Genomic and Bioinformatic Analysis of Genetic Regulatory Networks

Barak A. Cohen, Ph.D.

DEPARTMENT OF Genetics
Keywords: genome analysis, cell cycle, bioinformatics, gene expression

Most variation in the human population, including the susceptibilty to diseases, is quantitative and genetically complex. Despite the primary importance of quanitative variation in medicine, the genetic basis of quantitative traits is poorly understaood at the molecular level. Using yeast as a model system we are unraveling the molecular basis of naturally occurring phenotypic variation. We have assembled a collection of natural isolates of S. cerevisiae that show many phenotypic differences. Using a combination of modern functional genomics and classical quantitative genetics we intend to quantify the relative contribution of coding versus non-coding polymorphism to this natural variation. We are also investigating the role that variation in gene expression plays in generating this phenotypic diversity.

A second focus of the lab is to gain the ability to predict the expression pattern of a gene based on the sequence of its promoter. To this end we are developing new technologies to assay large numbers of engineered promoters with different combinations of cis-regulatory sites. Simultaneously we are developing a quantitative framework to use this data to predict the expression patterns both of promoters in the genome and of novel, engineered promoters.

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