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap on this page when the episode audio is available from the podcast feed.
Which podcast is this episode from?
#393 Whole Genome Sequencing and Multi-omic Tools Closing the Rare Disease Diagnostic Gap is from DNA Today: A Genetics Podcast by Kira Dineen.
What are the episode details?
Published May 8, 2026