DMP Guide: CONICET for Genomics & Bioinformatics
Learn how to design a fully compliant Data Management Plan (DMP) that satisfies Consejo Nacional de Investigaciones Científicas y Técnicas 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, Consejo Nacional de Investigaciones Científicas y Técnicas 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 open-access mandate from **Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)** expects PIs to index their **Genomics & Bioinformatics** findings in public repositories that support persistent citation IDs. Plans must be formulated and uploaded through the **SIGEVA** interface.
Verified Funder Open-Science Portfolio
Based on independent, open-science bibliometric data from OpenAlex, the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) oversees a massive scholarly ecosystem with over 81,057 published research outputs under their funding catalog, accumulating over 1,926,590 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 SIGEVA 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.
Computational pipelines in **Genomics & Bioinformatics** require raw sequence file storage alongside the exact containerized alignment code (Docker/Singularity) and statistical models to ensure full pipeline replication for **CONICET** audits.
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 CONICET 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
A compliant data management plan dmp for research projects in Genomics & Bioinformatics must detail the specific data collection methods and the precise data curation standards that govern the project. By configuring customizable dmptool workflows, research teams can seamlessly align their files with Consejo Nacional de Investigaciones Científicas y Técnicas's schemas. Our project methodology mandates systematic data cleaning and continuous verification of data integrity to support reproducible data wrangling pipelines. To aid secondary usage, a comprehensive data dictionary will accompany every published record. From a storage perspective, researchers must evaluate storing datasets in a highly indexed data warehouse versus a scalable data lake, analyzing the trade-offs of a data lake vs data warehouse architecture for downstream data analysis and exploratory data analysis inside the SIGEVA workspace. Open-access guidelines require teams to push finalised files to the dryad data repository, configure shared figshare datasets, or initiate a zenodo data upload, securing a permanent slot in the data citation index that aligns with nsf data management plan directives. We will enforce structured data versioning protocols using the open science framework osf to streamline reproducible data sharing that is fully compliant with fair data principles examples. Additionally, all collaborative research must respect the care data principles and uphold indigenous data sovereignty care policies, keeping community interest central to the data lifecycle. Implementing this storage layout satisfies compliance protocols overseen by the CONICET data audit team.
4. Frequently Asked Questions
Are we required to share all raw data from our research?
No, CONICET 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, CONICET 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.







