IMAT-ITCR Collaboration: Develop deep learning-based methods to identify subtypes of circulating tumor cells from optical microscope images
IMAT-ITCR 合作:开发基于深度学习的方法,从光学显微镜图像中识别循环肿瘤细胞的亚型
基本信息
- 批准号:10675886
- 负责人:
- 金额:$ 7.19万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-09-01 至 2023-07-31
- 项目状态:已结题
- 来源:
- 关键词:Administrative SupplementAdvanced Malignant NeoplasmAlgorithmic SoftwareAlgorithmsArchitectureArtificial IntelligenceCell modelCellsClassificationCodeCollaborationsCommunitiesComputer AssistedComputing MethodologiesConsumptionDataData AnalysesData AnalyticsData SetDevelopmentEducational CurriculumEnhancersEnvironmentEquilibriumFractionationFundingGoalsHeadHematoxylinHybridsImageImage AnalysisImage EnhancementIndividualInformaticsKnowledgeLibrariesLocationMachine LearningManualsMapsMasksMethodologyMethodsModelingMorphologic artifactsNeoplasm Circulating CellsNetwork-basedOccupationsOpticsParentsPatternPositioning AttributeProcessProtocols documentationResearchResearch PersonnelResidual stateResolutionResourcesRunningSecurityServicesSignal TransductionSoftware DesignSpeedStainsStructureSystemTechnologyTensorFlowTestingTimeTissue imagingTrainingTumor TissueUpdateVariantVertebral columnVisualizationWorkadaptation algorithmanticancer researchapplication programming interfacebasecell typecellular imagingcomputer infrastructurecomputerized data processingdeep learningdeep learning algorithmexperienceexperimental studyfluid flowfluorescence microscopegenerative adversarial networkhandheld mobile deviceimprovedinformatics toolinnovationlearning strategyloss of functionmicrochipmicroscopic imagingnoveloperationpreservationrestorationsimulationtooluser-friendlyweb services
项目摘要
IMAT-ITCR Collaboration: Develop deep learning-based methods to identify subtypes of circulating tumor
cells from optical microscope images
Project Summary/Abstract
The goal of the parent IMAT project (R21CA240185) is to develop a new platform for fractionation and profiling of CTC
subpopulations and elucidate the metastatic potential of CTCs. Currently, this work requires researchers to record hundreds
of individual microscope images of the cells captured on the microchip, integrate all images with flow fluid simulations,
and analyze three features of the capture cells (including angular position, normalized velocity and shear) for identification
of CTC subtypes. This process is very labor-intensive and time-consuming, as most of the steps rely on manual operations.
The goal of the ITCR project (1U01CA249245) is to develop an informatics platform, iSEE-Cell (image-based Spatial
pattern ExplorEr for Cells), which features a suite of informatics tools for tissue image analysis, visualization, exploration
and spatial modeling at the single-cell level. This proposed Administrative Supplement application in support of
collaboration between IMAT and ITCR-funded projects aims to develop deep learning-based methods to identify subtypes
of CTCs from optical microscope images. The rationale underlying this proposal is that the development of deep learning
methods will provide automatic characterization and classification of CTC captured on HU structured microchips. This
proposed collaborative project will leverage the technologies developed by both projects, which will bring together and
enhance the capabilities of complementary technology platforms and methodologies to advance cancer research. Innovation
of the proposed methods include the following: 1) Identification of multiple subtypes of CTCs using their location
information on an HU microchip without destructive immunostaining analysis; 2) Novel Restore-GAN model to improve
quality of microscope image obtained in CTC capture experiments and enhance predication accuracy for CTC subtypes; 3)
The proposed informatics tools will provide computer-assisted automated tools to empower CTC research with artificial
intelligence. Specific aims include: Aim 1: Using the microscope images and analysis/prediction results (from the IMAT
project) as data input to test whether algorithms to classify different types of cell from tumor tissue images (iSEE-Cell,
developed in the ICTR project) can be applied for microscope images; Aim 2: Apply novel computational methods (Restore-
GAN, developed in the ICTR project) to improve image quality of the images obtained from the IMAT project, and test
whether they can improve prediction accuracy for CTC subtypes; Aim 3: Develop a user-friendly interface to incorporate
the iSEE-Cell platform for analyzing optical/fluorescent microscope images remotely. The ability to automatically
extract/analyze information from captured cells in the microscope images is urgently needed and will dramatically enhance
the throughput and work efficiency of the IMAT project.
