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Active NON-SBIR/STTR RPGS NIH (US)

Additional Sequencing for the Alzheimer Disease Sequencing Project (ADSP) the Follow-Up Study (FUS), The Diverse Population Initiative

$69.42M USD

Funder NATIONAL INSTITUTE ON AGING
Recipient Organization University of Miami School of Medicine
Country United States
Start Date Sep 01, 2022
End Date Aug 31, 2027
Duration 1,825 days
Number of Grantees 5
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 10689971
Grant Description

ABSTRACT The Alzheimer’s Disease Sequencing Project (ADSP) is a national sequencing initiative focused on identifying genetic risk factors for AD. The project’s discovery phase includes whole exome sequencing (WES) of 10,061 unrelated non-White Hispanic individuals of European ancestry (NHW-EA) cases (N=5,096) and controls

(N=4,965), and whole genome sequencing (WGS) of 584 NHW and Hispanic/Latino (HL) familial samples. The 'Discovery Extension Phase' of the project added WGS on ~430 additional familial samples. The ADSP Follow- Up Study 1.0 (ADSP-FUS 1.0) Phase focused on examining candidate variants from the discovery phase, and

identification of novel variants through combined analysis of diverse datasets, is ongoing. Its aim is to sequence existing cohorts with unrelated AD cases that 'encompass the richest possible ethnic diversity' as well as highly valuable set of autopsy confirmed cases and controls. In total we have already included in FUS over 50,000

samples for sequencing including >4,700 autopsy confirmed cases and controls, >9,400 HL ancestry cases and controls and > 8,300 African Ancestry (AA) cases and controls. In this ADSP-FUS 2.0 application, which focuses on the PAR-21-212 goal to increase diversity cohorts in the ADSP with WGS, we are proposing sequencing,

QC and phenotype harmonization of an additional ~16,000 individuals (~12,000 HL ancestry, 500 autopsied NHW-EA, ~3,400 AA and ~170 Asian ancestry individuals) that will both increase our power to find effects and will also enhance our ability to find genetic effects in underserved groups. Additionally, these datasets will

become an invaluable resource for the AD research community at-large.

All Grantees

University of Miami School of Medicine

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