Improving the use of rapid whole genome sequencing for critically ill newborns in the NICU
Official title: Addressing the research-practice gap in the implementation of rapid whole genome sequencing in the NICU
Funded at University of Utah · NIH-10918215 · Data updated 2026-11-12
This study is working to make sure that quick whole genome sequencing becomes a regular part of care for critically ill newborns in NICUs, especially in rural areas, by finding and fixing any obstacles that get in the way, so that more babies can benefit from this important technology.
Quick facts
| Grant type | Career grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | University of Utah NIH-funded |
| Lab location | 1 site (Salt Lake City, United States) |
| Project start | September 1, 2023 |
| Project end | August 31, 2028 |
| Funding year | 2024 |
| Award (this year) | $269,246 |
| NIH project number | 5K08HG013111-02 |
| Project ID | NIH-10918215 on NIH RePORTER |
Who could benefit from this research
✓Could help
Ideal candidates for this research are critically ill newborns in NICUs, particularly those in rural or lower-resourced areas.
✕Less likely to help
Patients who are not in need of genomic sequencing or those in higher-resourced NICUs where this technology is already implemented may not benefit from this research.
What this research studies
This research focuses on enhancing the implementation of rapid whole genome sequencing as a standard practice for critically ill newborns in neonatal intensive care units (NICUs). It aims to identify and address barriers that prevent the adoption of this life-saving technology, particularly in rural and lower-resourced settings. By developing specific strategies and testing them in real-world settings, the project seeks to ensure that genomic medicine is effectively integrated into clinical care for newborns. The research also includes training for the investigator to become an expert in this field.
Why it matters
Potential benefit: If successful, this research could lead to faster diagnoses and more effective treatments for critically ill newborns, ultimately saving lives.
How similar studies have gone: Other research has shown success in implementing genomic medicine in clinical settings, but this specific approach to addressing the research-practice gap is relatively novel.
Where this research is happening
-
University of Utah
Salt Lake City, United States Active
Researchers
- Principal investigator: Malone Jenkins, Sabrina — University of Utah
- Study coordinator: Malone Jenkins, Sabrina
About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page.