TY - JOUR
T1 - Computer Vision for Substrate Detection in High-Throughput Biomaterial Screens Using Bright-Field Microscopy
AU - Owen, Robert
AU - Nasir, Aishah
AU - Amer, Mahetab H.
AU - Nie, Chenxue
AU - Xue, Xuan
AU - Burroughs, Laurence
AU - Denning, Chris
AU - Wildman, Ricky D.
AU - Khan, Faraz A.
AU - Alexander, Morgan R.
AU - Rose, Felicity R.A.J.
N1 - Publisher Copyright:
© 2024 The Author(s). Advanced Intelligent Systems published by Wiley-VCH GmbH.
PY - 2024/8/22
Y1 - 2024/8/22
N2 - 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.
AB - 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.
KW - CellProfiler
KW - detectron2
KW - feature identification
KW - image analysis
KW - machine learning
KW - polymer microarray
KW - TopoChip
UR - https://onlinelibrary.wiley.com/doi/full/10.1002/aisy.202400573
UR - http://www.scopus.com/inward/record.url?scp=85201607709&partnerID=8YFLogxK
U2 - 10.1002/aisy.202400573
DO - 10.1002/aisy.202400573
M3 - Article
AN - SCOPUS:85201607709
SN - 2640-4567
JO - Advanced Intelligent Systems
JF - Advanced Intelligent Systems
ER -