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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***
The project is set up in order to improve the infrastructure for text-based linguistic research and development by building a huge, automatically annotated German text corpus and the corresponding tools for corpus annotation and exploitation. DeReKo constitutes the largest linguistically motivated collection of contemporary German texts, contains fictional, scientific and newspaper texts, as well as several other text types, contains only licenced texts, is encoded with rich meta-textual information, is fully annotated morphosyntactically (three concurrent annotations), is continually expanded, with a focus on size and stratification of data, may be analyzed free of charge via the query system COSMAS II, serves as a 'primordial sample' from which users may draw specialized sub-samples (socalled 'virtual corpora') to represent the language domain they wish to investigate. !!! Access to data of Das Deutsche Referenzkorpus is also provided by: IDS Repository https://www.re3data.org/repository/r3d100010382 !!!
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The Climate Change Centre Austria - Data Centre provides the central national archive for climate data and information. The data made accessible includes observation and measurement data, scenario data, quantitative and qualitative data, as well as the measurement data and findings of research projects.