Abstract:We present an algorithm for efficient acquisition of fluorescence microscopy data sets, a problem not addressed until now in the literature. We do this as part of a larger system for protein classification based on their subcellular location patterns, and thus strive to maintain the achieved level of classification accuracy as much as possible. This problem is similar to image compression but unique due to additional restrictions, namely causality; we have access only to the information that has been scanned u… Show more
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