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Found 17 result(s)
Regionaal Archief Tilburg (RA Tilburg) is one of the four institutions of foundation Mommerskwartier and is based in Tilburg, the Netherlands. The statutory task (Public Records Act https://bit.ly/3iCTI7f) of RA Tilburg is to function as a repository for decentralized, local government organizations such as municipalities, communal schemes, and Water Authorities. RA Tilburg also manages private archives, and archives of organizations, institutes, or the public in general.
Country
Avibase is an extensive database information system about all birds of the world, containing over 60 million records about 10,000 species and 22,000 subspecies of birds, including distribution information, taxonomy, synonyms in several languages and more. This site is managed by Denis Lepage and hosted by Bird Studies Canada, the Canadian copartner of Birdlife International. Avibase has been a work in progress since 1992 and I am now pleased to offer it as a service to the bird-watching and scientific community.
The ESO/ST-ECF science archive is a joint collaboration of the European Organisation for Astronomical Research in the Southern Hemisphere (ESO) and the Space Telescope - European Coordinating Facility (ST-ECF). ESO observational data can be requested after the proprietary period by the astronomical community.
The Longitudinal Aging Study Amsterdam (LASA) at the VU University and VU University Medical Centre is initiated by the Ministry of Health, Welfare and Sports in 1991 to determine predictors and consequences of ageing. LASA focuses on, physical, emotional, cognitive and social functioning in late life, the connections between these aspects, and the changes that occur in the course of time
RETOPEA investigates the different ways in which religious coexistence is thought of in different environments and how religious peace treaties have been established in the past. The idea is to use the insights gained to inform thinking about present-day peaceful religious co-existence The dataset contains the contents and the metadata of the resources (i.e., clippings) published on the RETOPEA website (retopea.eu).
The Radiocarbon Palaeolithic Europe Database stores available radiometric data taken from literature and from other more restricted databases. Data is collected by continuous checking of newly published articles in hundreds of international and regional scientific journals and in collections or books dealing with a particular period or a specific Paleolithic site. User submissions are also accepted. Please note that this database is only available for download and local use via Microsoft Access or, in a more limited way, via Excel. As such, its accessibility is limited.
The Netherlands Cancer Registry is the national registration since 1989, providing statistics on cancer in the Netherlands. The registry is maintained by the Netherlands Comprehensive Cancer Organisation (IKNL). Data on incidence, prevalence, survival, mortality can be viewed in NCR data & figures on the IKNL website.
The Survey of Health, Ageing and Retirement in Europe (SHARE) is a multidisciplinary and cross-national panel database of micro data on health, socio-economic status and social and family networks of more than 140,000 individuals (approximately 530,000 interviews) aged 50 or over from 28 European countries and Israel.
Subject(s)
A domain-specific repository for the Life Sciences, covering the health, medical as well as the green life sciences. The repository services are primarily aimed at the Netherlands, but not exclusively.
Country
The Flanders Marine Institute (VLIZ) is a centre for marine and coastal research. As a partner in various projects and networks it promotes and supports the international image of Flemish marine scientific research and international marine education. In its capacity as a coordination and information platform, the Flanders Marine Institute (VLIZ) supports some thousand marine scientists in Flanders by disseminating their knowledge to policymakers, educators, the general public and scientists.
Content type(s)
Country
The Geodatenkatalog.de is the metadata information system of the Geodateninfrastruktur Deutschland (GDI-DE) and forms the data basis for Geoportal.de. With the help of this central component, metadata for geodata sets, geodata services, and other IT-supported geodata applications are collected and can be researched and retrieved via Geoportal.de.
The BHIC is an archive repository in 's-Hertogenbosch. It is the Regional Historical Centre (RHC) of the province of North Brabant and was created by a merger in 2005 of the former state archives and several regional archives in Northeast Brabant. It currently comprises nine municipalities, two water boards, the province of North Brabant and several joint arrangements (GRs). The BHIC has the legal task of managing (digital) archives in good, orderly and accessible condition for the above-mentioned decentralised authorities. In addition, the BHIC also manages private archives.
CLAPOP is the portal of the Dutch CLARIN community. It brings together all relevant resources that were created within the CLARIN NL project and that now are part of the CLARIN NL infrastructure or that were created by other projects but are essential for the functioning of the CLARIN (NL) infrastructure. CLARIN-NL has closely cooperated with CLARIN Flanders in a number of projects. The common results of this cooperation and the results of this cooperation created by CLARIN Flanders are included here as well.
Currently the institute has more than 700 collections consisting of (digital) research data, digitized material, archival collections, printed material, handwritten questionnaires, maps and pictures. The focus is on resources relevant for the study of function, meaning and coherence of cultural expressions and resources relevant for the structural, dialectological and sociolinguistic study of language variation within the Dutch language. An overview is here https://meertens.knaw.nl/en/datasets/
Content type(s)
The global scientific community, international partners, the private sector, civil society, and other relevant stakeholders establish a voluntary platform to link clinical trials registers in order to ensure a single point of access and the unambiguous identification of trials with a view to enhancing access to information by patients, families, patient groups and others.