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Found 5 result(s)
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Institutional research data repository of Riga Technical University (RTU). The aim is to collect and store scientific research data and other relevant information in all fields of knowledge of RTU, enabling free, easy and convenient access to it.
BeiDare2 is currently at beta version. All new users should try the new service as we no longer provide training for the classic BioDare. - BioDare stands for Biological Data Repository, its main focus is data from circadian experiments. BioDare is an online facility to share, store, analyse and disseminate timeseries data, focussing on circadian clock data, with browser and web service interfaces. Toolbox features include an improved, speedier FFT-NLLs routine and ROBuST’s Spectrum Resampling tool that will analyse rhythmic time series data.
The eyeGENE® Research Resource is open for approved research studies. Application details here Researchers and clinicians are actively developing gene-based therapies to treat ophthalmic genetic diseases that were once considered untreatable.
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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.
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The Human Genetic Variation Database (HGVD) aims to provide a central resource to archive and display Japanese genetic variation and association between the variation and transcription level of genes. The database currently contains genetic variations determined by exome sequencing of 1,208 individuals and genotyping data of common variations obtained from a cohort of 3,248 individuals.