\documentclass[11pt]{article} \setlength{\oddsidemargin}{0.0truein} \setlength{\evensidemargin}{0.0truein} \setlength{\textwidth}{6.5truein} \setlength{\topmargin}{0.0truein} \setlength{\textheight}{9.0truein} \setlength{\headsep}{0.0truein} \setlength{\headheight}{0.0truein} \setlength{\topskip}{10.0pt} \setlength{\parskip}{5mm} \usepackage{url} \begin{document} \begin{center} \textbf{\textsc{STANFORD UNIVERSITY}}\\[5pt] \textbf{\textsc{DEPARTMENT OF STATISTICS}}\\[5pt] \Large{\textbf\textsc{{DEPARTMENTAL SEMINAR}}} \end{center} \begin{center} 4:15 p.m., Tuesday, February 14, 2006\\ Sequoia Hall Room 200\\ (Cookies at 3:45 in 1st Floor Lounge) \end{center} \begin{center} \textsl{Yehua Li} \\ Department of Statistics\\ Texas A\&M University\\ \end{center} \begin{center} \textbf{Nonparametric Estimation of Correlation Functions \\ In Longitudinal And Spatial Data, With Application To \\ Colon Carcinogenesis Experiments} \end{center} \noindent In longitudinal and spatial studies, observations at a particular time or location within one subject could have complicated structures, e.g. vectors or even functions. Measurements within the same subject usually demonstrate strong correlations that are stationary in time or distance lags. The times or locations of these data being sampled may not be homogeneous. We propose a nonparametric estimator of the correlation function in such data, using kernel methods. We show that the proposed estimator has a pointwise asymptotic normal distribution, when the number of subjects is fixed and the number of vectors or functions within each subject goes to infinity. Based on the asymptotic theory, we propose a weighted block bootstrapping method in making inferences on the correlation function, where the weights account for the inhomogeneity of the distribution of the times or locations. The method is applied to a data set from a colon carcinogenesis study, in which colonic crypts were sampled from a piece of colon segment from each of the 12 rats in the experiment and the expression level of p27, an important cell cycle protein, was then measured for each cell within the sampled crypts. A simulation study is also provided to illustrate the numerical performance of the proposed method. \end{document}