Quantifying morphologies of developing neuronal cells using deep learning with imperfect annotations

IF 2.9 Q3 NEUROSCIENCES IBRO Neuroscience Reports Pub Date : 2023-12-30 DOI:10.1016/j.ibneur.2023.12.009
Amir Masoud Nourollah , Hamid Hassanpour , Amin Zehtabian
{"title":"Quantifying morphologies of developing neuronal cells using deep learning with imperfect annotations","authors":"Amir Masoud Nourollah ,&nbsp;Hamid Hassanpour ,&nbsp;Amin Zehtabian","doi":"10.1016/j.ibneur.2023.12.009","DOIUrl":null,"url":null,"abstract":"<div><p>The functionality of human intelligence relies on the interaction and health of neurons, hence, quantifying neuronal morphologies can be crucial for investigating the functionality of the human brain. This paper proposes a deep learning (DL) based method for segmenting and quantifying neuronal structures in fluorescence microscopy images of developing neuronal cells cultured in vitro. Compared to the majority of supervised DL-based segmentation methods that heavily rely on creating exact corresponding masks of neuronal structures for the preparation of training samples, the proposed approach allows for imperfect annotation of neurons, as it only requires tracing the centrelines of the neurites. This ability accelerates the preparation of training data by several folds. Our proposed framework is built on a modified version of PSPNet with an EfficientNet backbone pre-trained on the CityScapes dataset. To handle the imperfectness of training samples, we incorporated a weighted combination of two loss functions, namely the Dice loss and Lovász loss functions, into our network. We evaluated the proposed framework and several other state-of-the-art methods on a published dataset of approximately 900 manually quantified cultured mouse neurons. Our results indicate a close correlation between the proposed method and manual quantification in terms of neuron length and the number of branches while demonstrating improved analysis speed. Furthermore, the proposed method achieved high accuracy in neuron segmentation, as evidenced by the evaluation of the neurons’ length and number of branches.</p></div>","PeriodicalId":13195,"journal":{"name":"IBRO Neuroscience Reports","volume":"16 ","pages":"Pages 118-126"},"PeriodicalIF":2.9000,"publicationDate":"2023-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667242123022959/pdfft?md5=5c07bfacaa94592064f32ac9ed611674&pid=1-s2.0-S2667242123022959-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IBRO Neuroscience Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667242123022959","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

The functionality of human intelligence relies on the interaction and health of neurons, hence, quantifying neuronal morphologies can be crucial for investigating the functionality of the human brain. This paper proposes a deep learning (DL) based method for segmenting and quantifying neuronal structures in fluorescence microscopy images of developing neuronal cells cultured in vitro. Compared to the majority of supervised DL-based segmentation methods that heavily rely on creating exact corresponding masks of neuronal structures for the preparation of training samples, the proposed approach allows for imperfect annotation of neurons, as it only requires tracing the centrelines of the neurites. This ability accelerates the preparation of training data by several folds. Our proposed framework is built on a modified version of PSPNet with an EfficientNet backbone pre-trained on the CityScapes dataset. To handle the imperfectness of training samples, we incorporated a weighted combination of two loss functions, namely the Dice loss and Lovász loss functions, into our network. We evaluated the proposed framework and several other state-of-the-art methods on a published dataset of approximately 900 manually quantified cultured mouse neurons. Our results indicate a close correlation between the proposed method and manual quantification in terms of neuron length and the number of branches while demonstrating improved analysis speed. Furthermore, the proposed method achieved high accuracy in neuron segmentation, as evidenced by the evaluation of the neurons’ length and number of branches.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用不完善注释的深度学习量化发育中神经元细胞的形态
人类智能的功能依赖于神经元的相互作用和健康,因此,量化神经元形态对于研究人类大脑的功能至关重要。本文提出了一种基于深度学习(DL)的方法,用于分割和量化体外培养的发育中神经元细胞荧光显微镜图像中的神经元结构。大多数基于深度学习的监督分割方法都严重依赖于创建神经元结构的精确对应掩模来准备训练样本,与之相比,本文提出的方法允许对神经元进行不完全标注,因为它只需要追踪神经元的中心线。这种能力可将训练数据的准备工作加快数倍。我们提出的框架是建立在经过修改的 PSPNet 基础上的,其骨干是在 CityScapes 数据集上预先训练过的 EfficientNet。为了处理训练样本的不完美性,我们在网络中加入了两个损失函数的加权组合,即 Dice 损失函数和 Lovász 损失函数。我们在一个已发布的数据集上对所提出的框架和其他几种最先进的方法进行了评估,该数据集包含约 900 个人工量化培养的小鼠神经元。我们的结果表明,在神经元长度和分支数量方面,所提出的方法与人工量化方法之间具有密切的相关性,同时还提高了分析速度。此外,通过对神经元长度和分支数量的评估,我们提出的方法在神经元分割方面达到了很高的准确度。
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 去求助
来源期刊
IBRO Neuroscience Reports
IBRO Neuroscience Reports Neuroscience-Neuroscience (all)
CiteScore
2.80
自引率
0.00%
发文量
99
审稿时长
14 weeks
期刊介绍:
期刊最新文献
Endurance training mitigates obesity-induced hippocampal impairment by enhancing neurotrophin signalling, synaptic plasticity, and cellular responses in a female rat model Structural remodeling of medium spiny neurons in the tail of the striatum and stress-related behavioral alterations after early handling and adolescent stress in male rats Norepinephrine and dopamine Imbalance in the medial frontal gyrus from patients with Alzheimer's disease Case report of stiff - person syndrome and literature review Real-time autonomic responses to insulin-induced hypoglycaemia in volunteers with type I diabetes compared to controls
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1