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Difference of Gaussians

Extraction of extrema of image intensity over all scales and image locations is implemented by using a difference-of-Gaussian function to identify potential candidates of Pols. [Pg.124]

This paper uses a performance measure based on EER ratio. The number of Gaussian was fixed from 64,128 and 256 for the imposter model. This is because to investigate the effect of the difference of Gaussian s imposter on the accuracy. Again the training iteration was fixed to 20 times for imposter and 15 for the client model. [Pg.562]

Masking the difference of Gaussian channel also reduces fluorescence cross talk between nonoverlapping puncta. Importantly, the difference of Gaussians should be applied to a copy of the post-processed channel because the created data will no longer be quantifiable. Once a mask is made for the difference of Gaussian channel, it is copied back onto the original post-processed channel to extract quantifiable information. [Pg.267]

Figure Al.6.30. (a) Two pulse sequence used in the Tannor-Rice pump-dump scheme, (b) The Husuni time-frequency distribution corresponding to the two pump sequence in (a), constmcted by taking the overlap of the pulse sequence with a two-parameter family of Gaussians, characterized by different centres in time and carrier frequency, and plotting the overlap as a fiinction of these two parameters. Note that the Husimi distribution allows one to visualize both the time delay and the frequency offset of pump and dump simultaneously (after [52a]). Figure Al.6.30. (a) Two pulse sequence used in the Tannor-Rice pump-dump scheme, (b) The Husuni time-frequency distribution corresponding to the two pump sequence in (a), constmcted by taking the overlap of the pulse sequence with a two-parameter family of Gaussians, characterized by different centres in time and carrier frequency, and plotting the overlap as a fiinction of these two parameters. Note that the Husimi distribution allows one to visualize both the time delay and the frequency offset of pump and dump simultaneously (after [52a]).
A different approach is to represent the wavepacket by one or more Gaussian functions. When using a local harmonic approximation to the trae PES, that is, expanding the PES to second-order around the center of the function, the parameters for the Gaussians are found to evolve using classical equations of motion [22-26], Detailed reviews of Gaussian wavepacket methods are found in [27-29]. [Pg.253]

We ll look at the main features of this output now. Locate the corresponding section in your file with your editor as you read each comment. Note that the output from your system may vary slightly. Not every numerical value will necessarily agree to the last decimal place, although differences should appear only beyond the fifth decimal place. This subsection concludes the Gaussian tutorial.Once you have completed it, you will be ready to learn about the various types of Gaussian jobs as well as the model chemistries the program offers. [Pg.337]

Fig. 13. Calculated 2H solid echo spectra for log-Gaussian distributions of correlation times of different widths. Note the differences of the line shapes for fully relaxed and partially relaxed spectra. The centre of the distribution of correlation times is given as a normalized exchange rate a0 = 1/3tc. For deuterons in aliphatic C—H bonds the conversion factor is approximately 4.10s sec-1... Fig. 13. Calculated 2H solid echo spectra for log-Gaussian distributions of correlation times of different widths. Note the differences of the line shapes for fully relaxed and partially relaxed spectra. The centre of the distribution of correlation times is given as a normalized exchange rate a0 = 1/3tc. For deuterons in aliphatic C—H bonds the conversion factor is approximately 4.10s sec-1...
The two expansions discussed so far appear to be quite different. In the multistate Gaussian model, different functions are centered at different values of AU. In the Gram-Charlier expansion, all terms are centered at (AU)0. The difference, however, is smaller that it appears. In fact, one can express a combination of Gaussian functions in the form of (2.56) taking advantage of the addition theorem for Hermite polynomials [44], Similarly, another, previously proposed representation of Pq(AU) as a r function [45] can also be transformed into the more general form of (2.56). [Pg.65]

At this stage we are at the very beginning of development, implementation, and application of methods for quantum-mechanical calculations of molecular systems without assuming the Born-Oppenheimer approximation. So far we have done several calculations of ground and excited states of small diatomic molecules, extending them beyond two-electron systems and some preliminary calculations on triatomic systems. In the non-BO works, we have used three different correlated Gaussian basis sets. The simplest one without r,y premultipliers (4)j = exp[—r (A t (8> Is) "]) was used in atomic calculations the basis with premultipliers in the form of powers of rj exp[—r (Aj (8> /sjr])... [Pg.470]


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