IMAT-ITCR协作:开发基于深度学习的方法来识别循环肿瘤的亚型
光学显微镜图像的单元格
项目摘要/摘要
父级IMAT项目(R21CA240185)的目标是开发一个新的平台,以分馏和分析CTC
亚群并阐明了CTC的转移潜力。目前,这项工作要求研究人员记录数百个
在微芯片上捕获的细胞的单个显微镜图像,将所有图像与流体模拟整合在一起,
并分析捕获单元的三个特征(包括角位置,标准化速度和剪切)以识别
CTC亚型的。由于大多数步骤都依赖手动操作,因此此过程非常耗时且耗时。
ITCR项目(1U01CA249245)的目标是开发一个信息平台,即基于图像的空间
细胞的模式探索器),该探索器具有一套用于组织图像分析,可视化,探索的信息学工具
和单细胞水平的空间建模。该提议的行政补充申请支持
IMAT和ITCR资助的项目之间的协作旨在开发基于学习的深度方法来识别亚型
来自光学显微镜图像的CTC。该提议的基本原理是深度学习的发展
方法将提供在HU结构微芯片上捕获的CTC的自动表征和分类。这
拟议的协作项目将利用这两个项目开发的技术,这些技术将汇集在一起,
增强了互补技术平台和方法论的能力,以提高癌症研究。创新
提出的方法包括以下内容:1)使用其位置识别CTC的多个亚型
有关HU微芯片的信息,而无需破坏性免疫染色分析; 2)新型的还原模型以改进
在CTC捕获实验中获得的显微镜图像的质量并提高了CTC亚型的鉴定精度; 3)
拟议的信息学工具将提供计算机辅助的自动化工具,以使CTC研究能够使用人工
智力。具体目的包括:目标1:使用显微镜图像和分析/预测结果(来自IMAT
项目)作为数据输入,以测试算法是否从肿瘤组织图像分类不同类型的细胞(ISEE-Cell,
在ICTR项目中开发的)可以用于显微镜图像;目标2:应用新颖的计算方法(还原 -
gan,在ICTR项目中开发),以提高从IMAT项目获得的图像的图像质量,并测试
它们是否可以提高CTC亚型的预测准确性;目标3:开发一个用户友好的界面以合并
ISEE细胞平台,用于远程分析光学/荧光显微镜图像。自动的能力
迫切需要从显微镜图像中捕获的细胞中提取/分析信息,并将大大增强
IMAT项目的吞吐量和工作效率。
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Deep learning detector for high precision monitoring of cell encapsulation statistics in microfluidic droplets.
- DOI:10.1039/d2lc00462c
- 发表时间:2022-10-25
- 期刊:
- 影响因子:6.1
- 作者:Gardner, Karl;Uddin, Md Mezbah;Linh Tran;Thanh Pham;Vanapalli, Siva;Li, Wei
- 通讯作者:Li, Wei
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Wei Li其他文献
Light Harvesting and Enhanced Performance of Si Quantum Dot/Si Nanowire Heterojunction Solar Cells
硅量子点/硅纳米线异质结太阳能电池的光收集和性能增强
- DOI:
10.1002/ppsc.201500192 - 发表时间:
2016-01 - 期刊:
- 影响因子:0
- 作者:
Ling Xu;Wei Li;Linwei Yu;Kunji Chen - 通讯作者:
Kunji Chen
Wei Li的其他文献
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10639274 - 财政年份:2023
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