Extended Data Fig. 7: 2x frame interpolation on moving lysosome of SHSY5Y cells.

2x frame interpolation of NONE, BIL, DAIN and ZS for lysosomes of SH-SY5Y cells recorded on a point-scanning confocal microscope. Overall ZS produces slightly better-quality results than DAIN even though ZS misses faster moving lysosomes which DAIN is able to capture well (example highlighted with white arrows in zoomed-in sections on the right). SSIM/RMSE/PSNR values displayed in the zoomed-in interpolated images. CAFI tools clearly outperform NONE and BIL interpolations. Scale bar: 10 μm.