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More about Genetic Models of Disease Research Program Computational Microscopy Laboratory
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Research Interests The recently-developed structured-illumination microscope provides depth resolution comparable to that of a confocal microscope. I developed and tested an image estimation method that greatly improves the image resolution of this microscope (Conchello, 2005). Existing deconvolution methods assume that imaging conditions do not vary as a through-focus stack is recorded. However, for many thick biological specimens, this does not hold. An exact formulation for this process, although possible, requires large amounts of computer memory and very long computation times. We recently developed a method that incorporates approximations to the process of image formation and makes computer time and memory requirements practical (Preza and Conchello, 2004). Current methods also require precise information on imaging conditions, including the refractive index and thickness of all material between the objective and the specimen. We developed a method to estimate these parameters while out-of-focus light is being removed (Markham and Conchello, 1999). We are modifying our method to estimate only the few imaging parameters that are usually unknown. This will greatly reduce computation time and make use of the algorithm more practical. To make the algorithms available and easy to use, we are closely collaborating with Dr. Mike Dresser to develop OMRFCOSM, a software package for computational microscopy that will include several methods for deconvolution, as well as tools for image correction, visualization and analysis. Joined OMRF Scientific Staff in 2003. Mailing Address
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