Workshop report: the clinical application of data from multiplex assays of variant effect (MAVEs), 12 July 2023
Eur J Hum Genet
.
2024 Mar 4.
doi: 10.1038/s41431-024-01566-2.
Online ahead of print.
Authors
Sophie Allen
1
,
Alice Garrett
2
3
,
Lara Muffley
4
5
,
Shawn Fayer
4
,
Julia Foreman
6
,
David J Adams
7
,
Matthew Hurles
7
,
Alan F Rubin
8
9
,
Frederick P Roth
10
11
12
,
Lea M Starita
4
5
,
Leslie G Biesecker
13
,
Clare Turnbull
2
14
Affiliations
1
Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK. sophie.allen@icr.ac.uk.
2
Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
3
St George's University Hospitals NHS Foundation Trust, Tooting, London, UK.
4
Department of Genome Sciences, University of Washington, Seattle, WA, USA.
5
Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.
6
European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
7
Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
8
Bioinformatics Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
9
Department of Medical Biology, University of Melbourne, Melbourne, VIC, Australia.
10
Department of Computational and Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
11
Donnelly Centre and Departments of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
12
Lunenfeld-Tanenbaum Research Institute, Sinai Health, Toronto, ON, Canada.
13
Center for Precision Health Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
14
The Royal Marsden NHS Foundation Trust, London, UK.
PMID:
38433264
DOI:
10.1038/s41431-024-01566-2
No abstract available
Grants and funding
R01 HL164675/HL/NHLBI NIH HHS/United States
R01 HG013025/HG/NHGRI NIH HHS/United States