Filter
Reset all

Subjects

Content Types

Countries

AID systems

API

Data access

Data access restrictions

Database access

Database access restrictions

Database licenses

Data licenses

Data upload

Data upload restrictions

Enhanced publication

Institution responsibility type

Institution type

Keywords

Metadata standards

PID systems

Provider types

Quality management

Repository languages

Software

Repository types

Versioning

  • * at the end of a keyword allows wildcard searches
  • " quotes can be used for searching phrases
  • + represents an AND search (default)
  • | represents an OR search
  • - represents a NOT operation
  • ( and ) implies priority
  • ~N after a word specifies the desired edit distance (fuzziness)
  • ~N after a phrase specifies the desired slop amount
  • 1 (current)
Found 12 result(s)
Repository type(s)
  • other
Provider type(s)
  • dataProvider
Country
The Alcohol and Gaming Commission of Ontario’s Data Inventory lists all of the agency’s data sets and identifies whether a data set is currently open, in the process of being opened or exempt from being released as open data due to legal, security, privacy, confidentiality or commercially-sensitive reasons.
Repository type(s)
  • institutional
Provider type(s)
  • serviceProvider
  • dataProvider
The N3C Data Enclave is a secure portal containing a very large and extensive set of harmonized COVID-19 clinical electronic health record (EHR) data. The data can be accessed through a secure cloud Enclave hosted by NCATS and cannot be downloaded due to regulatory control. Broad access is available to investigators at institutions that sign a Data Use Agreements and via Data Use Requests by investigators. The N3C is a unique open, reproducible, transparent, collaborative team science initiative to leverage sensitive clinical data to expedite COVID-19 discoveries and improve health outcomes.
Repository type(s)
  • institutional
Provider type(s)
  • dataProvider
Country
REDU is the institutional open research data repository of the University of Campinas, Brazil. It contains research data produced by all research groups of the University, in a wide range of scientific domains, which are indexed by DataCite DOI. Created at the end of 2020, it is coordinated by a scientific and technical committee composed by data librarians, IT professionals, and scientists representing user groups. Implemented on top of Dataverse, it exports metadata using OAIS. Files with sensitive content (due to ethics or legal constraints) are not stored therein - rather, only their metadata is recorded in REDU, as well as contact information so that interested researchers can contact the persons responsible for the files for conditional subsequent access. It is being little by little populated, following the University's Open Science policies.
Repository type(s)
  • institutional
Provider type(s)
  • dataProvider
  • serviceProvider
LSHTM Data Compass is a curated digital repository of research outputs that have been produced by staff and students at the London School of Hygiene & Tropical Medicine and their collaborators. It is used to share outputs intended for reuse, including: qualitative and quantitative data, software code and scripts, search strategies, and data collection tools.
Repository type(s)
  • disciplinary
Provider type(s)
  • serviceProvider
  • dataProvider
Country
SAGE is a data and research platform that enables the secondary use of data related to child and youth development, health and well-being. It currently contains research data, and at a later stage we aim to also house administrative and community service delivery data. Technical infrastructure and governance processes are in place to ensure ethical use and the privacy of participants. This dataverse provides metadata for the various data holdings available in SAGE (Secondary Analysis to Generate Evidence), a research data repository based in Edmonton Alberta and an intiative of PolicyWise for Children & Families. In general, SAGE contains data holdings too sensitive for open access. Each study lists a security level which indicates the procedure required to access the data.
Repository type(s)
  • institutional
Provider type(s)
  • dataProvider
Yoda is a data repository built by Utrecht University and hosted by SURF for the Vrije Universiteit Amsterdam. Yoda can store and share all kinds of scientific research data in a safe way (encrypted, stored in multiple geo locations). Yoda takes care of publishing research data with its metadata as datasets and making them findable for different harvesters. Yoda, short for Your data, is an integrated digital environment to support all kind of researchers from different backgrounds during and after their research. Yoda is based on open source software iRODS. During the development of the key features the most important aim was to make daily life of researchers more easy as far as data management and the requirements of funders are concerned. Yoda publishes data packages via DataCite. Datacite Commons can be used to find data packages: https://commons.datacite.org/doi.org?query=client.uid:delft.vudata
Repository type(s)
  • disciplinary
Provider type(s)
  • dataProvider
Country
The Canadian VirusSeq Data Portal (CVDP) is an open-access data portal funded by Genome Canada. It is intended to facilitate access to Canadian SARS-CoV-2 sequences and associated non-sensitive metadata adhering to the FAIR Data principles. Limited contextual metadata and viral genome sequences can be shared among Canadian public health labs, researchers and other groups interested in accessing the data for surveillance, research, and innovation purposes. The CVDP will harmonize, validate, and automate submission to international databases and enable the creation of real-time dashboards that summarize the Canadian data contributions while facilitating exploration and access. Sequences or metadata submitted to the CVDP may not include data that could reveal the personal identity of the source. Its is part of Canadian COVID Genomics Network (CanCOGeN).
Repository type(s)
  • disciplinary
Provider type(s)
  • serviceProvider
The MDR harvests metadata on data objects from a variety of sources within clinical research (e.g. trial registries, data repositories) and brings that together in a single searchable portal. The metadata is concerned with discoverability, access and provenance of the data objects (which because the data may be sensitive will often be available under a controlled access regime). At the moment (01/2021) the MDR obtains study data from: Clinical Trials.gov (CTG), The European Clinical Trials Registry (EUCTR), ISRCTN, The WHO ICTRP
Repository type(s)
  • disciplinary
Provider type(s)
  • dataProvider
  • serviceProvider
The Virtual Research Environment (VRE) is an open-source data management platform that enables medical researchers to store, process and share data in compliance with the European Union (EU) General Data Protection Regulation (GDPR). The VRE addresses the present lack of digital research data infrastructures fulfilling the need for (a) data protection for sensitive data, (b) capability to process complex data such as radiologic imaging, (c) flexibility for creating own processing workflows, (d) access to high performance computing. The platform promotes FAIR data principles and reduces barriers to biomedical research and innovation. The VRE offers a web portal with graphical and command-line interfaces, segregated data zones and organizational measures for lawful data onboarding, isolated computing environments where large teams can collaboratively process sensitive data privately, analytics workbench tools for processing, analyzing, and visualizing large datasets, automated ingestion of hospital data sources, project-specific data warehouses for structured storage and retrieval, graph databases to capture and query ontology-based metadata, provenance tracking, version control, and support for automated data extraction and indexing. The VRE is based on a modular and extendable state-of-the art cloud computing framework, a RESTful API, open developer meetings, hackathons, and comprehensive documentation for users, developers, and administrators. The VRE with its concerted technical and organizational measures can be adopted by other research communities and thus facilitates the development of a co-evolving interoperable platform ecosystem with an active research community.
Repository type(s)
  • disciplinary
Provider type(s)
  • dataProvider
HI HOPES aims is to provide free home based support and information without bias to every family with an infant or toddler with hearing loss. Through an early intervention framework of care, support, information and partnership in a culturally sensitive, community based manner to allow we aim to empower the family in their home environment and help the baby with a hearing loss to reach her/his full potential.
Repository type(s)
  • disciplinary
Provider type(s)
  • serviceProvider
Country
Birdata is your gateway to BirdLife Australia data including the Atlas of Australian Birds and Nest record scheme. You can use Birdata to draw bird distribution maps and generate bird lists for any part of the country. You can also join in the Atlas and submit survey information to this important environmental database. Birdata is a partnership between Birds Australia and the Tony and Lisette Lewis Foundation's WildlifeLink program to collect and make Birds Australia data available online.