DMP Guide: NRF for Genomics & Bioinformatics
Learn how to design a fully compliant Data Management Plan (DMP) that satisfies National Research Foundation open-data policies. Explore optimal file formats, metadata mapping, and repository selection for Genomics & Bioinformatics research data.
1. Funder Policy & Open Data Compliance
In alignment with international open-science mandates, National Research Foundation requires all principal investigators to submit a comprehensive Data Management Plan (DMP) with their grant application. A robust DMP details how research data will be collected, processed, documented, stored, shared, and preserved both during and after the project.
Funder-Specific Mandate Directive
The **National Research Foundation (NRF)** open-science policy expects research data in **Genomics & Bioinformatics** to be managed, documented, and archived in public repositories supporting persistent identifiers. Plans must be submitted through the **NRF Portal** portal.
Verified Funder Open-Science Portfolio
Based on independent, open-science bibliometric data from OpenAlex, the National Research Foundation (NRF) oversees a massive scholarly ecosystem with over 271,610 published research outputs under their funding catalog, accumulating over 7,129,508 citations across the global scientific record. To protect the public's investment in this massive knowledge corpus, the funder strictly enforces FAIR data management and open repository deposits, making compliance with this DMP protocol mandatory for all awarded grants.
For projects in the field of Genomics & Bioinformatics, managing data correctly is essential not only for compliance, but also to support peer-review validation and reproducibility. All DMPs must be submitted through the NRF Portal portal, using standard institutional guidelines.
2. Data Types, Formats, and Metadata Standards
A high-quality DMP must explicitly identify the types of data that will be generated and specify open, non-proprietary file formats to ensure long-term usability. For Genomics & Bioinformatics, datasets typically range from raw observational measurements to curated computational models.
In the domain of computational **Genomics & Bioinformatics**, investigators must archive both the raw input datasets and the containerized software (Docker/Singularity) used for analysis. This ensures that **NRF** compliance officers can verify and replicate pipeline executions.
To guarantee discoverability, datasets should be documented using standardised metadata schemas that map to the Genetic Phenomena branch of scholarly vocabularies. This ensures indexers and crawlers can crawl and identify research outputs accurately.
| DMP Component | Custom Target Value for Genomics & Bioinformatics |
|---|---|
| Preferred File Formats | FASTA/FASTQ (raw sequencing), BAM/SAM (alignments), VCF (variant calls), HDF5 (genomic coordinates) |
| Metadata Schema Standard | MINSEQE standards, SRA XML metadata, CodeMeta schema |
| Target Scientific Repositories | NCBI Sequence Read Archive (SRA), ENA, Zenodo, and directory servers mapped in PubMed, NCBI & European Nucleotide Archive |
3. Step-by-Step DMP Construction Protocol
When preparing your DMP for a NRF proposal, structure your document around these core sections:
- Data Collection and Generation:
Describe the methodology, instrumentation, or software used to collect or generate new data. Detail quality assurance and quality control measures implemented at your facility. - Documentation and Metadata:
Explain how the data will be documented, including accompanying read-me files, data dictionaries, and laboratory notebooks. Specify the metadata standards to be utilized (using MINSEQE standards, SRA XML metadata, CodeMeta schema as standard). - Ethics, Intellectual Property, and Consent:
Address how sensitive or confidential datasets will be handled. Detail anonymisation processes, access controls, and compliance with institutional ethics boards. - Storage, Backups, and Security:
State where data will be stored during active research. Detail automated backup schedules, server redundancies, and access authorisation protocols. - Long-Term Preservation and Archiving:
Select the digital repository for post-project archiving (such as NCBI Sequence Read Archive (SRA), ENA, Zenodo, and directory servers mapped in PubMed, NCBI & European Nucleotide Archive). Confirm that the repository supports persistent identifiers (handles/DOIs) and provides secure preservation.
Open Science Workflows, Data Curation & Repositories
Establishing a robust data management plan dmp for Genomics & Bioinformatics requires outlining rigorous data collection methods alongside established data curation standards from day one. PIs can leverage structured dmptool workflows to coordinate these data frameworks for review by National Research Foundation. Adhering to NRF requirements means detailing how raw files undergo data cleaning, how researchers verify ongoing data integrity, and which tools handle automated data wrangling. Additionally, a standardized data dictionary must be compiled to guarantee metadata clarity. For active storage, the proposal compares a relational data warehouse schema against an unstructured data lake model, reviewing the functional benefits of a data lake vs data warehouse environment for general data analysis and initial exploratory data analysis of study outputs. To ensure permanent access, datasets will be deposited in the dryad data repository, hosted as figshare datasets, or archived via a secure zenodo data upload, enabling inclusion in the data citation index and fulfilling standard nsf data management plan and local NRF requirements. To support replication, we will establish strict data versioning protocols on the open science framework osf to guide reproducible data sharing that follows fair data principles examples. When working with sensitive community records, the project will strictly observe the care data principles and indigenous data sovereignty care guidelines to guarantee ethical data stewardship in accordance with NRF rules. Aligning the archiving schedule directly with NRF open-access metrics protects the project's funding cycles.
4. Frequently Asked Questions
Are we required to share all raw data from our research?
No, NRF policies generally recognise that some data cannot be shared publicly due to privacy, security, intellectual property, or commercialisation constraints. In such cases, your DMP must justify why certain datasets are restricted and describe how metadata will still be made discoverable.
Who owns the research data generated under this grant?
Data ownership is typically held by the host institution, subject to co-ownership clauses in collaborative projects. However, NRF guidelines require that data be made as openly available as possible under open licensing, such as Creative Commons or Open Data Commons.
DMP Specifications
FAIR Principles
Your plan must align with the FAIR Principles:
- Findable: Rich metadata and persistent DOIs.
- Accessible: Free retrieval via standard protocols.
- Interoperable: Open formats and vocabulary alignment (such as MINSEQE standards, SRA XML metadata, CodeMeta schema).
- Reusable: Clear data licensing and reuse guidelines.







