Abstract:Temporal, multimodal microscopy imaging of live cells is becoming widely used in studies of cellular processes. In general, temporal sequences of images with functional and morphological data from live cells are acquired using multiple image sensors. The images from the different sources usually differ in resolution and have non-coincident fields of view, making the merging process complex. We present a new tool – iCellFusion – that performs data fusion of images from Phase-Contrast Microscopy and Fluorescence… Show more
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