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Found 9 result(s)
The Scholarly Database (SDB) at Indiana University aims to serve researchers and practitioners interested in the analysis, modeling, and visualization of large-scale scholarly datasets. The online interface provides access to six datasets: MEDLINE papers, registered Clinical Trials, U.S. Patent and Trademark Office patents (USPTO), National Science Foundation (NSF) funding, National Institutes of Health (NIH) funding, and National Endowment for the Humanities funding – over 26 million records in total.
All ADNI data are shared without embargo through the LONI Image and Data Archive (IDA), a secure research data repository. Interested scientists may obtain access to ADNI imaging, clinical, genomic, and biomarker data for the purposes of scientific investigation, teaching, or planning clinical research studies. "The Alzheimer’s Disease Neuroimaging Initiative (ADNI) unites researchers with study data as they work to define the progression of Alzheimer’s disease (AD). ADNI researchers collect, validate and utilize data, including MRI and PET images, genetics, cognitive tests, CSF and blood biomarkers as predictors of the disease. Study resources and data from the North American ADNI study are available through this website, including Alzheimer’s disease patients, mild cognitive impairment subjects, and elderly controls. "
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The New York Brain Bank (NYBB) at Columbia University was established to collect postmortem human brains to meet the needs of neuroscientists investigating specific psychiatric and neurological disorders.
The Growing Up Today Study is a collaborative study between clinicians, researchers, and thousands of participants across the US and beyond. The aim of this study is to gain a deeper understanding of the factors that affect health throughout life. Together we are working to building one of the most powerful resources for fighting cancer, obesity, heart disease, depression, and so much more.
The twin GRACE satellites were launched on March 17, 2002. Since that time, the GRACE Science Data System (SDS) has produced and distributed estimates of the Earth gravity field on an ongoing basis. These estimates, in conjunction with other data and models, have provided observations of terrestrial water storage changes, ice-mass variations, ocean bottom pressure changes and sea-level variations. This portal, together with PODAAC, is responsible for the distribution of the data and documentation for the GRACE project.
TerraSAR-X is a German satellite for Earth Observation, which was launched on July 14, 2007. The mission duration was foreseen to be 5 years. TerraSAR-X carries an innovative high resolution x-band sensor for imaging with resolution up to 1 m. TerraSAR-X carries as secondary payload an IGOR GPS receiver with GPS RO capability. GFZ provided the IGOR and is responsible for the related TOR experiment (Tracking, Occultation and Ranging). TerraSAR-X provides continuously atmospheric GPS data in near-real time. These data from GFZ are continuously assimilated in parallel with those from GRACE-A by the world-leading weather centers to improve their global forecasts. TerraSAR-X, together with TanDEM-X also forms a twin-satellite constellation for atmosphere sounding and generates an unique data set for the evaluation of the accuracy of the GPS-RO technique.
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The Visible Human Project® is an outgrowth of the NLM's 1986 Long-Range Plan. It is the creation of complete, anatomically detailed, three-dimensional representations of the normal male and female human bodies. Acquisition of transverse CT, MR and cryosection images of representative male and female cadavers has been completed. The male was sectioned at one millimeter intervals, the female at one-third of a millimeter intervals.
This database contains individual-based life history data that have been collected from wild primate populations by nine working group participants over a minimum of 19 years.
The National Trauma Data Bank® (NTDB) is the largest aggregation of trauma registry data ever assembled. The goal of the NTDB is to inform the medical community, the public, and decision makers about a wide variety of issues that characterize the current state of care for injured persons. Registry data that is collected from the NTDB is compiled annually and disseminated in the forms of hospital benchmark reports, data quality reports, and research data sets. Research data sets that can be used by researchers. To gain access to NTDB data, researchers must submit requests through our online application process