Low-cost, High-Accuracy DNA Sequencing Technologies RFA, HG-97-002

National Human Genome Research Institute

National Institutes of Health
U.S. Department of Health and Human Services


Low-Cost, High-Accuracy DNA Sequencing Technologies

NIH GUIDE, Volume 26, Number 16, May 16, 1997
RFA: HG-97-002
P.T. 34
Letter of Intent Receipt Date: August 1, 1997
Application Receipt Date: October 16, 1997

National Human Genome Research Institute

PURPOSE

The purpose of this Request for Applications (RFA) is to stimulate research on next-generation technologies that have the potential to reduce the cost of high-accuracy genomic DNA sequencing by at least an order of magnitude.

HEALTHY PEOPLE 2000

The Public Health Service (PHS) is committed to achieving the health promotion and disease prevention objectives of "Healthy People 2000," a PHS-led national activity for setting priority areas. This RFA, Technologies for Genome Analysis, is related to the priority areas of cancer, heart disease and stroke, diabetes and chronic disability conditions, and maternal and infant health. Potential applicants may obtain a copy of "Healthy People 2000" (Full Report: Stock No. 017-001-00474-0 or Summary Report: Stock No. 017-001-00473-1) through the Superintendent of Documents, Government Printing Office, Washington, DC 20402-9325 (telephone 202-512-1800).

ELIGIBILITY REQUIREMENTS

Applications may be submitted by domestic for-profit and non-profit organizations, public and private, such as universities, colleges, hospitals, laboratories, companies, units of State and local governments, and eligible agencies of the Federal government. Racial/ethnic minority individuals, women, and persons with disabilities are encouraged to apply as Principal Investigators. Applications from foreign institutions will not be accepted. However, subcontracts to foreign institutions are allowable, with sufficient justification.

MECHANISM OF SUPPORT

This RFA will use the National Institutes of Health (NIH) research project grant (R01), First Independent Research Support and Transition (FIRST) (R29) award, exploratory/developmental grant (R21), and program project (P01) mechanisms. The total project period for an R01 or P01 application submitted in response to this RFA may not exceed three years. R29 grants are subject to the usual conditions for the FIRST awards. Exploratory/developmental (R21) grants will be limited to $100,000 direct cost per year for a maximum of 3 years (one year longer than NHGRI's standard R21 grant). The R21 grant mechanism is used to support highly creative approaches for which substantial preliminary data are not yet available. The R21 grants are not renewable, but future project continuation is possible through other grant mechanisms such as the R01 or P01. Responsibility for the planning, direction, and execution of the proposed project will be solely that of the applicant. Awards will be administered under PHS grants policy as stated in the Public Health Service Grants Policy Statement. The anticipated award date is July 1, 1998. It is anticipated that another RFA related to DNA sequencing technology will be issued by NHGRI next year.

FUNDS AVAILABLE

It is anticipated that approximately $5 million (total costs) will be available for this initiative in Fiscal Year 1998. NHGRI anticipates that projects at very different stages of development will be submitted in response to this RFA. Therefore, the size of awards may vary substantially; accordingly the number of grants funded may be as few as five or as many as 20, depending on the quality and scope of the applications received. Awards pursuant to this RFA are contingent upon the availability of funds for this purpose. The amount of funding for this solicitation may be increased if a large number of highly meritorious applications is received and if funds are available. Only applications found to be of high scientific merit will be considered for funding and all of the funds will not be spent if there are not enough highly meritorious applications. Any applicant planning to submit an application for more than $500,000 direct cost in any one year MUST contact the NHGRI staff listed under INQUIRIES in order for the application to be accepted by NIH.

RESEARCH OBJECTIVES

Background

NHGRI is currently engaged, along with several other federal, private, and international organizations, in a fifteen year research program called the Human Genome Project (HGP). The goals are to characterize the genomes of human and selected model organisms, to develop technologies to analyze the human genome, to examine the ethical, legal, and social implications of human genetics research, and to train scientists who will be able to utilize the tools and resources developed through the HGP to pursue biological studies that will improve human health.

Significant progress toward completing these goals has been made in the past seven years, with several having already been achieved. The genetic mapping goals for both the human and the mouse have been met. Progress toward the human and mouse physical mapping goals is steady, with sufficient support in place to allow the achievement of these goals ahead of schedule. There has also been good progress toward meeting the sequencing goals. The genomic sequence of both E. coli and S. cerevisiae have been determined, the sequence of C. elegans is expected to be finished by 1998, and the complete sequence of D. melanogaster is expected to be finished shortly after the end of this century.

