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| Funder | NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH |
|---|---|
| Recipient Organization | University of North Carolina Chapel Hill |
| Country | United States |
| Start Date | Sep 20, 2024 |
| End Date | Jun 30, 2028 |
| Duration | 1,379 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 10986275 |
ABSTRACT Clinical virology is predicated on the workflow of analyzing small sample volumes (to minimize patient discomfort, storage, and fit legacy infrastructure) for a single analyte, i.e., virus, with utmost precision. The human virome project (HVP) does not share these restrictions. The HVP priority tissues of urine, stool, saliva, and blood can
be acquired from healthy people in a 50 – 500 ml sample size. For instance, the Red Cross makes normal plasma available in 500 ml bags, and NGS allows for the characterization of all human viruses in a single reaction. This proposal responds to RFA-RM-23-018 with the development of two novel tools: AIM 1, a virus
purification pipeline that utilizes larger volumes to achieve < 1 genome copy/ ml sensitivity; AIM 2, a single virion detection pipeline to provide an accurate denominator of how many intact virions a given NGS sequence set is representing. We hypothesize that Viral Direct Counts (VDC) akin to bacterial direct counts will become the
essential parameter for integrating the studies in the HVP.
University of North Carolina Chapel Hill
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