APEER is a free cloud-based platform to offer customizable image processing task solutions to the microscopy community. We have created modules translated from our home-built ImagingFCS_1.52 readily combined to customized your Imaging FCS workflows either for processing individual image stack or image stack in batch. The workflows runs locally somewhere and it's not shared. We believe in the spirit of open-source and therefore by making the code available as modules on the APEER platform it could help users achieving their best results. Please refer to user manual for more detail information on how to Imaging FCS on APEER,
1. FCS workflow performs autocorrelations of image stacks acquired from camera-based Fluorescence Correlation Spectroscopy (FCS). It calculate correlations, curve fitting and visualization. The module works with any 16-bit or 32-bit image stacks in any of the standard file formats: TIFF, OME-TIFF, TIF.
Sample output: interactive.html & output.xlsx
2. DC-FCCS workflow is a tool to measure molecular interactions. It is based on the the simulataneous observation of two spectrally separate fluorescence signals imaged on the two regions of the same camera. By cross-correlating the different signals of pixels at two different wavelength but corresponding to the same sample location one can determine whether the different molecules/particles interact. Analysing DC-FCCS measurements can be achieved either by Total Internal Reflection Fluorescence (TIRF) microscopy or Selective Plane Illumination Microscope (SPIM).
Sample Output: interactive.html & output.xlsx