Search results
Results from the WOW.Com Content Network
In 2008, United States researchers stored 270 million specimens in biobanks, and the rate of new sample collection was 20 million per year. [11] These numbers represent a fundamental worldwide change in the nature of research between the time when such numbers of samples could not be used and the time when researchers began demanding them. [11]
Also biobanks, which do specimen storage, cannot take full responsibility for specimen integrity, because before they take custody of samples someone must collect and process them and effects such as RNA degradation are more likely to occur from delayed sample processing than inadequate storage.
The National Institute on Aging (NIA) Aging Cell Repository facilitates research into the mechanisms of aging by providing cell lines collected from subjects of different ages. [ 9 ] [ 8 ] The National Institute of General Medical Sciences (NIGMS) Human Genetic Cell Repository is collection of well-characterized human cells for use in ...
A biobank is a physical place which stores biological specimens.In some cases, participant data is also collected and stored. Access policies details may vary across biobanks but generally involve obtaining ethics approval from institutional review boards (IRB) and scientific review or peer review approval from the institutions under which the biobanks operate as well as Ethics approval from ...
server and repository for protein structure models Protein model databases AAindex: database of amino acid indices, amino acid mutation matrices, and pair-wise contact potentials Protein model databases BioGRID: Samuel Lunenfeld Research Institute: general repository for interaction datasets Protein-protein and other molecular interactions
Medicine, healthcare: Easy-to-use interface to search and retrieve citations and abstracts for biomedical and health journals. Subscription EBSCO [97] MedlinePlus: Medicine: Free Produced by the United States National Library of Medicine, the United States National Institutes of Health, and the United States Department of Health and Human ...
The use of Clinical Data Repositories could provide a wealth of knowledge about patients, their medical conditions, and their outcome. The database could serve as a way to study the relationship and potential patterns between disease progression and management. The term "Medical Data Mining" has been coined for this method of research.
One was the advent of biobanks, which are repositories of human genetic material that greatly reduced the cost and difficulty of collecting sufficient numbers of biological specimens for study. [12] Another was the International HapMap Project , which, from 2003 identified a majority of the common SNPs interrogated in a GWA study. [ 13 ]