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Exact(5)
Previously described methods have either involved construction of a custom rail in the radiography department [10] or augmentation of the frame with a spirit level device [9].
The above NSS-based CS methods have either high complexity or low performance, especially in the case of low signal-to-noise ratio (SNR) regime.
However, the reported methods have either two distinct seeding sources or a tedious two-step fabrication route which requires the use of a catalyst to provide initial nucleation sites for growth of both CNTs and diamond.
To cope with this problem, previous methods have either considered only orthologues [9] or implemented a scoring system based on the frequencies of domain families in the whole target sequence database [7].
Previous Phylogenetic profiling methods have either used protein vectors comprised of binary values (i.e. homolog = 1, no homolog = 0) [ 4] or vectors normalized with E-values [ 7, 24].
Similar(55)
Although current high- resolution imaging techniques provide ample information, the analysis methods for localization have either been qualitative or employed quantification in non-randomly selected regions of interest.
Multilayer Bragg mirrors, in particular, have been modelled by the Transfer Matrix method, designed to have either near-UV or near-IR reflectivity, but visible transparency, based on alternating aluminosilicate glass/titania quarter-wave stacks.
However, these methods have limitations either due to patient discomfort, accuracy or ease of use.
A key feature of current Purkinje structural models is that their construction was designed or guided by the modeler; all current methods have used either hand-drawn or computer-generated networks that were created to follow general principles characteristic of Purkinje networks.
Similarly, the majority of methods for cDNA sequencing have either used polyA+ selected RNA and/or amplification for library construction, both of which selectively omit significant amounts of RNA and, hence, cannot accurately reflect the profile of all cellular RNAs.
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