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Quantitative and categorical data derived from the multiple sorting methods were subjected to multidimensional scaling analysis.
The extracts with higher yield from both methods were subjected to transesterification and GC MS analysis.
Samples from both sea shells each of them prepared by the above mentioned methods were subjected to thermal treatments at 450 °C and 850 °C in order to evaluate the crystalline transformations of the calcium phosphate structures in the heating process.
The raw data obtained from 454 sequencing of the target enriched DNA (see Methods) were subjected to an analysis and filter process depicted in Figure 1.
Four probe sets, representing genes putatively involved in the fatty acid metabolism (listed in Methods) were subjected to real-time qRT-PCR analysis to validate the microarray data.
The sequences not amplifiable by the above PCR methods were subjected to PCR with primers deduced from adjacent 5′ and 3′ sequences.
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However, these methods are subjected to significant delays when implemented in real-time gait monitoring devices, orthoses, and FES systems.
All populations of both selection methods are subjected to 5000 generations of selective pressure withdrawal to simulate the disuse of specific antibiotics after prevalence of resistance.
Both methods are subjected to permutation tests in order to establish per protein the significance of its distribution of CTL epitopes.
HUVEC microtissues (MTs), synthesized via hanging drop method, were subjected to angiogenesis in GTC-human fibrin (HF) hydrogels.
Five half-scale test specimens of battened members designed as per the current practice and improved design method were subjected to axial load and gradually increasing cyclic load.
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