3-D Image Restoration for Polarized Light Microscopy
偏光显微镜的 3D 图像恢复
基本信息
- 批准号:6656953
- 负责人:
- 金额:$ 25.29万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-09-15 至 2004-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): We have been developing and applying a new
type of polarized light microscope (the P01-Scope) which dramatically enhances
the analytic power of the traditional polarizing microscope. The P01-Scope
incorporates a universal compensator, made from computer driven liquid crystal
devices, to measure the birefringent fine structure at high sensitivity (0.02
nm birefringence retardation), high resolution (0.2 pm), simultaneously over
the whole field of view, and for all orientations of the birefringence axis
within the focus plane. A 3-dimensional birefringent specimen, such as a living
cell, is imaged with the Pol-Scope as a series of optical Sections. Each
section contains the birefringence of in-focus structures, such as membranous
stacks, aligned filament arrays and individual filament bundles. However, the
measurements of in-focus birefringences have spurious contributions from out-of
focus cellular components. The structural analysis of the detailed and
quantitative information afforded by the P01-Scope is often limited because of
these spurious birefringence contributions. Therefore, to take full advantage
of the quantitative Pol-Scope images, the out-of-focus information needs to be
identified and removed. We are proposing to develop a computational restoration
procedure to remove the effect of out-of-focus components on the measurements
of in-focus birefringences. The P01-Scope restoration algorithm will be based
on procedures established for fluorescence microscopy that we will modify to
account for the specific properties of partial coherent imaging with polarized
light. The first development goal is to establish a forward procedure that is
used to compute image features based on measured point spread functions and
known or estimated positions, magnitudes and axis orientations of birefringent
objects. The second goal is to find the inverse procedure that optimizes a
numerical estimate of object birefringences in volume elements that are
contained in P01-Scope optical sections. The inverse procedure iteratively
minimizes the difference between experimental and computed images. This process
ends in a stable 3-D distribution of positions, magnitudes and axis
orientations of specimen birefringences. The image restoration procedures will
greatly enhance the utility of the P01-Scope for biological and medical
applications to non-invasively analyze the architectural dynamics of living
cells.
描述(由申请人提供):我们一直在开发和应用新的
极化光学显微镜(P01-SCOPE)的类型,可显着增强
传统偏振显微镜的分析能力。 P01-SCOPE
结合了由计算机驱动液晶制成的通用补偿器
设备,以高灵敏度测量双折射良好结构(0.02
NM双重智障),高分辨率(0.2 pm),同时超过
整个视野,以及双方轴的所有方向
在聚焦平面内。一个三维的双折射标本,例如居住
细胞与波波式成像为一系列光学截面。每个
部分包含聚焦结构的双折射,例如膜
堆栈,对齐的灯丝阵列和单个灯丝束。但是,
对重点双折射的测量结果有虚假的贡献
聚焦细胞成分。详细的结构分析
P01-SCOPE提供的定量信息通常受到限制
这些虚假的双折射贡献。因此,充分利用
在定量的pol-scope图像中,需要进行异位信息
确定并删除。我们建议开发计算恢复
删除焦点组件对测量的效果的程序
焦点双折射。 P01-Scope Restoration算法将基于
根据荧光显微镜确定的程序,我们将修改为
考虑与极化的部分相干成像的特定特性
光。第一个发展目标是建立一个远期程序
用于根据测量点扩展功能计算图像特征和
双折射的已知或估计位置,大小和轴向取向
对象。第二个目标是找到优化一个的逆过程
卷元素中对象双折射的数值估计
包含在P01-Scope光学部分中。反向过程迭代
最小化实验图像和计算图像之间的差异。这个过程
以稳定的位置,幅度和轴的稳定3-D分布结束
标本双向框的方向。图像修复程序将
极大地增强了P01-SCOPE的生物学和医疗效用
非侵入性分析生活的建筑动力学的应用
细胞。
项目成果
期刊论文数量(5)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Polarized light microscopy in reproductive and developmental biology.
