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Grant Award View - GA176019
Diagnosis, discovery and novel phenotype characterisation using...
GA ID:
GA176019
Agency:
Department of Health and Aged Care
Approval Date:
16-Jun-2021
Publish Date:
5-Jul-2021
Category:
Health and Medical Research
Grant Term:
16-Jun-2021 to 31-May-2025
Value (AUD):
$2,997,450.25
(GST inclusive where applicable)
One-off/Ad hoc:
No
Aggregate Grant Award:
No
PBS Program Name:
DoHAC 20/21 1.1 Health Policy Research and Analysis
Grant Program:
2020_MRFF_Genomics_Health_Futures_Mission _Streams_1-2
Grant Activity:
Diagnosis, discovery and novel phenotype characterisation using multimodal genomics in patients with inherited bone marrow failure and related disorders
Purpose:
This project seeks to identify novel genetic causes of a group of rare diseases called 'inherited bone marrow failure syndromes'. Currently only ~50 percent of cases have a known genetic cause, required for a correct diagnosis, prognosis and for making treatment choices. We will study the genomes of 350 patients with this disease in order to: identify novel causes of these diseases, improve the diagnostic rate, and assess the benefits of providing genomic testing to all patients with this disease.
GO ID:
GO Title:
MRFF - Genomics Health Futures Mission - 2020 Genomics Health Futures Mission Grant Opportunity
Internal Reference ID:
MRF2007548
Selection Process:
Targeted or Restricted Competitive
Confidentiality - Contract:
Yes
Confidentiality Reason(s) - Contract:
Privacy Act 1988
Intellectual property
Intellectual property
Confidentiality - Outputs:
Yes
Confidentiality Reason(s) - Outputs:
Intellectual property
Grant Recipient Details
Recipient Name:
University of Melbourne
Recipient ABN:
84 002 705 224
Grant Recipient Location
Suburb:
Parkville
Town/City:
Parkville
Postcode:
3052
State/Territory:
VIC
Country:
AUSTRALIA
Grant Delivery Location
State/Territory:
NSW, VIC, SA, TAS
Postcode:
Multiple
Country:
AUSTRALIA