PRESENTATION TITLE
Single Cell Multi-omics Analysis of Pancreatic Islet 

Learning Objectives
Upon completion of this activity, participants should be able to: 

1. Recognize that Pancreatic beta cell function and morphology are highly heterogeneous.
2. Describe type 2 Diabetes (T2D)-associated β-cell heterogeneity at both transcriptomic and epigenomic levels through integration of single-cell transcriptome, single-nuclei chromatin accessibility and cell-type specific 3D genome profiles from human islets.
3. Identify HNF1A as a principal driver for beta cell heterogeneity.
4. Recognize that the in vitro differentiation of insulin-producing beta-like cells is a powerful model for human pancreas development. 

ATTENDANCE / CREDIT
Text the session code (provided only at the session) to 507-200-3010 within 48 hours of the live presentation to record attendance. All learners are encouraged to text attendance regardless of credit needs. This number is only used for receiving text messages related to tracking attendance. Additional tasks to obtain credit may be required based on the specific activity requirements and will be announced accordingly. Swiping your badge will not provide credit; that process is only applicable to meet GME requirements for Residents & Fellows.

TRANSCRIPT
Any credit or attendance awarded from this session will appear on your Transcript.

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