Fig. 6: CAFI allows smart interpolation for a wide range of microscopy applications.

a,b, CAFI interpolation comparison of NONE, BIL, DAIN and ZS interpolation shown for D. discoideum cells (a) and fibronectin-labeled A2780 cells (b) (data from Kaukonen et al.)38, both recorded on spinning-disk confocal microscopes. c, SH-SY5Y cells recorded with a confocal brightfield microscope. d, Labeled lysosomes of SH-SY5Y cells recorded with a point-scanning confocal microscope (all scale bars, 10 μm; timestamps in top right corner of GT images); with quality metrics (SSIM/RMSE/PSNR) displayed in zoomed-in images. Arrows highlight regions of interest of visible differences between the interpolation techniques.