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DTSTAMP:20260707T153629Z
UID:481e7292-bf05-43da-9ca3-08340358e3f6
DTSTART:20240326T020000Z
DTEND:20240326T030000Z
DESCRIPTION:Multiplexed assays of variant effect (MAVEs) are a family of ex
 perimental techniques that measure all single amino acid or single nucleot
 ide changes in a gene or other functional element.[ MaveDB](https://www.ma
 vedb.org/#/) is an international community database that enables discovery
  and reuse of data from these experiments. It provides a platform for inte
 grating large-scale measurements of sequence variant impact with applicati
 ons that can be used to interpret the data for basic and clinical research
 .\n\nIn this webinar we consider: \n\n1. What are MAVEs and how are the ex
 periments performed?\n2. How much MAVE data is available in MaveDB and how
  is it organised?\n3. Who can submit datasets to MaveDB?\n4. What are some
  of the clinical applications for MAVEs and how is the data being used to 
 understand patient variants?\n\n**Speaker:** Dr Alan Rubin\, Senior Resear
 ch Officer\, WEHI\n\n**Date/Time:** Tuesday 26 March 2024\,  1 - 2 pm AEDT
 / 12 - 1 pm AEST / 12:30 - 1:30 pm ACDT / 10 - 11 am AWST\n\n**Who the web
 inar is for:**\n\nAnyone with an interest in high-throughput functional as
 says for research or clinical applications. \n\n**How to join:**\n\nThis w
 ebinar is free to join but you must[ register for a place in advance](http
 s://unimelb.zoom.us/webinar/register/WN_1Lxp3KRKTqu39z-YsHnh5w).\n\nA reco
 rding of this webinar will be shared on the Australian BioCommons YouTube 
 channel
SUMMARY:WEBINAR: MaveDB: discovery and interpretation of high-throughput fu
 nctional assay data
URL;VALUE=URI:https://www.biocommons.org.au/events/mavedb
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