Fig. 8
From: Enhancing image resolution of confocal fluorescence microscopy with deep learning
Super-resolution imaging of live-cell microtubules using TCAN. (a) The super-resolved output image of live-cell microtubules. Bottom right: a fraction of the corresponding STED image (Leica TCS SP8 STED confocal microscope) used as comparison. Scale bar, 3 μm. (b), (d) Time-lapse STED images at four time points are shown at a magnified scale. (c, e) Time-lapse network output images at four time points are shown at a magnified scale. Scale bar, 1 μm. (f) A diffraction-limited confocal microscopy images (Nikon A1R MP+ microscope) used as input to the network. (g) The super-resolved output image of live-cell microtubules. Scale bar, 3 μm. (h, j) Time-lapse confocal images at five time points are shown at a magnified scale. (i, k) Time-lapse network output images at five time points are shown at a magnified scale. Scale bar, 0.5 μm