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The NCBI Short Genetic Variations database, commonly known as dbSNP, catalogs short variations in nucleotide sequences from a wide range of organisms. These variations include single nucleotide variations, short nucleotide insertions and deletions, short tandem repeats and microsatellites. Short Genetic Variations may be common, thus representing true polymorphisms, or they may be rare. Some rare human entries have additional information associated withthem, including disease associations, genotype information and allele origin, as some variations are somatic rather than germline events. ***NCBI will phase out support for non-human organism data in dbSNP and dbVar beginning on September 1, 2017***
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depositar — taking the term from the Portuguese/Spanish verb for to deposit — is an online repository for research data. The site is built by the researchers for the researchers. You are free to deposit, discover, and reuse datasets on depositar for all your research purposes.
The Government is releasing public data to help people understand how government works and how policies are made. Some of this data is already available, but data.gov.uk brings it together in one searchable website. Making this data easily available means it will be easier for people to make decisions and suggestions about government policies based on detailed information.
The NASA Exoplanet Archive collects and serves public data to support the search for and characterization of extra-solar planets (exoplanets) and their host stars. The data include published light curves, images, spectra and parameters, and time-series data from surveys that aim to discover transiting exoplanets. Tools are provided to work with the data, particularly the display and analysis of transit data sets from Kepler and CoRoT. All data are validated by the Exoplanet Archive science staff and traced to their sources. The Exoplanet Archive is the U.S. data portal for the CoRoT mission.