As a result of recent improvements in sequencing technology and strategies, confidence is high that current technology, enhanced by foreseeable improvements, will be sufficient to complete a reference human genomic DNA sequence by the target date, 2005. To this end, pilot projects for large-scale production of human genomic DNA sequence were initiated in 1996. However, even with anticipated improvements, DNA sequencing is likely to remain too expensive to meet the scientific demand for sequence information. For example, additional sequencing will be needed to understand the sequence variation between individuals that is associated with individual differences in inherited susceptibility to disease. Such studies may require obtaining the sequence of much of the genomic DNA from large numbers (tens to possibly thousands) of individuals. Similarly, the utility of the initial complete genomic sequence of a few organisms for understanding their biology will increase the incentive to collect genomic sequence information for many other organisms to study their biology and evolutionary and symbiotic relationships. DNA sequencing of that magnitude can only be contemplated when sequencing techniques have been made considerably more cost-effective and robust than they are today, or will be in the foreseeable future. The purpose of this RFA is to stimulate the development of the technologies needed to achieve these goals.

Objectives and Scope

Technologies for de novo sequencing and re-sequencing are needed. It should be noted that the conceptual distinction between these DNA sequencing technologies is not fundamental, but is instead a function of the limitations of the technologies as currently implemented. As novel methods are introduced and sequencing technologies mature, throughput and accuracy will increase and cost will decrease, and the distinction may not persist. However, at least for the present, the capabilities of these approaches and their potential near-term applications are sufficiently different to justify distinguishing between them for the purpose of this RFA.

De novo sequencing involves determining DNA sequence without any prior knowledge of that sequence. The initial reference human sequence will be determined by de novo sequencing, as were the sequences of yeast, H. influenzae, M. genitalium, M. jannaschii, and E. coli. Technology for de novo sequencing will continue to be needed to determine the complete sequence of the genomes of numerous other organisms including pathogens, agriculturally important organisms, and those that have utility as model organisms and sources of pharmaceutical products.

Technology is also needed for re-sequencing or rapidly comparing sequences to identify differences. Re-sequencing takes advantage of sequence information obtained from one sample, to design a more efficient approach to determining the sequence of another, similar sample. Today's re-sequencing technologies are effective for samples that are extremely similar (e.g., for identifying single-base differences in a particular gene isolated from two individuals). With additional development, however, the data quality and throughput of re-sequencing technology may be improved, and expanded to allow determination of sequence in cases such as insertions or deletions relative to a reference sequence. Re-sequencing technology may be the most cost-effective way, for example, to collect the large amounts of sequence data from large numbers of individuals that is needed to understand the sequence variations associated with individual differences in inherited susceptibility to disease.

This RFA seeks to stimulate research on next-generation technologies (including those for de novo sequencing, re-sequencing, or both) that have the potential to reduce the cost of high-accuracy genomic DNA sequencing by at least an order of magnitude. State-of-the-art technology can currently generate de novo sequence data containing less than 1 error per 10,000 base pairs at a total cost (including machines, personnel, supplies, and overhead) of approximately $0.50 per base pair. The goal of research under this RFA will be to drive the total cost of obtaining accurate (<1 error in 10,000 bp) de novo sequence to well below $0.05 per base pair; re-sequencing should cost considerably less.

Applications responsive to this RFA will include those designed to:

Applicants should directly address the advantages of the proposed approach over existing approaches, and justify their assertion that successful development of the technology will result in a ten-fold decrease in the cost of sequencing. Applicants proposing to develop technologies for which proof of principle for DNA sequencing has not yet been demonstrated should describe clearly the manner in which the proposed technology might be applied to sequencing. For such projects, it will be difficult to predict with confidence the cost of sequencing using the technology. It is therefore particularly important to present a clear conceptual overview of the entire system in which the technology would be used and if possible to estimate the cost of developing, producing, and using such a system.

Current DNA sequencing approaches require some combination of steps, including the isolation of DNA from biological samples, biochemical amplification of the DNA within the sample, incorporation of fluorescent label into the sample, determination of the nucleotide sequence of each sample, "assembly" of data from numerous overlapping and redundant determinations into a continuous dataset, and analysis of the sequence data. As new technologies are developed, some or all of these steps may still be required. Research on all of these steps, and particularly on the integration of steps into a continuous process, will be supported under this RFA. For projects whose aim is to develop integrated systems, applicants should address the throughput of the various system components, and how the entire system will support the achievement of the cost and quality goals of this RFA.

