WEBINAR: MaveDB: discovery and interpretation of high-throughput functional assay data

This record includes training materials associated with the Australian BioCommons webinar ‘MaveDB: discovery and interpretation of high-throughput functional assay data’. This webinar took place on 26 March 2024.
Event description
Multiplexed assays of variant effect (MAVEs) are a family of experimental techniques that measure all single amino acid or single nucleotide changes in a gene or other functional element. MaveDB is an international community database that enables discovery and reuse of data from these experiments. It provides a platform for integrating large-scale measurements of sequence variant impact with applications that can be used to interpret the data for basic and clinical research.
In this webinar we consider: 

What are MAVEs and how are the experiments performed?

How much MAVE data is available in MaveDB and how is it organised?

Who can submit datasets to MaveDB?

What are some of the clinical applications for MAVEs and how is the data being used to understand patient variants?

 
Speaker: Dr Alan Rubin, Senior Research Officer, WEHI 
Host: Dr Melissa Burke, Australian BioCommons
 
Materials
Materials are shared under a Creative Commons Attribution 4.0 International agreement unless otherwise specified and were current at the time of the event.
Files and materials included in this record:

Event metadata (PDF): Information about the event including, description, event URL, learning objectives, prerequisites, technical requirements etc.

Index of training materials (PDF): List and description of all materials associated with this event including the name, format, location and a brief description of each file.

MAVEDB_slides: A PDF copy of the slides presented during the webinar.

Materials shared elsewhere:
A recording of this webinar is available on the Australian BioCommons YouTube Channel: https://youtu.be/BXGQ2IuDnGE