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In contrast to screening for the loss of lacZα function, fluorescent protein-based screening is based on a gain of fluorescence that can increase screening fidelity as the fluorescence property cannot be acquired spontaneously.
The contemporary standard approach for ligand-based virtual screening is based on a sequential screening pipeline which means that every compound of a given compound library has to be screened against a reference molecule.
Most of what we know about breast cancer screening is based on studies of white European women.
This approach to screening is based on the detection of biomarkers (physiological or molecular changes) that are characteristic of common infectious diseases, cancers, and other disorders.
The screening is based on the observation of physiologic variations using ratios of relative amounts: lipid/DNA and lipid/protein.
One common class of solutions to perform virtual screening is based on target prediction approaches that have been addressed by several studies [7 10].
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The task force's decision to recommend later and less-frequent screening was based on research into the benefits and risks of mammography.
The screening was based on their discharge, solubility, toxicity and volatility.
The selection of drugs for screening was based on frequency of detection in WADA reports over the past five years [28].
The first screening was based on βgal expression.
The first-stage screening was based on the MMSE.
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