The RFA will also accept applications to develop computational tools needed in support of systems or in conjunction with components eligible for funding under this RFA. Support for development of computational tools may be included as part of the technology development application. An application to develop computational tools that is submitted independently of a proposal to develop hardware systems should describe how the results of the independent research will be integrated with existing or planned technology.

The following types of research will NOT be supported under this RFA: projects to improve slab gels, microchannels, and capillary array electrophoresis, in systems in which the well-to-read distance is measured in tens of centimeters. This type of research is currently receiving support from NHGRI as a result of recent RFAs. However, NHGRI continues to encourage this type of technology development for DNA sequencing; applications for such studies should be submitted under the Program Announcement PA-97-044, Technologies for Genomic Mapping, Sequencing, and Analysis.

INCLUSION OF WOMEN AND MINORITIES IN RESEARCH INVOLVING HUMAN SUBJECTS

It is the policy of the NIH that women and members of minority groups and their sub-populations must be included in all NIH supported biomedical and behavioral research projects involving human subjects, unless a clear and compelling rationale and justification is provided that inclusion is inappropriate with respect to the health of the subjects or the purpose of the research. This policy results from the NIH Revitalization ACT of 1993 (Section 492B of Public Law 103- 43).

All investigators proposing research involving human subjects should read the "NIH Guidelines for Inclusion of Women and Minorities as Subjects in Clinical Research," which have been published in the Federal Register of March 28, 1994 (FR 59 14508-14513) and in the NIH Guide for Grants and Contracts, Volume 23, Number 11, March 18, 1994.

Special Requirements

Statement of milestones: It has been the experience of NGHRI that technology development projects that establish a clear statement of their milestones, and benchmarks by which attainment of those milestones can be measured, make more rapid progress toward achieving their short- and long-range goals. Therefore, applicants should present a clear timetable for the achievement of specific milestones, and should define the benchmarks by which progress toward those milestones will be measured. Both the milestones and benchmarks should be stated as quantitatively as possible.

Dissemination of the results of technology development research: Proposals should address the issue of access by groups other than the developers to any instruments or software developed through this program.

Post-award management: During the course of the grant period, technologies will improve and the rate of progress and focus of work supported by the grants may change. It is expected that the principal investigators will make any necessary adjustments in scientific direction to accommodate the changing environment. During the award period, the principal investigators may be invited to meet with NIH program staff in Bethesda, MD, or at the grantee site, to review scientific progress. Other scientists external to and knowledgeable about these studies may also be invited to participate. Applicants should include travel funds for the P.I. to meet annually with NIH staff in the Washington D.C. area, should such meetings be advisable.

Special human subjects issues: Recently, it has become evident that special human subjects issues are raised by the large-scale sequencing of human genomic DNA because large amounts of DNA sequence information from single individuals may be generated. Similar issues can be anticipated in projects in which sequence variations are identified in individuals. The NHGRI and the DOE have recently issued a document, "Guidance on Human Subjects Issues in Large-Scale DNA Sequencing". Any application submitted in response to this RFA that includes a plan to sequence at least 1 megabase of human DNA during the period of the grant, or to determine a large number of human sequence polymorphisms, in the context of testing the technology under development, should address these special human subjects issues.

LETTER OF INTENT

Prospective applicants are asked to submit, by August 1, 1997, a letter of intent that includes a descriptive title of the proposed research, the name, address, and telephone number of the Principal Investigator, and the identities of other key personnel and participating institutions, and the number and title of the RFA in response to which the application may be submitted. Although a letter of intent is not required, is not binding, and does not enter into the review of a subsequent application, it can help establish an early dialogue with NHGRI staff, and the information that it contains allows NHGRI staff to estimate the potential review workload and to avoid conflict of interest in the review.

