Systematic evaluation of deep learning design choices for image-based organ-on-chip quality assessment.

IF 6.3 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2026-10-27 DOI:10.1039/d6lc00731g
Ayse B Oktay, Arpit Tandon, Brian E Howard, Ruchir R Shah
{"title":"Systematic evaluation of deep learning design choices for image-based organ-on-chip quality assessment.","authors":"Ayse B Oktay, Arpit Tandon, Brian E Howard, Ruchir R Shah","doi":"10.1039/d6lc00731g","DOIUrl":null,"url":null,"abstract":"<p><p>Label-free brightfield microscopy is widely used to monitor organ-on-chip (OOC) cultures, but manual quality assessment can be subjective, labor-intensive, and difficult to standardize across biological conditions. Using a public dataset of 3072 microscopy images from six cell lines, we systematically evaluated four questions relevant to automated OOC quality assessment: (1) how model architecture and image resolution affect performance, (2) whether predictive information is localized or distributed across the image, (3) whether biological metadata provides complementary information beyond the image, and (4) how well learned quality representations transfer across cell lines. We found that (1) both architecture and input resolution influenced performance, with increasing resolution from 224 × 224 to 768 × 768 improving ConvNeXt-Tiny accuracy from 0.852 to 0.910 and improving performance for five of six evaluated convolutional neural networks (CNNs); (2) multiple instance learning and saliency analyses indicated that quality relevant information was distributed across multiple image regions rather than dominated by isolated local defects; (3) biological metadata provided only modest additional benefit, with the best metadata-conditioned model achieving an accuracy of 0.915 compared with 0.910 for image-only classification; and (4) transfer to previously unseen cell lines varied substantially (ROC-AUC 0.783-0.999), while finetuning models with target-cell-line data substantially recovered performance, increasing pooled accuracy from 0.791 to 0.890. Domain-adversarial training did not consistently improve transfer. Rather than introducing a new deep learning architecture, the novelty of this work lies in systematically evaluating these OOC-specific design and generalization factors within a common framework. These findings highlight image resolution, biological-domain validation, and target-domain adaptation as important considerations for robust automated OOC quality assessment.</p>","PeriodicalId":85,"journal":{"name":"Lab on a Chip","volume":" ","pages":"5805-5823"},"PeriodicalIF":6.3000,"publicationDate":"2026-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lab on a Chip","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1039/d6lc00731g","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Label-free brightfield microscopy is widely used to monitor organ-on-chip (OOC) cultures, but manual quality assessment can be subjective, labor-intensive, and difficult to standardize across biological conditions. Using a public dataset of 3072 microscopy images from six cell lines, we systematically evaluated four questions relevant to automated OOC quality assessment: (1) how model architecture and image resolution affect performance, (2) whether predictive information is localized or distributed across the image, (3) whether biological metadata provides complementary information beyond the image, and (4) how well learned quality representations transfer across cell lines. We found that (1) both architecture and input resolution influenced performance, with increasing resolution from 224 × 224 to 768 × 768 improving ConvNeXt-Tiny accuracy from 0.852 to 0.910 and improving performance for five of six evaluated convolutional neural networks (CNNs); (2) multiple instance learning and saliency analyses indicated that quality relevant information was distributed across multiple image regions rather than dominated by isolated local defects; (3) biological metadata provided only modest additional benefit, with the best metadata-conditioned model achieving an accuracy of 0.915 compared with 0.910 for image-only classification; and (4) transfer to previously unseen cell lines varied substantially (ROC-AUC 0.783-0.999), while finetuning models with target-cell-line data substantially recovered performance, increasing pooled accuracy from 0.791 to 0.890. Domain-adversarial training did not consistently improve transfer. Rather than introducing a new deep learning architecture, the novelty of this work lies in systematically evaluating these OOC-specific design and generalization factors within a common framework. These findings highlight image resolution, biological-domain validation, and target-domain adaptation as important considerations for robust automated OOC quality assessment.

基于图像的片上器官质量评估中深度学习设计选择的系统评价。
无标签明场显微镜被广泛用于监测器官芯片(OOC)培养,但人工质量评估可能是主观的,劳动密集型的,并且难以在生物条件下标准化。使用来自6个细胞系的3072张显微镜图像的公共数据集,我们系统地评估了与自动化OOC质量评估相关的四个问题:(1)模型架构和图像分辨率如何影响性能;(2)预测信息是局部的还是分布在整个图像中;(3)生物元数据是否提供了图像之外的补充信息;(4)良好的学习质量表征如何在细胞系之间传递。我们发现(1)结构和输入分辨率都会影响性能,将分辨率从224 × 224增加到768 × 768,将ConvNeXt-Tiny的精度从0.852提高到0.910,并提高了六个评估的卷积神经网络(cnn)中的五个的性能;(2)多实例学习和显著性分析表明,质量相关信息分布在多个图像区域,而不是由孤立的局部缺陷主导;(3)生物元数据仅提供适度的额外效益,最佳元数据条件模型的分类准确率为0.915,而仅图像分类的分类准确率为0.910;(4)转移到以前未见过的细胞系上的差异很大(ROC-AUC 0.783-0.999),而使用目标细胞系数据进行微调的模型基本上恢复了性能,将池精度从0.791提高到0.890。领域对抗训练并不能持续改善迁移。这项工作的新颖之处在于在一个共同的框架内系统地评估这些面向对象的特定设计和泛化因素,而不是引入一个新的深度学习架构。这些发现强调了图像分辨率、生物域验证和目标域自适应是健壮的自动化OOC质量评估的重要考虑因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书