\magnification=1200 \baselineskip=20pt \nopagenumbers \font\big=cmr12 scaled \magstep2 \centerline{\bf STANFORD UNIVERSITY} \centerline{\bf DEPARTMENT OF STATISTICS} \centerline{\big DEPARTMENTAL SEMINAR} \bigskip \baselineskip=12pt \centerline{4:15 p.m., Tuesday, January 14, 2003} \centerline{Sequoia Hall Room 200} \centerline{(Cookies at 3:45 in 1st Floor Lounge)} \bigskip \baselineskip=15pt \centerline{\sl Jun S. Liu} \centerline{\sl Department of Statistics} \centerline{\sl Harvard University} \bigskip \centerline{\bf Towards the Integration of Sequence Motif Discovery and Microarray Analysis} \bigskip Although numerous approaches for using microarray data to help finding DNA regulatory binding motifs have been proposed in the past years, available methods either require examining too many motifs, which results in possibly many false positive results, or use motif-finding methods without adequate specificity to determine significant motifs. We developed a new method Motif Regressor for alleviating some of the shortcomings of existing methods. Our method makes use of a newly developed motif finding approach MDscan to provide a set of candidate regulatory motifs in the upstreams of genes that are most overexpressed (or underexpressed) in an experimental condition (or cluster). These putative motifs are re-examined with a regression analysis to further utilize the microarray information. I will illustrate the application of this method on several yeast microarray experiments. I will also discuss some issues related to the motif analysis such as motif clustering, database motif search, etc. \bye