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Most of ResearchGate's users are involved in medicine or biology, [10] [12] though it also has participants from engineering, law, computer science, agricultural sciences, and psychology, among others. [10] ResearchGate published an author-level metric in the form of an "RG Score" since 2012. [15] RG score is not a citation impact measure.
All data sourced from a third party to organization's internal teams may undergo accuracy (DQ) check against the third party data. These DQ check results are valuable when administered on data that made multiple hops after the point of entry of that data but before that data becomes authorized or stored for enterprise intelligence.
The clinical data manager is involved in early discussions about data collection options and then oversees development of data collection tools based on the clinical trial protocol. Once subject enrollment begins, the data manager ensures that data are collected, validated, complete, and consistent.
The advent of eHealth and advances in health information technology, however, have expanded the collection and use of health data—but have also engendered new security, privacy, and ethical concerns. [3] The increasing collection and use of health data by patients is a major component of digital health.
Cleverdon’s experiments established a number of key aspects required for IR evaluation: a test collection, a set of queries and a set of pre-determined relevant items which combined would determine precision and recall. Cleverdon's approach formed a blueprint for the successful Text Retrieval Conference series that began in 1992.
In addition, they may apply the science of informatics to the collection, storage, analysis, use, and transmission of information to meet legal, professional, ethical and administrative records-keeping requirements of health care delivery. [1] They work with clinical, epidemiological, demographic, financial, reference, and coded healthcare data.
The researchers analyzed historical data on childhood blood-lead levels, leaded gas use and U.S. population statistics, determining that more than 170 million Americans had "clinically concerning ...
In cases in which a physician has difficulty explaining complicated medical concepts to a patient, that patient may be inclined to seek information on the internet. [8] A consensus exists that patients should have shared decision making, meaning that patients should be able to make informed decisions about the direction of their medical treatment in collaboration with their physician. [9]