The letter of intent is to be sent to:

Jeffery A. Schloss Ph.D.
Division of Extramural Research
National Human Genome Research Institute
Building 38A, Room 614
Bethesda, MD 20892-6050
Phone: (301) 496-7531
Fax: (301) 480-2770
E-mail Jeffery A. Schloss

APPLICATION PROCEDURES

The research grant application form PHS 398 (rev. 5/95) is to be used in applying for these grants. These forms are available at most institutional offices of sponsored research; from the Division of Extramural Outreach and Information Resources, National Institutes of Health, 6701 Rockledge Drive, MSC 7910, Bethesda, MD 20892-7910, telephone 301/435-0714, e-mail: ASKNIH@odrockm1.od.nih.gov; and from the program administrator listed under INQUIRIES.

The RFA label available in the application form must be affixed to the bottom of the face page of the application. Failure to use this label could result in delayed processing of the application such that it may not reach the review committee in time for review. In addition, the RFA title and number must be typed on line 2 of the face page of the application form and the YES box must be marked.

Submit a signed, typewritten original of the application, including the Checklist, and three signed photocopies, in one package to:

Division of Research Grants
National Institutes of Health
6701 Rockledge Drive, Room 1040
Bethesda, MD 20892-7710
Bethesda, MD 20817 (for express/courier service)

At the time of submission, two additional copies of the application, including appendices, must also be sent to:

Rudy Pozzatti, Ph.D.
Office of Scientific Review
National Human Genome Research Institute
Building 38A, Room 613
Bethesda, MD 20892-6050

Applications must be received by October 16, 1997. If an application is received after that date, it will be returned to the applicant without review. The Division of Research Grants (DRG) will not accept any application in response to this RFA that is essentially the same as one currently pending initial review, unless the applicant withdraws the pending application. The DRG will not accept any application that is essentially the same as one already reviewed. This does not preclude the submission of substantial revisions of applications already reviewed, but such applications must include an introduction addressing the previous critique. The applicants should also ensure that their revised applications respond to the review criteria by which applications received in response to this RFA will be evaluated.

REVIEW CONSIDERATIONS

Upon receipt, applications will be reviewed for completeness by DRG and for responsiveness to the RFA by NHGRI program staff. Incomplete applications will be returned to the applicant without further consideration. If the application is not responsive to the RFA, NIH staff will contact the applicant to determine whether to return the application to the applicant or submit it for review in competition with unsolicited applications at the next review cycle.

Those applications that are complete and responsive will be evaluated for scientific and technical merit in accordance with the criteria stated below by an appropriate peer review group convened by the NHGRI. As part of the initial merit review, all applications will receive a written critique and may undergo a process in which only those applications deemed to have the highest scientific merit will be discussed and assigned a priority score. All applications will receive a second level of review by the National Advisory Council for Human Genome Research.

Review Criteria

For R21 applications, preliminary data are not required. However, the applicant does have the responsibility for developing a sound research plan and for presenting any other information that can be considered as evidence of feasibility.

AWARD CRITERIA

Factors that will be used to make award decisions are:

INQUIRIES

Inquiries concerning this RFA are encouraged. The opportunity to clarify any issues or questions from potential applicants is welcome.

Direct inquiries regarding programmatic issues to:

Jeffery A. Schloss Ph.D.
Division of Extramural Research
National Human Genome Research Institute
Building 38A, Room 614
Bethesda, MD 20892-6050
Phone: (301) 496-7531
Fax: (301) 480-2770
E-mail Jeffery A. Schloss

Direct inquiries regarding fiscal matters to:

Ms. Jean Cahill
Grants Management Office
National Human Genome Research Institute
Building 38A, Room 613, MSC 6050
Bethesda, MD 20892-6050
Phone: (301) 402-0733
Fax: (301) 402-1951
E-mail:Ms. Jean Cahill

AUTHORITY AND REGULATIONS

This program is described in the Catalog of Federal Domestic Assistance No. 93.172. Awards are made under authorization of the Public Health Service Act, Title IV, Part A (Public Law 78-410, as amended by Public Law 99-158, 42 USC 241 and 285) and administered under PHS grants policies and Federal Regulations 42 CFR 52 and 45 CFR Part 74. This program is not subject to the intergovernmental review requirements of Executive Order 12372 or Health Systems Agency review.

The PHS strongly encourages all grant recipients to provide a smoke-free workplace and promote the non-use of all tobacco products. In addition, Public Law 103-227, the Pro-Children Act of 1994, prohibits smoking in certain facilities (or in some cases, any portion of a facility) in which regular or routine education, library, day care, health care or early childhood development services are provided to children. This is consistent with the PHS mission to protect and advance the physical and mental health of the American people.

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Last Reviewed: February 23, 2012