Novel statistical methods and tools to integrate multiple endophenotypes and functional annotation data to study the roles of rare variants in complex human diseases using sequencing data

Registered study from NIH RePORTER funded projects. Evidence status: source reported.

Organisation

Yale University

Published

2020-06-01

Source reference

R01GM134005

Jurisdiction

United States

Licence

Public domain (US Government work, NIH RePORTER). Investigator names are not imported.

Recipient: Yale University (United States) · Funder: NIH NIGMS · Awarded: US$1,620,737 · FY2020 to FY2023 · Found via: UK Biobank

Source: https://reporter.nih.gov/project-details/10631039. Captured 2026-10-30.

Limitations: An NIH award whose title, abstract or indexed terms mention UK Biobank. A mention at funding is not evidence that the data was obtained or analysed; no access agreement is linked by this. The award total is the sum of NIH's yearly award amounts for the fiscal years found, in US dollars, and may include work unrelated to UK data.