Averages over smooth measures on smooth compact hypersurfaces in$R$^{$n$}are studied. With assumptions on the decay of the Fourier transform of the measure we obtain mixed norm estimates for these means, for example$L$^{$p$}estimates of multiparameter maximal functions over compact hypersurfaces.

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We show that the transition probability of the Markov chain ($G$($i$,1),...,$G$($i$,$n$))_{$i$≥1}, where the$G$($i$,$j$)’s are certain directed last-passage times, is given by a determinant of a special form. An analogous formula has recently been obtained by Warren in a Brownian motion model. Furthermore we demonstrate that this formula leads to the Meixner ensemble when we compute the distribution function for$G$($m$,$n$). We also obtain the Fredholm determinant representation of this distribution, where the kernel has a double contour integral representation.

There are few techniques available for testing whether or not a family of parametric times series models fits a set of data reasonably well without serious restrictions on the forms of alternative models. In this paper, we consider generalised likelihood ratio tests of whether or not the spectral density function of a stationary time series admits certain parametric forms. We propose a bias correction method for the generalised likelihood ratio test of Fan et al. (2001). In particular, our methods can be applied to test whether or not a residual series is white noise. Sampling properties of the proposed tests are established. A bootstrap approach is proposed for estimating the null distribution of the test statistics. Simulation studies investigate the accuracy of the proposed bootstrap estimate and compare the power of the various ways of constructing the generalised likelihood ratio tests as well as some classic methods like

DNA microarray analysis has emerged as a leading technology to enhance our understanding of gene regulation and function in cellular mechanism controls on a genomic scale. This technology has advanced to unravel the genetic machinery of biological rhythms by collecting massive gene-expression data in a time course. Here, we present a statistical model for clustering periodic patterns of gene expression in terms of different transcriptional profiles. The model incorporates biologically meaningful Fourier series approximations of gene periodic expression into a mixture-model-based likelihood function, thus producing results that are likely to be closer to biological relevance, as compared to those from existing models. Also because the structures of the time-dependent means and covariance matrix are modeled, the new approach displays increased statistical power and precision of parameter estimation. The