Session description:
Explore kidney disease genomics with NephQTL, a comprehensive eQTL/CRE portal. In this session you will uncover how genomic variants regulate specific genes using high-resolution data for precise gene-mapping.
Learning objectives:
- Access eQTLs derived from glomerular and tubulointerstitial samples from the NEPTUNE Nephrotic Syndrome observational study patient cohort.
- Learn how to leverage kidney single-nucleus open chromatin data for enhanced eQTL accuracy.
- Navigate the interactive search through eQTLs, snATAC-seq tracks, snRNA-seq counts, and single-cell deltaSVM scores.
- Finally, dive into validated variants and genes demonstrated by the experimental models accessible in the software.
Click here to sign up for the Big Data Lab Session: https://events.theisn.org/wcn25/book/bdl