Cell segmentation — epitools.analysis.segmentation
#
This module contains functions for segmenting 3D (ZYX) and 4D (TZXY) images.
- epitools.analysis.segmentation.calculate_segmentation(projection, spot_sigma, outline_sigma, threshold)#
Segment an image using a thresholded local-minima-seeded watershed algorith.
This will segment cells in images with marked membranes that have a high signal intensity.
The two sigma parameters allow tuning the segmentation result. Under the hood, this algorithm first applies two Gaussian blurs, then uses a local minima detection and seeded watershed. Afterwards, all objects are removed that have an average intensity below a given threshold.
- Parameters
projection (numpy.ndarray[Any, numpy.dtype[numpy.float64]]) – A projected image stack processed using Epitools.
spot_sigma (float) – Controls how close segmented cells can be - larger values result in more seeds used in the segmentation
outline_sigma (float) – Controls how precisely segmented cells are outlined - larger values result in more precise (rougher) cell boundaries.
threshold (float) – Cells with an average intensity below threshold are will be removed from the segmentation and treated as background.
- Returns
- np.NDArray
Seeds used in the segmentated
- np.NDArray
Labels of the segmented image (0 corresponds to background)
- Return type
tuple[numpy.ndarray[Any, numpy.dtype[numpy.float64]], numpy.ndarray[Any, numpy.dtype[numpy.int64]]]