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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 ...
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
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 ...
A gateway to government science information and research results. Science.gov provides a search of over 45 scientific databases and 200 million pages of science information with just one query, and is a gateway to over 2000 scientific Websites. Free
There is broad consensus that when a person donates a specimen for research then that person has a right to privacy thereafter. To this end, researchers balance the need for specimens to be anonymous or de-identified from protected health information with the need to have access to data about the specimen so that researchers can use the sample without knowing the identity of the donor. [7]
12 languages. العربية ... In other projects Wikimedia Commons; Wikidata item; Appearance. move to sidebar hide. ... Biobanks (4 C, 12 P) Biological databases ...