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Found 9 result(s)
The World Bank recognizes that transparency and accountability are essential to the development process and central to achieving the Bank’s mission to alleviate poverty. The Bank’s commitment to openness is also driven by a desire to foster public ownership, partnership and participation in development from a wide range of stakeholders. As a knowledge institution, the World Bank’s first step is to share its knowledge freely and openly.
Country
The National Microbial Data Center (NMDC) is jointly constructed by the Institute of Microbiology of the Chinese Academy of Sciences (IMS), the Institute of Oceanography of the Chinese Academy of Sciences, the Institute of Infectious Diseases of the Chinese Center for Disease Control and Prevention, the Institute of Plant Physiology and Ecology of the Chinese Academy of Sciences, and the Computer Network Information Centre of the Chinese Academy of Sciences. The General Office of the Chinese Academy of Sciences is the parent department. The data resources covering the whole life cycle of microbiological research, including microbiological resources, microbiological and cross-technological methods, research processes and engineering, microbiomics, microbiological technologies, as well as microbiological literature, patents, experts and results. The Centre focuses on promoting the convergence and integration of scientific and technological resources in the field of microbiology to the national platform, strengthening the development, application and analysis of microbiological resources, enhancing the effective use of microbiological resources and the ability to support scientific and technological innovation, and providing high-quality scientific and technological resource sharing services for scientific research, technological progress and social development.
Our knowledge of the many life-forms on Earth - of animals, plants, fungi, protists and bacteria - is scattered around the world in books, journals, databases, websites, specimen collections, and in the minds of people everywhere. Imagine what it would mean if this information could be gathered together and made available to everyone – anywhere – at a moment’s notice. This dream is becoming a reality through the Encyclopedia of Life.
Country
The National High Energy Physics Science Data Center (NHEPSDC) is a repository for high-energy physics. In 2019, it was designated as a scientific data center at the national level by the Ministry of Science and Technology of China (MOST). NHEPSDC is constructed and operated by the Institute of High Energy Physics (IHEP) of the Chinese Academy of Sciences (CAS). NHEPSDC consists of a main data center in Beijing, a branch center in Guangdong-Hong Kong-Macao Greater Bay Area, and a branch center in Huairou District of Beijing. The mission of NHEPSDC is to provide the services of data collection, archiving, long-term preservation, access and sharing, software tools, and data analysis. The services of NHEPSDC are mainly for high-energy physics and related scientific research activities. The data collected can be roughly divided into the following two categories: one is the raw data from large scientific facilities, and the other is data generated from general scientific and technological projects (usually supported by government funding), hereafter referred to as generic data. More than 70 people work in NHEPSDC now, with 18 in high-energy physics, 17 in computer science, 15 in software engineering, 20 in data management and some other operation engineers. NHEPSDC is equipped with a hierarchical storage system, high-performance computing power, high bandwidth domestic and international network links, and a professional service support system. In the past three years, the average data increment is about 10 PB per year. By integrating data resources with the IT environment, a state-of-art data process platform is provided to users for scientific research, the volume of data accessed every year is more than 400 PB with more than 10 million visits.
Country
The National Genomics Data Center (NGDC), part of the China National Center for Bioinformation (CNCB), advances life & health sciences by providing open access to a suite of resources, with the aim to translate big data into big discoveries and support worldwide activities in both academia and industry.
Country
China’s digital forestry information platform was constructed according to the criteria and index system of forest sustainable management. the relative social, economic, and politic data was considered and collected, the database represents not only the current forestry development, but also the social, politic, and economic situations.
Country
The National Population Health Data Center (NPHDC) is one of the 20 national science data center approved by the Ministry of Science and Technology and the Ministry of Finance. The Population Health Data Archive (PHDA) is developed by NPHDC relying on the Institute of Medical Information, Chinese Academy of Medical Sciences. PHDA mainly receives scientific data from science and technology projects supported by the national budget, and also collects data from other multiple sources such as medical and health institutions, research institutions and social individuals, which is oriented to the national big data strategy and the healthy China strategy. The data resources cover basic medicine, clinical medicine, public health, traditional Chinese medicine and pharmacy, pharmacy, population and reproduction. PHDA supports data collection, archiving, processing, storage, curation, verification, certification and release in the field of population health. Provide multiple types of data sharing and application services for different hierarchy users and help them find, access, interoperate and reuse the data in a safe and controlled environment. PHDA provides important support for promoting the open sharing of scientific data of population health and domestic and foreign cooperation.
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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.