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Found 26 result(s)

Autism Chromosome Rearrangement Database

ACRD

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The Autism Chromosome Rearrangement Database is a collection of hand curated breakpoints and other genomic features, related to autism, taken from publicly available literature: databases and unpublished data.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.

Community Data Program

CDP

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The Community Data Program (CDP) is a membership-based community development initiative open to any Canadian public, non-profit or community sector organization with a local service delivery or public policy mandate. The program facilitates access to the evidence needed to tell our stories and inform effective and responsive policy and program design and implementation. The CDP makes data accessible and useful for all members with training and capacity building resources. Through its vibrant network, the CDP facilitates and supports dialogue and the sharing of best practices in the use of community data. The CDP has emerged as a unique Canada-wide platform for generating information, convening and collaborating.

National Earthquake DataBase

Base Nationale de Données Sismologiques

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The National Earthquake Database (NEDB) comprises a number of separate databases that together act as the national repository for all raw seismograph data, measurements, and derived parameters arising from the Canadian National Seismograph Network (CNSN), the Yellowknife Seismological Array (YKA), previous regional telemetered networks in eastern and western Canada (ECTN, WCTN), local telemetered networks (CLTN, SLTN), the Regional Analogue Network, and the former Standard Seismograph Network (CSN). It supports the efforts of Earthquakes Canada in Canadian seismicity monitoring, global seismic monitoring, verification of the Comprehensive nuclear Test Ban Treaty, and international data exchange. It also supports the Nuclear Explosion Monitoring project.

INDEPTH Data Repository

International Network for the Demographic Evaluation of Populations and Their Health Data Repository

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INDEPTH is a global network of research centres that conduct longitudinal health and demographic evaluation of populations in low- and middle-income countries (LMICs). INDEPTH aims to strengthen global capacity for Health and Demographic Surveillance Systems (HDSSs), and to mount multi-site research to guide health priorities and policies in LMICs, based on up-to-date scientific evidence. The data collected by the INDEPTH Network members constitute a valuable resource of population and health data for LMIC countries. This repository aims to make well documented anonymised longitudinal microdata from these Centres available to data users.

International Mouse Phenotyping Consortium

IMPC

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The IMPC is a confederation of international mouse phenotyping projects working towards the agreed goals of the consortium: To undertake the phenotyping of 20,000 mouse mutants over a ten year period, providing the first functional annotation of a mammalian genome. Maintain and expand a world-wide consortium of institutions with capacity and expertise to produce germ line transmission of targeted knockout mutations in embryonic stem cells for 20,000 known and predicted mouse genes. Test each mutant mouse line through a broad based primary phenotyping pipeline in all the major adult organ systems and most areas of major human disease. Through this activity and employing data annotation tools, systematically aim to discover and ascribe biological function to each gene, driving new ideas and underpinning future research into biological systems; Maintain and expand collaborative “networks” with specialist phenotyping consortia or laboratories, providing standardized secondary level phenotyping that enriches the primary dataset, and end-user, project specific tertiary level phenotyping that adds value to the mammalian gene functional annotation and fosters hypothesis driven research; and Provide a centralized data centre and portal for free, unrestricted access to primary and secondary data by the scientific community, promoting sharing of data, genotype-phenotype annotation, standard operating protocols, and the development of open source data analysis tools. Members of the IMPC may include research centers, funding organizations and corporations.

Canadian Biodiversity Information Facility

Système canadien d'information sur la biodiversité

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!!! <<< the repository is offline >>> !!! The CBIF provides primary data on biological species of interest to Canadians. CBIF supports a wide range of social and economic decisions including efforts to conserve our biodiversity in healthy ecosystems, use our biological resources in sustainable ways, and monitor and control pests and diseases. Tools provided by the CBIF include the Integrated Taxonomic Information System (ITIS), Species Access Network, Online Mapping, and the SpeciesBank, including Butterflies of Canada. The CBIF is a member of the Global Biodiversity Information Facility (GBIF).

Cystic Fibrosis Mutation Database

CFTR1

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The Cystic Fibrosis Mutation Database (CFTR1) was initiated by the Cystic Fibrosis Genetic Analysis Consortium in 1989 to increase and facilitate communications among CF researchers, and is maintained by the Cystic Fibrosis Centre at the Hospital for Sick Children in Toronto. The specific aim of the database is to provide up to date information about individual mutations in the CFTR gene. In a major upgrade in 2010, all known CFTR mutations and sequence variants have been converted to the standard nomenclature recommended by the Human Genome Variation Society.

Brain-CODE

Brain-Centre for Ontario Data Exploration

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Brain-CODE is a large-scale informatics platform that manages the acquisition and storage of multidimensional data collected from participants with a variety of brain disorders.

Westbank First Nation Open Data

WFN Open Data

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This open data portal includes datasets related to Westbank First Nation.

Journal of applied econometrics Data Archive

JAE Data Archive

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The JAE Data Archive, which is hosted by a server belonging to the Economics Department of Queen's University, contains data for all papers accepted after January, 1994, unless the data are confidential. There are also data for a few papers accepted earlier. Volume 10, No. 1 (1995) is the first issue in which all papers were accepted subject to the proviso that data be provided. For some papers, especially more recent ones, the Data Archive also contains programs and supplementary material, such as technical appendices and additional graphs.

NB Institute for Research, Data and Training

NB-IRDT

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NB-IRDT is expanding research potential through pseudonymised, linkable data sets. Our repository includes a growing collection to meet diverse research needs. We only host pseudonymous data in the NB-IRDT repository. NB-IRDT also offers public use data sets, which consist of de-identified data that is publicly accessible. All our data can be accessed in the NB-IRDT lab spaces.

