These methods still result in each protein being assigned a single label.
The experiments on CASIA show that despite neglecting detailed texture information, our method still provides results comparable to those of recent methods.
Note that a smaller number of potential locations were allowed for smaller display sizes, however even the method used still results in relatively greater variation when fewer bars were present.
Even when the individual dataset is relatively large compared to the literature, the proposed method will still result in an estimate closer to the underlying multivariable association than the standard method ignoring the literature.
Especially for factory1 and machinegun noises, the proposed method still obtains good results while some other VAD methods seem to exhibit worse performance nearly close to random guess.
Although this is the most severe test of the penalization (due to the global support of the Fourier basis), it is shown that the method still yields reasonable results.
When only two seed terms are used, the method still produces satisfactory results, but recall and precision drop to 68.2% and 51.5%, respectively.
Although the allele specific qPCR is an efficient closed-tube procedure for mutation identification, this fluorescent based method still costs false positive results [ 9].
Though these probes only represent a sparse sampling on every transcript in the transcriptome, the method still provides reasonably accurate results.
