Computer Vision for Substrate Detection in High‐Throughput Biomaterial Screens Using Bright‐Field Microscopy

Author:

Owen Robert12ORCID,Nasir Aishah23ORCID,Amer Mahetab H.14ORCID,Nie Chenxue5,Xue Xuan16ORCID,Burroughs Laurence1ORCID,Denning Chris23ORCID,Wildman Ricky D.7ORCID,Khan Faraz A.8,Alexander Morgan R.1ORCID,Rose Felicity R. A. J.12ORCID

Affiliation:

1. School of Pharmacy Faculty of Science University of Nottingham Nottingham NG7 2RD UK

2. Biodiscovery Institute University of Nottingham Nottingham NG7 2RD UK

3. Division of Cancer & Stem Cells Faculty of Medicine & Health Sciences University of Nottingham Nottingham NG7 2RD UK

4. Division of Cell Matrix Biology and Regenerative Medicine School of Biological Sciences Faculty of Biology Medicine and Health University of Manchester Manchester M13 9NT UK

5. School of Computer Science Faculty of Science University of Nottingham Nottingham NG8 1BB UK

6. Department of Chemistry Xi'an Jiaotong‐Liverpool University Suzhou Industrial Park 215123 China

7. Centre for Additive Manufacturing Faculty of Engineering University of Nottingham Nottingham NG8 1BB UK

8. Digital and Technology Services (DTS) University of Nottingham Nottingham NG7 2RD UK

Abstract

High‐throughput screening (HTS) can be used when ab initio information is unavailable for rational design of new materials, generating data on properties such as chemistry and topography that control cell behavior. Biomaterial screens are typically fabricated as microarrays or “chips,” seeded with the cell type of interest, then phenotyped using immunocytochemistry and high‐content imaging, generating vast quantities of image data. Typically, analysis is only performed on fluorescent cell images as it is relatively simple to automate through intensity thresholding of cellular features. Automated analysis of bright‐field images is rarely performed as it presents an automation challenge as segmentation thresholds that work in all images cannot be defined. This limits the biological insight as cell response cannot be correlated to specifics of the biomaterial feature (e.g., shape, size) as these features are not visible on fluorescence images. Computer Vision aims to digitize tasks humans do by sight, such as identify objects by their shape. Herein, two case studies demonstrate how open‐source approaches, (region‐based convolutional neural network and algorithmic [OpenCV]), can be integrated into cell‐biomaterial HTS analysis to automate bright‐field segmentation across thousands of images, allowing rapid, spatial definition of biomaterial features during cell analysis for the first time.

Funder

Medical Research Council

Engineering and Physical Sciences Research Council

Publisher

Wiley

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