- DOI:10.1002/mrd.22221
- 发表时间:2015-07
- 期刊:
- 影响因子:2.5
- 作者:Koike-Tani M;Tani T;Mehta SB;Verma A;Oldenbourg R
- 通讯作者:Oldenbourg R
pH dependent isotropic to nematic phase transitions in graphene oxide dispersions reveal droplet liquid crystalline phases.
- DOI:10.1039/c4cc00970c
- 发表时间:2014-05
- 期刊:
- 影响因子:4.9
- 作者:Rachel Tkacz;R. Oldenbourg;Shalin B. Mehta;Morteza Miansari;Amitabh Verma;M. Majumder
- 通讯作者:Rachel Tkacz;R. Oldenbourg;Shalin B. Mehta;Morteza Miansari;Amitabh Verma;M. Majumder
Polarized light microscopy: principles and practice.
偏光显微镜:原理与实践。
- DOI:10.1101/pdb.top078600
- 发表时间:2013
- 期刊:
- 影响因子:0
- 作者:Oldenbourg,Rudolf
- 通讯作者:Oldenbourg,Rudolf
Pac-man motility of kinetochores unleashed by laser microsurgery.
激光显微手术释放动粒的吃豆人运动。
- DOI:10.1091/mbc.e12-04-0314
- 发表时间:2012
- 期刊:
- 影响因子:3.3
- 作者:LaFountainJr,JamesR;Cohan,ChristopherS;Oldenbourg,Rudolf
- 通讯作者:Oldenbourg,Rudolf
Kinetochore-driven outgrowth of microtubules is a central contributor to kinetochore fiber maturation in crane-fly spermatocytes.
着丝粒驱动的微管生长是鹤蝇精母细胞着丝粒纤维成熟的主要贡献者。
- DOI:10.1091/mbc.e14-01-0008
- 发表时间:2014
- 期刊:
- 影响因子:3.3
- 作者:LaFountainJr,JamesR;Oldenbourg,Rudolf
- 通讯作者:Oldenbourg,Rudolf
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RUDOLF OLDENBOURG其他文献
RUDOLF OLDENBOURG的其他文献
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{{ truncateString('RUDOLF OLDENBOURG', 18)}}的其他基金
3D imaging of cells and tissues using polarized light microscopy
使用偏光显微镜对细胞和组织进行 3D 成像
- 批准号:
10381555 - 财政年份:2019
- 资助金额:
$ 25.29万 - 项目类别:
3D imaging of cells and tissues using polarized light microscopy
使用偏光显微镜对细胞和组织进行 3D 成像
- 批准号:
10597635 - 财政年份:2019
- 资助金额:
$ 25.29万 - 项目类别:
Instantaneous 3D imaging of cells and tissues using polarized light microscopy
使用偏光显微镜对细胞和组织进行瞬时 3D 成像
- 批准号:
9527370 - 财政年份:2015
- 资助金额:
$ 25.29万 - 项目类别:
Instantaneous 3D imaging of cells and tissues using polarized light microscopy
使用偏光显微镜对细胞和组织进行瞬时 3D 成像
- 批准号:
8863961 - 财政年份:2015
- 资助金额:
$ 25.29万 - 项目类别:
3-D Image Restoration for Polarized Light Microscopy
偏光显微镜的 3D 图像恢复
- 批准号:
6400765 - 财政年份:2001
- 资助金额:
$ 25.29万 - 项目类别:
3-D Image Restoration for Polarized Light Microscopy
偏光显微镜的 3D 图像恢复
- 批准号:
6526004 - 财政年份:2001
- 资助金额:
$ 25.29万 - 项目类别:
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3-D Image Restoration for Polarized Light Microscopy
偏光显微镜的 3D 图像恢复
- 批准号:
6400765 - 财政年份:2001
- 资助金额:
$ 25.29万 - 项目类别:
3-D Image Restoration for Polarized Light Microscopy
偏光显微镜的 3D 图像恢复
- 批准号:
6526004 - 财政年份:2001
- 资助金额:
$ 25.29万 - 项目类别: