July 27, 11 a.m. – 1 p.m., virtual
This is a flipped class; links to PowerPoint slides, lecture videos, and practice exercises that you can view on your own schedule are available upon registration.
You’re invited to join the LabArchives Education Edition Bootcamp! During these special training sessions, you’ll learn everything you need to know to prepare for the Fall semester. Join us to learn how the LabArchives Education Edition can help you and your peers to easily manage student lab work and course content – whether your courses are online, in-person, or hybrid.
The Human Gene Mutation Database (HGMD) Professional 2022.2 is now available, expanding the world’s largest collection of human inherited disease mutations to 368,587 entries—that’s 6,354 more than the previous release.
Register to access HGMD with an HSLS license.
SnapGene Academy is SnapGene’s online molecular biology and cloning training platform. Sign up for a free account. SnapGene Academy contains hours of learning material taught by scientific experts about molecular biology and cloning concepts and in-depth tutorials on the tools and features in SnapGene.
The Resource Identification Portal offers a central location for obtaining and exploring Research Resource Identifiers (RRIDs) – unique identifiers for referencing a research resource. If you are an author, please find your key resources: Antibodies, Model Organisms, Cell Lines, Plasmids, and other Tools (software, databases, services).
The PITT CTSI Biostatistics, Epidemiology, and Research Design (BERD) Core offers free walk-in office hours every Friday from 12:00 p.m. to 1:00 p.m. where statisticians are available to answer questions. This is an ideal way to get quantitative input for research projects.
MANE is a collaboration between the National Center for Biotechnology Information (NCBI) and the European Molecular Biology Laboratories-European Bioinformatics Institute (EMBL-EBI).
Are you wondering about the quality of a human, mouse or rat genome that you have assembled?
We offer a new service for evaluating the completeness, correctness, and base accuracy of your human, mouse or rat genome assembly compared to a reference assembly.