Share Email Print
cover

Proceedings Paper

Improved automated segmentation of human kidney organoids using deep convolutional neural networks
Author(s): Michael MacDonald; Theron R. Fennel; Asha Singanamalli; Nelly M. Cruz; Mohammad Yousefhussein; Yousef Al-Kofahi; Benjamin S. Freedman
Format Member Price Non-Member Price
PDF $17.00 $21.00

Paper Abstract

Organoids are multicellular structures grown in the lab that resemble tissues or organs of the body. We recently generated human kidney organoids compatible with high throughput screening for developmental and disease phenotypes. Accurately segmenting large-scale image collections of organoids remains a challenge. We investigated automated segmentation of these structures using both conventional image processing algorithms and two different deep convolutional neural network architectures. Our dataset consisted of multi-channel images of organoids in 384-well plates, labeling distal tubules, proximal tubules, and podocytes as distinct segments. These images were used either for training and validation, or for testing. Each image was initially subjected to automated segmentation using a customized CellProfiler workflow. Separately, we performed semantic organoid segmentation using a Residual UNet (ResUNet) architecture, and instance organoid segmentation using a Mask R-CNN (MRCNN) architecture. For the latter, we compared model performance after initializing network weights in three different ways: randomly, using ResNet-50 weights pre-trained on the COCO dataset, and using ResUNet weights pre-trained on organoid images. Using ResUNet or randomly initializing MRCNN backbone weights provided improved semantic segmentation compared to using precomputed weights from COCO or ResUNet, or to using the CellProfiler workflow. Conversely, using precomputed weights to initialize MRCNN provided better instance segmentation accuracy and sensitivity than random initialization. Our findings provide a basis for automated segmentation of organoids with convolutional neural networks, to aid in high throughput screening for compounds relevant to renal phenotypes.

Paper Details

Date Published: 10 March 2020
PDF: 8 pages
Proc. SPIE 11313, Medical Imaging 2020: Image Processing, 113133B (10 March 2020); doi: 10.1117/12.2549830
Show Author Affiliations
Michael MacDonald, GE Research (United States)
Theron R. Fennel, Univ. of Washington School of Medicine (United States)
Asha Singanamalli, GE Research (United States)
Nelly M. Cruz, Univ. of Washington School of Medicine (United States)
Mohammad Yousefhussein, GE Research (United States)
Yousef Al-Kofahi, GE Research (United States)
Benjamin S. Freedman, Univ. of Washington School of Medicine (United States)


Published in SPIE Proceedings Vol. 11313:
Medical Imaging 2020: Image Processing
Ivana Išgum; Bennett A. Landman, Editor(s)

© SPIE. Terms of Use
Back to Top
PREMIUM CONTENT
Sign in to read the full article
Create a free SPIE account to get access to
premium articles and original research
Forgot your username?
close_icon_gray