Opportunity Information: Apply for G20AS00136

The Cooperative Ecosystem Studies Unit (CESU) Great Lakes Northern Forests opportunity (Funding Opportunity Number G20AS00136) is a US Geological Survey (USGS) research funding announcement issued by the Department of the Interior through the USGS National Wildlife Health Center. It is a discretionary award made as a cooperative agreement, meaning the project is expected to involve substantial involvement and collaboration with the federal partner during the work. The opportunity falls under the Science and Technology and other Research and Development activity category and is listed under CFDA 15.808. The solicitation was created on August 17, 2020, with an original closing date of August 28, 2020.

The purpose of the project is to evaluate, in a practical and performance-focused way, how sensitive two newer, relatively low-cost next-generation sequencing (NGS) platforms are when used for viral pathogen detection and genome recovery. The work is framed around the need for faster and more accessible sequencing-based diagnostics, especially for emerging pathogens where time-to-answer can directly affect outbreak response and decision-making. Rather than focusing on developing a brand-new technology, the project aims to rigorously characterize what these already-available platforms can reliably detect and assemble under realistic sample conditions, and then convert those findings into standardized methods that other laboratories can quickly adopt.

One major component targets the Oxford Nanopore MinION platform. Nanopore sequencing is highlighted for its ability to stream data in real time, enabling analysis to begin immediately instead of waiting for a run to finish, which can take hours or days on more conventional sequencing systems. Under this award, the recipient is expected to characterize the sensitivity of the MinION for identifying a viral pathogen directly from a sample, with an emphasis on speed, including demonstrating identification in as little as 30 minutes. In practical terms, that sensitivity work typically involves determining the lowest viral quantity and/or lowest fraction of viral material in a background of host or environmental nucleic acids that still produces a confident identification within the desired time window, and documenting the conditions and workflow steps that control that performance.

The second major component focuses on the Illumina iSeq 100 system. The iSeq is positioned as a scaled-down Illumina platform that still provides the high data density associated with Illumina sequencing, but in a format better suited to single, high-value samples rather than high-throughput batch processing. The project will characterize the minimal amount of virus needed in a sample to successfully assemble a whole viral genome using the iSeq 100. This part of the work is about defining the practical threshold where a lab can move from simple detection to full-genome recovery, which is important for downstream uses like strain typing, tracking transmission, and identifying mutations relevant to virulence, host range, or diagnostic escape.

A final set of deliverables is strongly oriented toward implementation and technology transfer. The project will standardize the resulting procedures for both platforms into formal standard operating procedures (SOPs), improve the analytical software used for analyzing data generated by each system, and then disseminate the methods and tools so that other laboratories can adopt them quickly. The announcement specifically references NAHLN labs (the National Animal Health Laboratory Network), signaling that a key goal is operational readiness across a broader lab network, not just a single research demonstration. In other words, the award is meant to produce reproducible, transferable workflows and analysis approaches that reduce guesswork for labs trying to stand up rapid sequencing-based pathogen detection.

In terms of funding structure and scale, the opportunity anticipates a single award with an award ceiling of $386,575. Eligibility is limited to CESU partners under the Great Lakes Northern Forests CESU (the notice lists eligible applicants as "Others" with clarification in the full eligibility text), which generally means only organizations formally participating in that CESU consortium can apply. Overall, the grant supports applied research that benchmarks rapid pathogen identification and whole-genome assembly thresholds on two accessible sequencing platforms, and then turns the results into standardized, shareable protocols and improved analytics to strengthen rapid detection capacity for emerging pathogens.

  • The Department of the Interior, U. S. Geological Survey in the science and technology and other research and development sector is offering a public funding opportunity titled "Cooperative Ecosystem Studies Unit, Great Lakes Northern Forests CESU" and is now available to receive applicants.
  • Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 15.808.
  • This funding opportunity was created on Aug 17, 2020.
  • Applicants must submit their applications by Aug 28, 2020. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
  • Each selected applicant is eligible to receive up to $386,575.00 in funding.
  • The number of recipients for this funding is limited to 1 candidate(s).
  • Eligible applicants include: Others (see text field entitled Additional Information on Eligibility for clarification).
Apply for G20AS00136

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Frequently Asked Questions (FAQs)

What is the name of this funding opportunity?

