An ASHG Interactive Invited Workshop is an educational or instructional event that relates to scientific scholarship, research tools, new technologies, skill development, or public information related to science.
These interactive workshops are being scheduled outside of the annual meeting and do not require a meeting registration to attend. They are ticketed events.
Not an ASHG member? Join or renew your membership before registering to save up to 80% off the ticketed price!
New: When you buy a ticket for any of our January workshop, you will receive a discount code* via email to gain free access to one of our on-demand workshops from September 2021.
*One code per user, not per purchase.
If you are a World Bank Member (Tiers 1 and 2) please do not purchase a ticket. Instead, use the discount code sent to your email or contact email@example.com to get help with registering.
Upcoming January Workshops
- Contains 1 Component(s) Includes a Live Web Event on 01/19/2022 at 12:00 PM (EST)
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.
- Contains 1 Component(s) Includes a Live Web Event on 01/24/2022 at 12:00 PM (EST)
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.
- Contains 3 Component(s) Includes a Live Web Event on 01/26/2022 at 12:00 PM (EST)
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.
- Contains 1 Component(s) Includes a Live Web Event on 01/31/2022 at 12:00 PM (EST)
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.
Upcoming January Workshop Bundle
- Contains 4 Product(s)
This bundle is for upcoming January workshops - buy access to all 4 workshops for the price of 3!
- Contains 1 Component(s)
This workshop will introduce you to powerful metadata searches for the Sequence Read Archive (SRA) by using interactive metadata queries in the cloud.
Analyzing and visualizing single-cell genomics data from the BRAIN Initiative with the Neuroscience Multi-Omic Archive and NeMO Analytics
In this interactive workshop, we will introduce participants to tools for accessing, analyzing, and visualizing BICCN data using the Neuroscience Multi-Omic Archive, which serves as the primary repository for genomics data from the BRAIN Initiative.
An overview of public resources for gene-disease association and sequence and copy number variant interpretation
In this workshop, participants will learn about (and have hands-on experience with) new or newly updated resources that can aid in the interpretation of genomic data.
Open Targets Genetics: An open access resource to systematically prioritize genes at all human GWAS trait-associated loci
In this workshop, we will present Open Targets Genetics, an open access resource which makes robust connections between GWAS-associated loci and likely causal genes, to enable the identification of new drug targets.
- Contains 4 Product(s)
These workshops are on-demand - buy access to all 4 workshops for the price of 3!
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