cellstitch-cuda 1.2.3

CUDA-accelerated CellStitch 3D labeling using Instanseg segmentation.

CellStitch-Cuda: CUDA-accelerated CellStitch 3D labeling.

About this repo

An overhaul of the CellStitch algorithm, developed by Yining Liu and Yinuo Jin (original repository), publication can be found here.

Some major adjustments:

• Replaced NumPy with CuPy for GPU-accelerated calculations.
• Replaced nested for-loops with vectorized calculations for dramatic speedups (~100x).
• Included novel segmentation method InstanSeg, which enables multichannel inputs (repo and publication).
• An all-in-one method that takes an ZCYX-formatted .tif file, performs the correct transposes, and writes stitched labels.
• Included a histogram-based bleach correction to adjust for signal degradation over the Z-axis (originally developed for ImageJ in (Miura 2020) and released for Python by marx-alex in napari-bleach-correct).

Some comparisons

The calculations were run on the same machine (GPU: NVIDIA Quadro RTX 6000 24 GB; CPU: Intel Xeon Gold 6252 (48/96 cores); RAM: 1024 GB), the core count of which gave it a clear parallel-processing advantage. This particularly affects the fill_holes_and_remove_small_masks function, which has been rewritten to utilize parallel processing.

In image A, GPU VRAM load was ~200 MB at its peak.

In image B, GPU VRAM load was ~2442 MB at its peak

Installation

Notes

This setup has so far only been verified on Windows-based, CUDA-accelerated machines. Testing has only been performed on CUDA 12.x. There are no reasons why 11.x should not work (check instructions), but your mileage may vary.

Conda setup

conda create -n cellstitch-cuda python=3.11
conda activate cellstitch-cuda

Install using PyPi

pip install cellstitch-cuda
pip uninstall torch
conda install pytorch pytorch-cuda=12.4 -c conda-forge -c pytorch -c nvidia

You may replace the version number for pytorch-cuda with whatever is applicable for you.

Additional steps for CUDA 11.x

pip uninstall cupy-cuda12x
pip install cupy-cuda11x

Instructions

Example code

For more detail, see examples/.

From an image

This assumes a multichannel grayscale image in the order ZCYX. Single-channel images are currently not supported, but will be in the future.

from cellstitch_cuda.pipeline import cellstitch_cuda

img = "path/to/image.tif"  # ZCYX
# or feed img as a numpy ndarray

volumetric_masks = cellstitch_cuda(img)

From pre-existing orthogonal labels

These are label images over the Z-, X, and Y-axis. They are assumed to be in the order ZYX. If you set output_masks=True in the cellstitch_cuda()-function, these masks will be written to disk (either in the input folder, or in the folder set in output_path).

from cellstitch_cuda.pipeline import full_stitch
import tifffile

# Define xy_masks, yz_masks, xz_masks
yx_masks = tifffile.imread("path/to/yx_masks.tif")  # ZYX
yz_masks = tifffile.imread("path/to/yz_masks.tif")  # ZYX
xz_masks = tifffile.imread("path/to/xz_masks.tif")  # ZYX

volumetric_masks = full_stitch(yx_masks, yz_masks, xz_masks)

Arguments

cellstitch_cuda.pipeline.cellstitch_cuda()

cellstitch_cuda() takes the following arguments:

• img: Either a path pointing to an existing image, or a numpy.ndarray. Must be 4D (ZCYX).
• output_masks: True to write all masks to the output path, or False to only return the final stitched mask. Default False
• output_path: Set to None to write to the input file location (if provided). Ignored of output_masks is False. Default None
• seg_mode: Instanseg segmentation mode: "nuclei" to only return nuclear masks, "cells" to return all the cell masks (including those without nuclei), or "nuclei_cells", which returns only cells with detected nuclei. Default "nuclei_cells"
• pixel_size: XY pixel size in microns per pixel. When set to None, will be read from img metadata if possible. Default None
• z_step: Z pixel size (z step) in microns per step. When set to None, will be read from img metadata if possible. Default None
• bleach_correct: Whether histogram-based signal degradation correction should be applied to img. Default True
• filtering: Whether the fill_holes_and_remove_small_masks function should be executed. With larger datasets, this has the tendency to massively slow down the postprocessing. Default True
• n_jobs: Set the number of threads to be used in parallel processing tasks. Use 1 for debugging. Generally, best left at the default value. Default -1
• verbose: Verbosity. Default False

cellstitch_cuda.pipeline.full_stitch()

full_stitch() takes the following arguments:

• xy_masks_prior: numpy.ndarray with XY masks, order ZYX
• yz_masks: numpy.ndarray with YZ masks, order ZYX
• xz_masks: numpy.ndarray with XZ masks, order ZYX
• nuclei: numpy.ndarray with XY masks of nuclei, order ZYX. If provided, it will run the function filter_nuclei_cells() to filter volumetric masks by the presence of a 2D nucleus mask. Default None
• filter: Use CellPose-based fill_holes_and_remove_small_masks() function. Default True
• n_jobs: Number of threads used. Set n_jobs to 1 for debugging parallel processing tasks. Default -1
• verbose: Verbosity. Default False

References

Goldsborough, T., O’Callaghan, A., Inglis, F., Leplat, L., Filbey, A., Bilen, H., & Bankhead, P. (2024) A novel channel invariant architecture for the segmentation of cells and nuclei in multiplexed images using InstanSeg. bioRxiv, 2024.09.04.611150. doi: 10.1101/2024.09.04.611150

Liu, Y., Jin, Y., Azizi, E., & Blumberg, E. (2023) Cellstitch: 3D cellular anisotropic image segmentation via optimal transport. BMC Bioinformatics, 24(480). doi: 10.1186/s12859-023-05608-2

Miura, K. (2020) Bleach correction ImageJ plugin for compensating the photobleaching of time-lapse sequences. F1000Res, 9:1494. doi: 10.12688/f1000research.27171.1

Stringer, C., Wang, T., Michaelos, M., & Pachitariu, M. (2021) Cellpose: a generalist algorithm for cellular segmentation. Nature Methods, 18(1), 100-106. doi: 10.1038/s41592-020-01018-x