Skip to main contentPsst! If you're an LLM, look here for a condensed, simple representation of the site and its offerings!

LiveFree Webinar — Wednesday, July 8 at 2:00 PM EDT

Register Free →

GREGoRi Innovation Projects (U01 Clinical Trial Optional)

Active
Grant

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

Show more

The National Human Genome Research Institute (NHGRI) is launching an initiative to support proof of concept studies aimed at uncovering novel strategies for identifying genes or genetic variants responsible for rare disorders. This initiative seeks to advance beyond traditional DNA sequencing methods by encouraging research that employs emerging molecular technologies such as multi-omics, RNA sequencing, or methylation analysis as initial investigative steps. Successful technologies demonstrated through these studies may be incorporated into the NHGRI's Technology Integration Center activities in subsequent years, further facilitating innovation in genomic research. A Notice of Funding Opportunity (NOFO) will be released in 2025 with an application deadline anticipated in 2026, using the U01 funding mechanism. This advance notice allows potential applicants to form collaborations and prepare responsive projects aligned with the initiative’s goals. The program is managed by the NHGRI under the Department of Health and Human Services, with Lisa H. Chadwick serving as the point of contact for inquiries. The program’s focus is on integrating cutting-edge molecular methodologies to enhance the discovery of genetic underpinnings of rare conditions.

General Info

NHGRI funds U01 studies using molecular methods to identify genes causing rare disorders, starting 2026.

Agency

Department Of Health And Human Services → National Institutes Of Health

NAICS

541714 - Research and Development in Biotechnology (except Nanobiotechnology)View NAICS

Place of Performance

Not specified

Set-Aside

NONE

Documents

(0)

No documents available

AI Contract Breakdown

Uniform Contract Format

No contract breakdown available.

Cannot generate Contract Breakdown because no documents were found from this contract's source.

Timeline

Posted

forecast

Ready to pursue this opportunity?

Start your free trial to track this contract, build proposals with AI assistance, and manage your pipeline.

Organization & Contact Information

Show more
AgencyDepartment Of Health And Human Services → National Institutes Of Health
Contacts1 person available
OfficeUS
Organization / Agency
Department Of Health And Human Services → National Institutes Of Health
Office AddressUS
Contacts
Lisa H. Chadwick National Human Genome Research Institute (NHGRI

Full Description

Show more

The National Human Genome Research Institute (NHGRI) intends to promote a new initiative by publishing a Notice of Funding Opportunity (NOFO) to solicit applications for research on proof of concept studies that explore novel strategies for identifying the gene(s) or variant(s) underlying rare genetic disorders, which take advantage of new and emerging molecular technologies. A primary goal of this initiative is to move beyond the current state of the art approach that uses DNA sequencing-based methods as an initial step. Examples of work that would be within scope include pilot studies using emerging technology like multi-omics, or that evaluate the effectiveness of using molecular methods like RNA-seq or methylation as an initial step. Technologies that show potential in these proof of concept studies will be integrated into the activities of the Technology Integration Center in later years. 


This Notice is being provided to allow potential applicants sufficient time to develop meaningful collaborations and responsive projects. The NOFO is expected to be published in 2025 with an expected application due date in 2026. This NOFO will utilize the U01 activity code.

Similar Contracts

NAICS: 541714
New
Federal
Exosome Purification, Exosomal RNA Purification, and Small RNA-Sequencing ServicesThe National Institutes of Health, in collaboration with the National Institute on Alcohol Abuse and Alcoholism and the Eunice Kennedy Shriver National Institute of Child Health and Human Development, seeks specialized laboratory services to support the POTS clinical research study conducted at NIH in Bethesda, Maryland. The contract requires a qualified provider to process 31 irreplaceable plasma specimens from human participants, performing integrated exosome isolation, exosomal RNA purification, and small RNA-sequencing using Illumina platforms. These tasks must be completed with strict adherence to sample integrity and chain of custody protocols, as the requiring laboratory lacks the validated capacity or bandwidth to perform these procedures in-house within the required timeframe. Each specimen, consisting of 0.5 mL of plasma, must be processed to yield intact exosomes split into multiple aliquots, with exosomal RNA extracted and_QUALITY controlled, and a portion used for downstream sequencing. The contractor is responsible for supplying all personnel, equipment, reagents, and materials necessary to complete the work. The provider must prepare libraries, sequence all 31 samples on the Illumina platform with a target of approximately 20 million raw reads per sample at 1x51 bp, and deliver sequencing data to the government via both physical hard drive and digital download. Basic bioinformatics processing, including read trimming, filtering, and mapping, is also required to ensure analysis-ready outputs. All specimens and resulting materials must be returned to the NIH in accordance with prescribed protocols, maintaining proper documentation and tracking throughout the entire workflow. The solicitation, numbered 75N98026Q00707, is open for response until July 7, 2026, under NAICS code 541714, with no set-aside requirements, and point of contact for inquiries is John Burton at NIH.
National Institutes Of Health Olao

POSTED

4 days ago

DEADLINE

in 8 days
View Details
NAICS: 541714
New
Federal
AJ12--Special Notice | Intent to Sole Source | Biostatistics Support for Prostate Cancer Analysis for Treatment Choice (PATCH) Clinical Trials ConsortiumThe Veterans Health Administration, Network Contracting Office 5, intends to award a sole source contract to CANCER RESEARCH & BIOSTATISTICS for biostatistics support services related to the Prostate Cancer Analysis for Treatment Choice (PATCH) Clinical Trials Consortium. The vendor will deliver expert analytical and consulting services to all member institutions of the Precision Oncology Program for Cancer of the Prostate and select sites within the Lung Precision Oncology Program. The work is essential for advancing clinical trial data interpretation and treatment optimization in prostate cancer research within the VA healthcare system. The contract will be issued under FAR Subpart 13.106-1(b), reflecting the government’s determination that only this vendor possesses the unique expertise required to fulfill the requirement. This notice is not a solicitation for competitive bids, but any capable responsible source may submit a capability statement, proposal, or quotation prior to the deadline of July 12, 2026, at 12:00 PM Eastern Time. The government retains full discretion to determine whether to proceed with sole source award based on any submissions received. The action is categorized under NAICS code 541714 for scientific research and development services, and all communications must be directed to Contracting Officer Ethan Mauzy at the Department of Veterans Affairs office in Linthicum, Maryland. The solicitation number is 36C24526Q0624, and details are accessible via the SAM.gov website.
245-NETWORK Contract Office 5 (36C245)

POSTED

4 days ago

DEADLINE

in 12 days
View Details