This method thus requires feature and/or label space transformations to bridge the gap for knowledge transfer, as well as handling the cross-domain data distribution differences.
Each conformational sampling method thus requires its own reference state and corresponding reference distribution; this is likely the main reason behind the large number of different reference states reported in the literature [3], [22], [38] [41].
These methods thus require months of culture to generate sufficient cell numbers for feasibility studies in a lab setting and the cell populations often have reduced proliferation and differentiation potential, or have become immortalized cells.
Both of these methods thus require that the instrument be administered via computer.
A regularization method is thus required.
A sensitive, simple, and validated analytical method is thus required to monitor the reaction and its components, especially the MEG content.
Biological processes consist of many interacting components, exceeding the human capacity to systematically analyze them, thus requiring methods to reduce the complexity and thereby enhance their accessibility [1].
Modern analytic methods have increased sensitivity, thus requiring smaller sample volumes, which are easier to obtain.
Reliable methods are thus required that provide accurate scaling rules for dynamic similarity between models and prototypes.
Other methods are thus required to measure EVLW directly.
