Abstract:The problem of interaction in multidime nsional co ntin ge ncy tables is inves ti gated from the viewpoint of information th eory as developed by Kullbac k. The hypothesis of no rth-order interaction is defin ed in the sense of an hypothes is of "generalized " ind ependence of classifications with fix ed rth order marginal restraints. For a three· way table, with given cell probabilities 7Tijk , the minimum discrimination information for a contin ge ncy table with marginals P jj ., P. jk, and P i ... is given … Show more
“…By inspection of the data and Table 4, it was possible to eliminate interactions roughly in the order in which their deletion would least affect goodness of fit. After each elimination, the difference between models was evaluated for significance according to the method of partitioning expounded in Kullback ( 1959) and Ku and Kullback ( 1968). In this approach, the difference between the log-likelihood ratio chi-squares for the two models can be used to test the hypothesis that the difference between expected values for the two models is due to random variation.…”
Section: Resultsmentioning
confidence: 99%
“…Both these statistics have the same y! distribution for sample sizes large enough, where the degrees of freedom are computed in the way described by Ku and Kullback (1968) or by Fienberg in the article immediately following this one. In four of the five sets of data, the models containing all two-factor interactions gave satisfactory fits at the 5% level or better as judged by both these criteria (Table 5) .…”
Abstract. Sympatric native Anolis species with similar structural habitats but contrasting climatic habitats are closer in head and body size on species-rich than on depauperate islands.In two localities, sympatric Anolis species with differential occurrences in sun or shade sought lower, more shaded perches during midday, resulting in partly nonsynchronous utilization of the vegetation by the two species.The second observation may be related to the first in the following way : nonsynchronous spatial overlap could dictate relatively great resource overlap for species coinhabiting patchy or edge areas, requiring great differences between the species in prey size in addition to those in climatic habitat. The extent of such overlap on small depauperate islands could be greater if these contained a greater proportion of patchy or edge habitats (with respect to insolation), or if climatic preferences were broader and more overlapping than on large, species-rich islands.In each locality, the relatively more shade-inhabiting species occurred more often on larger perches and on lower perches than did the other species. In both species of the Bermudan pair, adult males occupied higher and larger perches, and in grahami, shadier perches, than did female-sized individuals. The statistical significance of these and other differences was evaluated using several unweighted "1..2 procedures, Cochran's weighted "1..2 test and a partitioning technique for analyzing interactions among variables in complex contingency tables. The last method is described in detail in the paper by Fienberg, immediately following this one.
“…By inspection of the data and Table 4, it was possible to eliminate interactions roughly in the order in which their deletion would least affect goodness of fit. After each elimination, the difference between models was evaluated for significance according to the method of partitioning expounded in Kullback ( 1959) and Ku and Kullback ( 1968). In this approach, the difference between the log-likelihood ratio chi-squares for the two models can be used to test the hypothesis that the difference between expected values for the two models is due to random variation.…”
Section: Resultsmentioning
confidence: 99%
“…Both these statistics have the same y! distribution for sample sizes large enough, where the degrees of freedom are computed in the way described by Ku and Kullback (1968) or by Fienberg in the article immediately following this one. In four of the five sets of data, the models containing all two-factor interactions gave satisfactory fits at the 5% level or better as judged by both these criteria (Table 5) .…”
Abstract. Sympatric native Anolis species with similar structural habitats but contrasting climatic habitats are closer in head and body size on species-rich than on depauperate islands.In two localities, sympatric Anolis species with differential occurrences in sun or shade sought lower, more shaded perches during midday, resulting in partly nonsynchronous utilization of the vegetation by the two species.The second observation may be related to the first in the following way : nonsynchronous spatial overlap could dictate relatively great resource overlap for species coinhabiting patchy or edge areas, requiring great differences between the species in prey size in addition to those in climatic habitat. The extent of such overlap on small depauperate islands could be greater if these contained a greater proportion of patchy or edge habitats (with respect to insolation), or if climatic preferences were broader and more overlapping than on large, species-rich islands.In each locality, the relatively more shade-inhabiting species occurred more often on larger perches and on lower perches than did the other species. In both species of the Bermudan pair, adult males occupied higher and larger perches, and in grahami, shadier perches, than did female-sized individuals. The statistical significance of these and other differences was evaluated using several unweighted "1..2 procedures, Cochran's weighted "1..2 test and a partitioning technique for analyzing interactions among variables in complex contingency tables. The last method is described in detail in the paper by Fienberg, immediately following this one.
“…This is a special case of an approximation algorithm proposed by Kullback et al (Gokhale andKullback 1978: Ireland andKullback 1968;Ku andKullback 1969: Kullback 1948) for the purpose of hypothesis lesting in multidimensiomd conlingency tables. A detailed treatment of this kind of algorithm can be found in Bishop el al.…”
Section: Appendixmentioning
confidence: 99%
“…10.2 and 10.2-1). We presenl the ilerative solution given m Ku andKullback (1968, 1969) and Csiszfir (1975),concentrating on the case k 2, which is of interest for us. With all second-order marginals lixed, p* is obtained as the limit of the iterates described by the equations:…”
We propose a formal framework for the description of interactions among groups of neurons. This framework is not restricted to the common case of pair interactions, but also incorporates higher-order interactions, which cannot be reduced to lower-order ones. We derive quantitative measures to detect the presence of such interactions in experimental data, by statistical analysis of the frequency distribution of higher-order correlations in multiple neuron spike train data. Our first step is to represent a frequency distribution as a Markov field on the minimal graph it induces. We then show the invariance of this graph with regard to changes of state. Clearly, only linear Markov fields can be adequately represented by graphs. Higher-order interdependencies, which are reflected by the energy expansion of the distribution, require more complex graphical schemes, like constellations or assembly diagrams, which we introduce and discuss. The coefficients of the energy expansion not only point to the interactions among neurons but are also a measure of their strength. We investigate the statistical meaning of detected interactions in an information theoretic sense and propose minimum relative entropy approximations as null hypotheses for significance tests. We demonstrate the various steps of our method in the situation of an empirical frequency distribution on six neurons, extracted from data on simultaneous multineuron recordings from the frontal cortex of a behaving monkey and close with a brief outlook on future work.
“…Therefore, we ought to deal with the incomplete information as the latest true marginal probabilities, and we update the prior probabilities subject to the specified marginal probability restriction such that discrimination information between the prior and the posterior probabilities is minimized. Ku and Kullback (1968) and Ireland and Kullback (1968) discussed an updating method for saturated models of contingency tables based on minimum discrimination information . In this paper, we shall extend their method to log-linear models , discuss localization of global updating, and we shall show that Deming and Stephan's iterative procedure can be used to find the posterior probabilities.…”
A probability-updating method in probabilistic expert systems is considered in this paper based on minimum discrimination information. Here, newly acquired information is taken as the latest true marginal probabilities, not as observed data with the same weight as previous data. Posterior probabilities are obtained by updating prior probabilities subject to the latest true marginals. To apply this updating method to probabilistic expert systems, we extend Ku and Kullback(1968)'s minimum discrimination information method for saturated models to log-linear models, discuss localization of global updating, and show that Deming and Stephan's iterative procedure can be used to find the posterior probabilities. Our updating method can also be used to handle uncertain evidence in probabilistic expert systems.
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