How to correct a single-cell track ---------------------------------- This guide shows you how to correct manually a single-cell track that missed detections or was truncated. Reference keys: :term:`tracking` **Prerequisite:** You have accurately segmented, and **tracked** a cell population of interest. This guide only applies to dynamic data. #. Go to the TRACK section for the cell population of interest. Click on the :icon:`eye-check,black` icon on the right side to open napari and explore tracking results. #. On the left side, click on the Image layer associated with your channel of interest. With multi-channel data, click on the :icon:`eye,black` icon to disable other Image layers. Adjust the *contrast limits* with the double slider (top left). #. Select the segmentation layer. #. Use the time axis slider below the image to find a track cut early with more detections available at later times. #. Put the slider at the last frame where the track was still uninterrupted. Pick the pipette tool (:icon:`eyedropper,black`) in the top left of part of napari. With the pipette selected, click on the mask of the cell of interest. #. Pick the Pan/Zoom button (:icon:`cursor-move`). #. Use the time axis slider to go to the next frame where a cell mask related to this track is observed. #. Double click on the cell. Say yes to the pop-up to propagate the identity of the cell from the previous frame to the current frame. If the mask is associated with another track, time propagation will be performed automatically. #. Press the *Export the modified tracks...* button to save the changes in the position table.