Featuring Dr. Nikhil Sahajpal of Greenwood Genetic Center, exploring how optical genome mapping (OGM) and long-read sequencing (LRS) are transforming rare disease diagnostics and uncovering previously missed genetic variants.
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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.
#385 Inside ACMG 2026: How AI and New Tools Enhance Genome Sequencing and Equity
See how tools like long read sequencing, RNA sequencing, MAVEs, and AI are ethically transforming WGS to make patients lives better.
#370 Genetics Wrapped: 2025 Top Advances in Genomic Medicine
Drs. Eric Green and Sarah Tishkoff join our host Kira Dineen for our annual recap and reflection on the biggest genetics/genomics advancements this year!