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Found 7 result(s)

Addgene

Subject(s)
Content type(s)
Country
Addgene archives and distributes plasmids for researchers around the globe. They are working with thousands of laboratories to assemble a high-quality library of published plasmids for use in research and discovery. By linking plasmids with articles, scientists can always find data related to the materials they request.

Forschungsdatenzentrum am Robert Koch Institut

FDZ RKI

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Country
The Research Data Centre of the Robert Koch Institute (FDZ RKI) publishes the data of population-representative health surveys in the form of public use files (PUFs).The main purpose of health surveys is to generate a maximum amount of information on the state of health and health-related behaviour of Germany's resident population while ensuring an optimum use of funds. The methodology - i.e. the sample design, the principles on operationalization and measurement, and data-collection techniques - is largely modelled on the tried-and-tested methods of empirical social research. Health interview surveys (HIS) use established survey techniques such as filling out questionnaires, computer-assisted telephone interviews (CATI), computer-assisted personal interviews (CAPI), and online polling via the internet or email. The main difference compared to purely sociological surveys lies in the additional biomedical examinations, tests and medical-biochemical measurements, which generate significant added value in addition to the results of the surveys; this part is referred to internationally as the health examination survey (HES).

The Health Improvement Network

THIN

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THIN is a medical data collection scheme that collects anonymised patient data from its members through the healthcare software Vision. The UK Primary Care database contains longitudinal patient records for approximately 6% of the UK Population. The anonymised data collection, which goes back to 1994, is nationally representative of the UK population.

Avon Longitudinal Study of Parents and Children

ALSPAC

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Content type(s)
Country
ALSPAC is a longitudinal birth cohort study which enrolled pregnant women who were resident in one of three Bristol-based health districts in the former County of Avon with an expected delivery date between 1st April 1991 and 31st December 1992. Around 14,000 pregnant women were initially recruited. Detailed information has been collected on these women, their partners and subsequent children using self-completion questionnaires, data extraction from medical notes, linkage to routine information systems and from hands-on research clinics. Additional cohorts of participants have since been enrolled in their own right including fathers, siblings, children of the children and grandparents of the children. Ethical approval for the study was obtained from the ALSPAC Ethics and Law Committee (IRB00003312) and Local Research Ethics.

GESIS Suche

DBK

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Content type(s)
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<<<!!!<<< This record is no longer updated. Please use https://www.re3data.org/repository/r3d100012496 >>>!!!>>>

National Data Archive: An Online Microdata Library

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The National Data Archive has been disseminating microdata from surveys and censuses primarily under the Ministry of Statistics and Programme Implementation (MoSPI), Government of India. The archive is powered by the National Data Archive (NADA, ver. 4.3) software with DDI Metadata standard. It serves as a portal for researchers to browse, search, and download relevant datasets freely; even with related documentation (viz. survey methodology, sampling procedures, questionnaires, instructions, survey reports, classifications, code directories, etc). A few data files require the user to apply for approval to access with no charge. Currently, the archive holds more than 144 datasets of the National Sample Surveys (NSS), Annual Survey of Industries (ASI), and the Economic Census as available with the Ministry. However, efforts are being made to include metadata of surveys conducted by the State Governments and other government agencies.

LISS Panel

Longitudinal Internet Studies for the Social sciences

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Content type(s)
Country
The LISS panel (Longitudinal Internet Studies for the Social sciences) is the principal component of the MESS project. It consists of 5000 households, comprising approximately 7500 individuals. The panel is based on a true probability sample of households drawn from the population register by Statistics Netherlands. Households that could not otherwise participate are provided with a computer and Internet connection. In addition to the LISS panel an Immigrant panel was available from October 2010 up until December 2014. This Immigrant panel consisted of around 1,600 households (2,400 individuals) of which 1,100 households (1,700 individuals) were of non-Dutch origin. The data from this panel are still available through the LISS data archive (https://www.dataarchive.lissdata.nl/study_units/view/162). Panel members complete online questionnaires every month of about 15 to 30 minutes in total. They are paid for each completed questionnaire. One member in the household provides the household data and updates this information at regular time intervals.