NIH-funded research R21 grant

Developing tools to analyze genetic variations linked to health and disease.

Official title: Creating an advanced multi-ancestral resource and tools for short tandem repeat analysis in the AOURP researcher workbench

Funded at University of Miami School of Medicine · NIH-10798717 · Data updated 2026-11-12

This study is looking at tiny genetic variations in our DNA that can affect our health, using new technology to gather and analyze information from people with different backgrounds, so we can better understand how these variations might help improve diagnoses and treatments for various health issues.

Quick facts

Grant typeR21 grant
Study typeNIH-funded research
Funding institutionUniversity of Miami School of Medicine
NIH-funded
Lab location1 site (Coral Gables, United States)
Project startSeptember 15, 2023
Project endAugust 31, 2025
Funding year2023
Award (this year)$422,125
NIH project number1R21HG013397-01
Project IDNIH-10798717 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research include individuals from various ancestral backgrounds who may have genetic conditions linked to tandem repeats.

Less likely to help

Patients with no known genetic conditions or those not interested in genetic research may not receive direct benefits from this research.

What this research studies

This research focuses on creating advanced resources and analytical tools to study short tandem repeats (TRs) in the human genome, which are variations that can influence health and disease. By utilizing cutting-edge bioinformatics and long-read sequencing technologies, the project aims to analyze a vast dataset of TRs from diverse ancestral backgrounds. Patients may benefit from insights gained about how these genetic variations relate to various health conditions, potentially leading to improved diagnostics and treatments.

Why it matters

Potential benefit: If successful, this research could enhance our understanding of genetic factors influencing health and lead to better disease management for diverse populations.

How similar studies have gone: Previous research has shown promise in analyzing genetic variations using similar bioinformatics approaches, indicating potential for success in this novel investigation.

Where this research is happening

  • University of Miami School of Medicine
    Coral Gables, United States
    Active

Researchers

  • Principal investigator: Danzi, Matthew Christopher — University of Miami School of Medicine
  • Study coordinator: Danzi, Matthew Christopher

Related research

Other NIH-funded projects on the same topics.

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    NIH research University of Miami School of Medicine · Coral Gables, United States · NIH-11607100

  • Understanding the Genetics Behind IBD in South Florida

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  • MorpHiC Data Resource and Coordinating Center

    A national effort to build and share a comprehensive, high-quality catalogue of how human genes affect cell function when they’re turned off, using human cellular models.

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  • MorPhiC data hub for gene function in human cells

    A data resource and coordinating center will organize and share information about how human genes affect cellular traits when knocked out, helping researchers understand gene functions.

    NIH research University of Miami School of Medicine · Coral Gables, United States · NIH-11599437

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.