This opportunity is the Cooperative Ecosystem Studies Unit (CESU) Great Lakes Northern Forests opportunity, Funding Opportunity Number G20AS00136.

Which federal agency is issuing this announcement?

The announcement is issued by the US Geological Survey (USGS) under the Department of the Interior, through the USGS National Wildlife Health Center.

What type of award is being offered?

The award is a discretionary award made as a cooperative agreement. This means the project is expected to involve substantial involvement and collaboration with the federal partner during the work.

What is the overall purpose of the project being funded?

The purpose is to evaluate, in a practical and performance-focused way, how sensitive two newer, relatively low-cost next-generation sequencing (NGS) platforms are for viral pathogen detection and genome recovery. The goal is to characterize what these existing platforms can reliably detect and assemble under realistic sample conditions and turn the findings into standardized methods other laboratories can adopt quickly.

Is this opportunity focused on developing a brand-new sequencing technology?

No. The project is framed around rigorously characterizing the performance of already-available sequencing platforms under realistic conditions, rather than inventing an entirely new technology.

Which sequencing platforms are specifically covered in this project?

The project focuses on two platforms: the Oxford Nanopore MinION and the Illumina iSeq 100.

What is the MinION-related component expected to evaluate?

The MinION component is expected to characterize sensitivity for identifying a viral pathogen directly from a sample, with an emphasis on speed. The announcement highlights demonstrating identification in as little as 30 minutes.

What does "sensitivity" mean in the MinION part of the work (as described in the announcement)?

In practical terms, it typically means determining the lowest viral quantity and/or the lowest fraction of viral material in a background of host or environmental nucleic acids that still produces a confident identification within the desired time window, and documenting the conditions and workflow steps that control performance.

Why is the MinION platform highlighted for speed?

Nanopore sequencing is highlighted because it can stream data in real time, allowing analysis to begin immediately rather than waiting for a sequencing run to finish, which can take hours or days on more conventional systems.

What is the Illumina iSeq 100 component expected to evaluate?

The iSeq 100 component will characterize the minimal amount of virus needed in a sample to successfully assemble a whole viral genome using the iSeq 100.

What is the practical significance of defining a whole-genome assembly threshold?

Defining the threshold helps clarify when a lab can move from simple detection to full-genome recovery. Whole-genome recovery supports downstream uses such as strain typing, tracking transmission, and identifying mutations that may be relevant to virulence, host range, or diagnostic escape.

What implementation or technology-transfer deliverables are expected?

The project is expected to standardize procedures for both platforms into formal standard operating procedures (SOPs), improve the analytical software used to analyze data from each system, and disseminate the methods and tools so other laboratories can adopt them quickly.

Who are the methods and tools intended to help, according to the announcement?

The announcement references NAHLN labs (the National Animal Health Laboratory Network), indicating a key goal is operational readiness across a broader laboratory network, not just a single research demonstration.

What activity category does this opportunity fall under?

The opportunity is under the Science and Technology and other Research and Development activity category.

What CFDA number is associated with this opportunity?

The opportunity is listed under CFDA 15.808.

How many awards are anticipated?

The opportunity anticipates a single award.

What is the maximum funding amount (award ceiling) for this opportunity?

The award ceiling is $386,575.

Who is eligible to apply?

Eligibility is limited to CESU partners under the Great Lakes Northern Forests CESU. The notice lists eligible applicants as "Others," with clarification in the full eligibility text, which generally means only organizations formally participating in that CESU consortium can apply.

When was the solicitation created and when was it originally due?

The solicitation was created on August 17, 2020, and the original closing date was August 28, 2020.

What is the broader outcome the funder is trying to achieve?

The broader outcome is to strengthen rapid detection capacity for emerging pathogens by benchmarking rapid pathogen identification and whole-genome assembly thresholds on accessible sequencing platforms, then converting those results into reproducible, transferable workflows and improved analytics that reduce guesswork for laboratories standing up sequencing-based diagnostics.

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