Imaging data for NPHS2 point mutation paper w/o LAMP1

dataset.zip (29.8GB uncompressed): Raw imaris (.ims) images taken using Andor Dragonfly Spinning Disk Confocal. Organised into subfolders by subcellular stain and then order of channels. Also contains a .txt file with metadata for every image.

edited_ROIs.zip (8.46GB uncompressed): Podocyte region of interest for each image as TIFF files (.tiff), manually proofread by an expert human annotator (Aude Dorison).

imageJ_rollingball.zip (32.4GB uncompressed): Relevant channels of each raw image with background subtraction (using rolling ball method with radius of 50 pixels) processed using Fiji/ImageJ as TIFF files (.tiff). This is used for downstream processing.