Water Survey of Canada

Relevés hydrologiques du Canada

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Real time and archival databases containing Canadian water information. These data include, archived hydrometric data, water level and streamflow statistics, daily and monthly mean flow, water level and sediment concentration for monitoring station across Canada. The Water Survey of Canada (WSC) is the national authority responsible for the collection, interpretation and dissemination of standardized water resource data and information in Canada. In partnership with the provinces, territories and other agencies, WSC operates over 2800 active hydrometric gauges across the country.

District of Peachland Open Data

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Search, explore, and download open datasets sourced from the District of Peachland.

<odesi>

Initiative ontarienne en matière de documentation des données, de service d'extraction et d'infrastructure

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<odesi> is a digital repository for social science data, including polling data. Data collections are: Statistics Canada, Canadian Gallup Polls, CORA - Canadian Opinion Research Archive, ICPSR - Interuniversity Consortium for Political and Social Research.

Manitoba Population Research Data Repository

MCHP Data Repository

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The Population Health Research Data Repository housed at MCHP is a comprehensive collection of administrative, registry, survey, and other data primarily relating to residents of Manitoba. It was developed to describe and explain patterns of health care and profiles of health and illness, facilitating inter-sectoral research in areas such as health care, education, and social services.

Canadian Poisonous Plants Information System

Système canadien d'information sur les plantes toxiques

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!!! <<< the repository is offline >>> !!! The Canadian Poisonous Plants Information System presents data on plants that cause poisoning in livestock, pets, and humans. The plants include native, introduced, and cultivated outdoor plants as well as indoor plants that are found in Canada. Some food and herbal plants that may cause potential poisoning problems are also included.

VENUS in the Salish Sea

VENUS

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>>>!!!<<<VENUS coastal network, is now part of the Ocean Networks Canada Observatory>>>!!!<<< VENUS is a cabled undersea laboratory for ocean researchers and explorers. VENUS delivers real time information from seafloor instruments via fibre optic cables to the University of Victoria, BC. You can see ocean data live, recent and archived as well as learn more about on-going research

World Ozone and Ultraviolet Radiation Data Centre

Centre Mondial des Données sur l'Ozone et le Rayonnment Ultraviolet

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The WOUDC processes, archives and publishes world ozone and UV data reported by over 400 stations comprising over 100 international agencies and universities. The World Ozone and Ultraviolet Radiation Data Centre (WOUDC) has the two component parts: the World Ozone Data Centre (WODC) and the World Ultraviolet Radiation Data Centre (WUDC). These data are available on-line with updates occuring every week and in addition to the on-line archive, data are published annually on CD-ROM, now DVD.

Pseudomonas Genome DB

Pseudomonas Genome Database

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The Pseudomonas Genome Database collaborates with an international panel of expert Pseudomonas researchers to provide high quality updates to the PAO1 genome annotation and make cutting edge genome analysis data available.

Altalis

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Established in 1998, we have been the authoritative source of spatial data and imagery in Alberta for over 20 years. We have a joint venture agreement with Alberta Data Partnerships Ltd. (ADP) and are responsible for the day-to-day management and distribution of the digital data sets they manage. As the agent for ADP, we are responsible for making mapping products available, accessible, accurate and affordable. We are the leading data management, maintenance, and distribution company in Alberta, and ensure the continued updating, re-engineering, storage, distribution, value-added redistribution, and general management of primary provincial mapping datasets. Our webstore, Altalis.com, enables customers to explore, view, and acquire spatial data products both paid and open data with the click of a button. We take pride in providing exceptional customer service and building long-term relationships with our clients. Our experienced customer service team are available to answer any questions you may have about finding the right data to meet your needs.

BORN Ontario

Better Outcomes Registry & Network

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The Better Outcomes Registry & Network (BORN) is Ontario's prescribed perinatal, newborn and child registry with the role of facilitating quality care for families across the province. BORN collects, interprets, shares and rigorously protects high-quality data essential to making Ontario the safest place in the world to have a baby.

Toronto and Region Conservation Authority Open Data

TRCA Open Data

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With more than 60 years of experience, Toronto and Region Conservation Authority (TRCA) is one of 36 Conservation Authorities in Ontario, created to safeguard and enhance the health and well-being of watershed communities through the protection and restoration of the natural environment and the ecological services the environment provides. At TRCA, we are working towards providing free and open access to our data and information, in both accessible and machine readable formats, to ensure it’s available and easy to consume. Improving access to TRCA’s data and information will provide transparency into the decision making process and will improve accountability while increasing the public’s understanding and engagement with the organization.

Population Data BC

PopData

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Population Data BC (PopData) is a multi-university, data and education resource facilitating interdisciplinary research on the determinants of human health, well-being and development. Providing a range of services to researchers and data providers, PopData strives to ensure that researchers have timely access to the data and training they need to address research questions on population health. Research using these data informs policy-making and leads to healthier communities.

Database of Genomic Variants

DGV

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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.

Cancer in Young People in Canada

CYP-C

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The Cancer in Young People in Canada (CYP-C) surveillance program collects in-depth data concerning risk factors, health outcomes, quality and accessibility of care, and late effects among children and youth with cancer. CYP-C represents a collaboration involving the C17 Council, Canadian Partnerships Against Cancer (CPAC), Public Health Agency of Canada (PHAC), provincial and territorial cancer registries, Statistics Canada and non-governmental organizations.