Alabama Genomic Health Initiative (AGHI)

Collaboration with Hudson-Alpha The Alabama Genomic Health Initiative is one of the nation's first statewide efforts to harness the power of genomic analysis in helping identify those who are at risk for diseases for genomic abnormalities.

Learn More about AGHI

AGHI Leadership includes members from UAB, HudsonAlpha Institute for Biotechnology and Tuskegee University, nationally recognized institutions that are leaders in bioethics and genomic medicine. Need assistance? ResearchData@uabmc.edu

Data2Discovery Special Interest Group

SIGs Available for Assistance with External Networks

The Data2Discovery Special Interest Groups highlights a number of resources and services for analysis and use of patient data, including several external research enclaves.

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National Clinical Cohort Collaborative (N3C)

A national resource of real-world data that researchers are using to speed medical research A national resource of real-world data that researchers are using to speed medical research

With stewardship from NCATS, more than 90 institutions worked together to build N3C. N3C systematically collects electronic health record (EHR) data from different institutions and harmonizes them into a central enclave. The enclave offers spaces for collaborative research. In addition, EHR data within the enclave can connect to other data sets, which creates a more complete picture of patients’ health journeys.

Visit N3C Website

Need assistance? ResearchData@uabmc.edu

NCATS ENACT

The NCATS ENACT Network, which stands for 'Evolve to Next-Gen ACT' Network, is a platform that allows researchers to query de-identified electronic health record (EHR) data across a consortium of institutions.

Request Access via Email

OneFlorida+ (PCORNet)

The National Patient-Centered Clinical Research Network OneFlorida+ is a collaboration among researchers, clinicians and patients that provides a venue for pragmatic clinical trials, comparative effectiveness research, implementation science studies, observational research, and cohort discovery for a wide range of research. OneFlorida+ is part of the National Patient Centered Clinical Research Network.

Visit OneFlorida Website

Need assistance? Research

Data@uabmc.edu

OneFlorida+ Clinical Research Network
Prep to Research Data Query
Research Application Process

The All of Us Research Network

One of the largest biomedical data resources of its kind.

The All of Us Research Program is a large-scale study that aims to improve health by gathering data from a diverse group of people in the United States. The program is part of the National Institutes of Health's (NIH) Precision Medicine Initiative.

Visit the All of Us Website

Trial Innovation Network (TIN)

Multi-Site Trial Support

The Trial Innovation Network (TIN) is a platform for multi-center trials and studies that encompass a wide-range of disciplines.

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Visit the main site for the Trail Innovation Network

The Trial Innovation Network (TIN) is a platform for multi-center trials and studies that encompass a wide-range of disciplines. Investigators do not need to apply for a specific RFA, but should propose a multi-center trial or study. The Network will prioritize proposals for multi-center clinical trials and studies with patient-oriented endpoints with potential for impact on clinical practice and operational innovation as well as proposals that foster collaborations with other NIH ICs over proposals seeking funding from NCATS.

TriNetX

TriNetX Research datasets provide researchers access to de-identified patient data from a network of health care organizations. TriNetX datasets include clinical patient data such as demographics, diagnoses, procedures, labs and medications - commonly referred to as real-world data.

Request Access via Email

Need assistance? ResearchData@uabmc.edu

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