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Found 72 result(s)
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An Open Science resource that promotes scientific research and discovery in neurological diseases and accelerates the development of new treatments. It includes a growing collection of biospecimens, longitudinal clinical and neuropsychiatric information, imaging and genetic data from patients with neurological disease as well as healthy controls.
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Welcome to the District of North Vancouver’s Open Data portal. Here you have access to many free datasets which you can use in your printed products or online services – completely free of charge. Our datasets are updated automatically and refreshed each week. Every dataset comes with its own metadata providing valuable information on the origin, history, accuracy and completeness of the dataset.
A curated database of mutations and polymorphisms associated with Lafora Progressive Myoclonus Epilepsy. The Lafora progressive myoclonus epilepsy mutation and polymorphism database is a collection of hand curated mutation and polymorphism data for the EPM2A and EPM2B (NHLRC1) from publicly available literature: databases and unpublished data. The database is continuously updated with information from in-house experimental data as well as data from published research studies.
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The Global Proteome Machine (GPM) is a protein identification database. This data repository allows users to post and compare results. GPM's data is provided by contributors like The Informatics Factory, University of Michigan, and Pacific Northwestern National Laboratories. The GPM searchable databases are: GPMDB, pSYT, SNAP, MRM, PEPTIDE and HOT.
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The Environment Canada Data Catalogue provides a one-stop solution to describing, publishing and discovering EC's environmental and scientific data.
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The City of Burnaby maintains a wide range of data. As part of our commitment to engagement, transparency and accountability, we want to share our data with you. Please explore this site and use Burnaby’s data to analyze information, build apps, combine open datasets using maps, develop new web and mobile applications, and to meet your specific data needs. Together, using open data, we’ll make our great community even better!
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Data can help you identify problems, perform forecasting, monitor change, set priorities, manage and respond to events and understand trends. Our City of Abbotsford Data Hub is the platform for exploring and downloading data, discovering and building apps, and engaging others to solve important issues. You can analyze and combine datasets using maps, as well as develop new web and mobile applications. The city is committed to supporting community engagement, enhancing transparency and accountability to our residents by providing public access to our data. Let's work together to achieve our goals!
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This is the City of Fredericton’s public platform for exploring and downloading open data, discovering and building apps, and engaging in solutions important to local issues. Our site is built on the Esri™ Open Data portal platform. The site in includes various data sets and over 20 apps.
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This City of London open data platform serves to be a one stop shop for information for residents, students, non-profits and businesses throughout the city. Anyone can use open data from the City of London at no cost. Download raw data and share your insights with the rest of your community or build new applications that serve specific users.
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The Region of Peel Data Portal provides a central place to access data about Peel Region. We have information on topics such as demographics, population, housing, economic activity, and the operations of the Region.
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A free and open data-sharing portal providing access to the definitive source of geographic and other data relating to the City of Markham.
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Welcome to Conservation Halton's platform for exploring and downloading open data, discovering web maps, and engaging communities to solve important local issues
The objective of the Database of Genomic Variants is to provide a comprehensive summary of structural variation in the human genome. We define structural variation as genomic alterations that involve segments of DNA that are larger than >1kb. Now we also annotate InDels in 100bp-1kb range. The content of the database is only representing structural variation identified in healthy control samples. The Database of Genomic Variants provides a useful catalog of control data for studies aiming to correlate genomic variation with phenotypic data. The database is continuously updated with new data from peer reviewed research studies. We always welcome suggestions and comments regarding the database from the research community.
The THEMIS mission is a five-satellite Explorer mission whose primary objective is to understand the onset and macroscale evolution of magnetospheric substorms. The five small satellites were launched together on a Delta II rocket and they carry identical sets of instruments including an electric field instrument (EFI), a flux gate magnetometer (FGM), a search coil magnetometer (SCM), a electro-static analyzer, and solid state telescopes (SST). The mission consists of several phases. In the first phase, the spacecraft will all orbit as a tight cluster in the same orbital plane with apogee at 15.4 Earth radii (RE). In the second phase, also called the Dawn Phase, the satellites will be placed in their orbits and during this time their apogees will be on the dawn side of the magnetosphere. During the third phase (also known as the Tail Science Phase) the apogees will be in the magnetotail. The fourth phase is called the Dusk Phase or Radiation Belt Science Phase, with all apogees on the dusk side. In the fifth and final phase, the apogees will shift to the sunward side (Dayside Science Phase). The satellite data will be combined with observations of the aurora from a network of 20 ground observatories across the North American continent. The THEMIS-B (THEMIS-P1) and THEMIS-C (THEMIS-P2) were repurposed to study the lunar environment in 2009. The spacecraft were renamed ARTEMIS (Acceleration, Reconnection, Turbulence and Electrodynamics of the Moon’s Interaction with the Sun), with the P1 and P2 designations maintained.
Pathway Commons is a convenient point of access to biological pathway information collected from public pathway databases. Information is sourced from public pathway databases and is readily searched, visualized, and downloaded. The data is freely available under the license terms of each contributing database.