On empirical density function

1972 ◽  
Vol 2 (1-4) ◽  
pp. 85-110 ◽  
Author(s):  
P. Révész
1976 ◽  
Vol 15 (02) ◽  
pp. 94-98 ◽  
Author(s):  
G. Ferber ◽  
G. Eichholz

For 1000 variables extracted from auto- and cross-spectra of two 12-channel montages, the empirical density function is investigated. Only a small group of them may be considered to have a univariate normal distribution. Another important group including the absolute and the relative power in the four classical frequency bands has distribution functions that may be more or less accurately approximated by gamma-type functions.A third group including some of the peak frequencies shows distribution functions with two peaks not assignable to any natural classification of the EEG.The power of discrimination between the four samples is investigated for each variable by means of Bayes-classification and by a quasi-Kolmogorov-statistic. Its quality is demonstrated using linear discriminant analysis.Correlations were computed to complete basic statistical information.


2016 ◽  
Vol 37 (1) ◽  
Author(s):  
Eugenia Stoimenova

This paper is concerned with the nonparametric estimation of a density function when the data are incomplete due to interval censoring. The Nadaraya-Watson kernel density estimator is modified to allow description of such interval data. An interactive R application is developed to explore different estimates.


Author(s):  
David Cockayne ◽  
David McKenzie

The technique of Electron Reduced Density Function (RDF) analysis has ben developed into a rapid analytical tool for the analysis of small volumes of amorphous or polycrystalline materials. The energy filtered electron diffraction pattern is collected to high scattering angles (currendy to s = 2 sinθ/λ = 6.5 Å-1) by scanning the selected area electron diffraction pattern across the entrance aperture to a GATAN parallel energy loss spectrometer. The diffraction pattern is then converted to a reduced density function, G(r), using mathematical procedures equivalent to those used in X-ray and neutron diffraction studies.Nearest neighbour distances accurate to 0.01 Å are obtained routinely, and bond distortions of molecules can be determined from the ratio of first to second nearest neighbour distances. The accuracy of coordination number determinations from polycrystalline monatomic materials (eg Pt) is high (5%). In amorphous systems (eg carbon, silicon) it is reasonable (10%), but in multi-element systems there are a number of problems to be overcome; to reduce the diffraction pattern to G(r), the approximation must be made that for all elements i,j in the system, fj(s) = Kji fi,(s) where Kji is independent of s.


2015 ◽  
Vol 47 (8) ◽  
pp. 24-40 ◽  
Author(s):  
Telman Abbas ogly Aliev ◽  
Naila F. Musaeva ◽  
Matanat Tair kyzy Suleymanova ◽  
Bahruz Ismail ogly Gazizade

2016 ◽  
Vol 48 (4) ◽  
pp. 39-55 ◽  
Author(s):  
Telman Abbas ogly Aliev ◽  
Naila Fuad kyzy Musaeva ◽  
Matanat Tair kyzy Suleymanova ◽  
Bahruz Ismail ogly Gazizade

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