Resumen
Assessing time-dependent changes in brain activity is of crucial importance in neuroscience. Here, we propose a novel image processing method to automatically identify active regions and assess time-dependent changes in fluorescence arising from genetically encoded indicators of activity. First, potential active regions and the corresponding active centers were extracted based on gray distance compensation. Then potential active regions were aligned through frames and, if meeting pre-determined intensity criteria, were accepted as active regions and the fluorescence changes were quantified. We validated this method with independent in vivo imaging datasets collected from transgenic mice that express the genetically encoded calcium indicator GCaMP3. Our studies indicate that the incorporation of this gray distance compensation-based algorithm substantially improves the accuracy and efficiency of detecting and quantifying cellular activity in the intact brain.