Towards Early Prediction of Human iPSC Reprogramming Success

Abhineet Singh, Ila Jasra, Omar Mouhammed, Nidheesh Dadheech, Nilanjan Ray, James Shapiro
{"title":"Towards Early Prediction of Human iPSC Reprogramming Success","authors":"Abhineet Singh, Ila Jasra, Omar Mouhammed, Nidheesh Dadheech, Nilanjan Ray, James Shapiro","doi":"10.59275/j.melba.2023-3d9d","DOIUrl":null,"url":null,"abstract":"This paper presents advancements in automated early-stage prediction of the success of reprogramming human induced pluripotent stem cells (iPSCs) as a potential source for regenerative cell therapies. The minuscule success rate of iPSC-reprogramming of around 0.01% to 0.1% makes it labor-intensive, time-consuming, and exorbitantly expensive to generate a stable iPSC line since that requires culturing of millions of cells and intense biological scrutiny of multiple clones to identify a single optimal clone. The ability to reliably predict which cells are likely to establish as an optimal iPSC line at an early stage of pluripotency would therefore be ground-breaking in rendering this a practical and cost-effective approach to personalized medicine.<br>Temporal information about changes in cellular appearance over time is crucial for predicting its future growth outcomes. In order to generate this data, we first performed continuous time-lapse imaging of iPSCs in culture using an ultra-high resolution microscope. We then annotated the locations and identities of cells in late-stage images where reliable manual identification is possible. Next, we propagated these labels backwards in time using a semi-automated tracking system to obtain labels for early stages of growth. Finally, we used this data to train deep neural networks to perform automatic cell segmentation and classification.<br>Our code and data are available at <a href='https://github.com/abhineet123/ipsc_prediction'>https://github.com/abhineet123/ipsc_prediction</a>","PeriodicalId":75083,"journal":{"name":"The journal of machine learning for biomedical imaging","volume":" 1282","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The journal of machine learning for biomedical imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59275/j.melba.2023-3d9d","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

This paper presents advancements in automated early-stage prediction of the success of reprogramming human induced pluripotent stem cells (iPSCs) as a potential source for regenerative cell therapies. The minuscule success rate of iPSC-reprogramming of around 0.01% to 0.1% makes it labor-intensive, time-consuming, and exorbitantly expensive to generate a stable iPSC line since that requires culturing of millions of cells and intense biological scrutiny of multiple clones to identify a single optimal clone. The ability to reliably predict which cells are likely to establish as an optimal iPSC line at an early stage of pluripotency would therefore be ground-breaking in rendering this a practical and cost-effective approach to personalized medicine.
Temporal information about changes in cellular appearance over time is crucial for predicting its future growth outcomes. In order to generate this data, we first performed continuous time-lapse imaging of iPSCs in culture using an ultra-high resolution microscope. We then annotated the locations and identities of cells in late-stage images where reliable manual identification is possible. Next, we propagated these labels backwards in time using a semi-automated tracking system to obtain labels for early stages of growth. Finally, we used this data to train deep neural networks to perform automatic cell segmentation and classification.
Our code and data are available at https://github.com/abhineet123/ipsc_prediction
人类iPSC重编程成功的早期预测
本文介绍了人类诱导多能干细胞(iPSCs)重编程成功的自动化早期预测的进展,作为再生细胞治疗的潜在来源。iPSC重编程的极小成功率约为0.01%至0.1%,这使得生成稳定的iPSC系需要耗费大量的劳动、时间和高昂的成本,因为这需要培养数百万个细胞,并对多个克隆进行严格的生物学检查,以确定一个最佳的克隆。因此,在多能性的早期阶段,可靠地预测哪些细胞可能成为最佳的iPSC细胞系的能力将是突破性的,使其成为一种实用且具有成本效益的个性化医疗方法。关于细胞外观随时间变化的时间信息对于预测其未来的生长结果至关重要。为了获得这些数据,我们首先使用超高分辨率显微镜对培养中的iPSCs进行连续延时成像。然后,我们在后期图像中注释了细胞的位置和身份,其中可靠的手动识别是可能的。接下来,我们使用半自动跟踪系统在时间上向后传播这些标签,以获得生长早期阶段的标签。最后,我们使用这些数据来训练深度神经网络来执行自动细胞分割和分类。<br>我们的代码和数据可在<a href='https://github.com/abhineet123/ipsc_prediction'>https://github.com/abhineet123/ipsc_prediction</a>
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信