This bundle is for upcoming January workshops - buy access to all 4 workshops for the price of 3!

This workshop will appeal to researchers and clinicians interested in exploring SV calling with long-read sequencing data, as well as anyone more broadly interested in practical ways to access and analyze data in the cloud - with or without advanced computing training.

Students, postdocs, and scientists in academia and industry who work on population genetics problems can benefit from learning and using the methods introduced in this workshop. Human geneticists and medical researchers who wish to incorporate ancestry and demographic information in studying their trait of interest will find the demographic and ancestry inference part helpful. Statisticians, computer scientists, and those who develop methods could benefit from learning the simulation tools instructed here.

This workshop is ideal scientists who would like to find and use tools in the cloud for genomic analysis. Researchers interested in NHGRI data, such as the Human Pangenome Project, are especially encouraged to attend. Basic knowledge of Python or R is recommended but not required.

The Genome Browser is a valuable tool at all levels of genetics education and research, but this is not an introductory workshop. It is designed to show users who have at least a working familiarity with the Browser new features likely not seen before.

Dr. Hannah Polikowsky discusses their recent HGGA paper.