List of required information for application:
1. Project Title: A clear and concise title for the research project.
2. Project Summary: A brief summary of the proposed research, including the objectives, methods, and expected outcomes.
3. Project Description: A detailed description of the research project, including the research questions, methodology, data collection and analysis methods, and potential implications.
4. Significance and Innovation: An explanation of the significance and innovation of the proposed research, highlighting its potential impact on the field.
5. Research Plan: A detailed plan outlining the specific aims, hypotheses, and experimental design of the research project.
6. ELSI Focus: A clear explanation of how the proposed research will specifically address the ethical, legal, and social implications of human genome research.
7. Methodology: A description of the research methodology and approach, including any data-generating qualitative and quantitative methods, legal and normative analyses, or other research methodologies.
8. Stakeholder Engagement: If applicable, an explanation of how stakeholders will be directly engaged in the research project.
9. Timeline: A detailed timeline for the proposed research activities, including milestones and deliverables.
10. Budget: A comprehensive budget breakdown, including personnel costs, equipment, supplies, travel, and any other direct costs associated with the research project.
11. References: A list of relevant references and sources cited in the application.
12. Biographical Sketches: Biographical sketches of the principal investigator and other key personnel involved in the research project.
13. Facilities and Resources: A description of the facilities, equipment, and resources available to support the proposed research.
14. Data Management: A plan for data management, including data collection, storage, sharing, and preservation.
15. Human Subjects and Ethics: A description of how human subjects will be involved in the research project, including any ethical considerations and plans for obtaining informed consent.
16. Regulatory Approvals: Documentation of any required regulatory approvals, such as Institutional Review Board (IRB) approval.
17. Collaboration and Partnerships: If applicable, information on any collaborations or partnerships with other institutions or organizations.
18. Potential Impact: An explanation of the potential impact and relevance of the proposed research to the field of human genome research and its broader implications.
