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FASTCOUNT Next generation stereology platform for fast, accurate 3D cell counting

FASTCOUNT Next generation stereology platform for fast, accurate 3D cell counting
FASTCOUNT 下一代体视学平台,可实现快速、准确的 3D 细胞计数
批准号:
8781853
负责人:
JACOB R GLASER
金额:
$34.81万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-11 至 2015-08-31

项目摘要

项目成果

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中文摘要
翻译
描述(由申请人提供):体视学细胞计数在过去20年中彻底改变了神经科学领域,许多研究强调了体视学细胞计数在基础神经科学和制药及生物技术研究中的影响。然而,一项研究可能需要数月时间,因为研究人员必须通过目视检查来决定是否在数千个显微镜视野内根据三维(3D)体视计数规则对每个细胞进行计数。由于这种对人工检查的依赖,体视学细胞计数仍然是非常劳动密集和耗时的。因此,更快的自动化,但不太准确的非体视细胞检测方法仍然广泛使用,尽管它们已知的缺点和偏倚的结果。为了应对这一挑战,本项目旨在开发一种用于全自动体视细胞计数的创新显微镜系统(“FASTALOTH”),建立在由我们的合作者Badri Roysam博士及其团队创建的FARSIGHT自动3D细胞检测工具包中实现的技术基础上,并将其与我们的Stereo Investigator(R)软件开发的技术相结合(在全球约1,000个实验室使用)。该项目完全符合NIMH题为“实验室到市场:大脑和行为研究工具”的计划。FASTcycle将首次允许研究人员进行自动体视学细胞计数。对神经科学研究界和整个社会的好处将是增加研究吞吐量(即,至少快10倍)在巴斯夫神经科学和制药及生物技术研究中。增加的通量将使目前由于现有方法的劳动密集型性质而不可行的新类型的研究成为可能,从而导致新的发现。我们的项目将分两个阶段实施。在第一阶段,我们将创建一个包含细胞检测、学习和编辑的原型FASTSTUNK应用程序。然后,我们将在组织切片上进行自动化3D细胞检测,用于物种,组织处理,细胞染色/标记,成像和图像预处理的各种组合。在第二阶段,我们将(i)改进和优化用于FASTRUNK的自动体视3D细胞检测算法,(ii)开发一个软件开发工具包,作为FASTRUNK和第三方软件应用程序之间的接口,以开发新的自动3D细胞检测方法,(三)开发新的图像数据管理功能,用于对最近组织清除程序处理的组织标本进行自动体视细胞计数如快速组织学,以及(iv)为快速组织学制定推荐的操作程序,解决组织制备、标记、成像和预处理问题。我们将与经验丰富的学术合作伙伴一起,在整个开发过程中对FASTRONIC进行广泛的产品验证研究,以证明其优于手动体视学细胞计数和偏倚轮廓计数。
英文摘要
DESCRIPTION (provided by applicant): Stereologic cell counting has revolutionized the field of neuroscience over the last 20 years, and numerous studies highlighting the impact of stereologic cell counting in basic neuroscience and pharmaceutical and biotechnology research continue to be published. A single study, however, may take months since investigators must decide by visual inspection whether or not to count each cell according to three-dimensional (3D) stereologic counting rules within thousands of microscopic fields-of-view. Because of this reliance on manual inspection, stereologic cell counting has remained very labor intensive and time-consuming to perform. As a result, faster automated, though less accurate non-stereologic cell detection approaches have remained in widespread use despite their known disadvantages and biased results. In response to this challenge, this project aims to develop an innovative microscope system for fully-automated stereologic cell counting ("FASTCOUNT"), building upon technology implemented in the FARSIGHT toolkit for automated 3D cell detection created by our collaborator, Dr. Badri Roysam and his team, and combining it with technology developed for our Stereo Investigator(R) software (used in approximately 1,000 laboratories worldwide). This project is fully in line with the NIMH program titled Lab to Marketplace: Tools for Brain and Behavioral Research. FASTCOUNT will allow investigators, for the first time, to perform automated stereologic cell counting. The benefit for the neuroscience research community - and society in general - will be increased research throughput (i.e., at least ten times faster) in basc neuroscience and pharmaceutical and biotechnology research. Increased throughput will make possible new kinds of studies currently not feasible due to the labor intensive nature of the existing methods, thus leading to new discoveries. Our project will be implemented in two phases. During Phase I, we will create a prototype FASTCOUNT application incorporating cell detection, learning, and editing. We will then benchmark its performance in automated 3D cell detection on tissue sections for various combinations of species, tissue processing, cell staining/labeling, imaging, and image pre-processing. During Phase II, we will (i) improve and optimize the algorithms for automated stereologic 3D cell detection used in FASTCOUNT, (ii) develop a Software Development Kit as interface between FASTCOUNT and third party software applications to allow development of new automated 3D cell detection methods, (iii) develop novel image data management functionality for automated stereologic cell counting on tissue specimens processed with recent tissue clearing procedures such as CLARITY, and (iv) develop recommended operating procedures for FASTCOUNT addressing tissue preparation, labeling, imaging, and pre-processing. Together with experienced academic collaboration partners, we will perform extensive product validation studies of FASTCOUNT throughout development to demonstrate its superiority over both manual stereologic cell counting and biased profile counting.
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