Andrew Sundstrom, Silvio Cirrone, Salvatore Paxia, Carlin Hsueh, Rachel Kjolby, James K Gimzewski, Jason Reed, Bud Mishra
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We are motivated by an application of atomic force microscopy (AFM) image processing needed to solve a central problem in molecular biology, aimed at obtaining the complete transcription profile of a single cell, a snapshot that shows which genes are being expressed and to what degree. Reed et al (Single molecule transcription profiling with AFM, Nanotechnology, 18:4, 2007) showed the transcription profiling problem reduces to making high-precision measurements of biomolecule backbone lengths, correct to within 20-25 bp (6-7.5 nm). Here we present an image processing and length estimation pipeline using AFM that comes close to achieving these measurement tolerances. In particular, we develop a biased length estimator on trained coefficients of a simple linear regression model, biweighted by a Beaton-Tukey function, whose feature universe is constrained by James-Stein shrinkage to avoid overfitting. 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Often the relevant features of a particular pattern analysis problem are easy to enumerate, as when statistical structures of the patterns are well understood from the knowledge of the domain. We study a problem from molecular image analysis, where such a domain-dependent understanding may be lacking to some degree and the features must be inferred via machine-learning techniques. In this paper, we propose a rigorous, fully-automated technique for this problem. We are motivated by an application of atomic force microscopy (AFM) image processing needed to solve a central problem in molecular biology, aimed at obtaining the complete transcription profile of a single cell, a snapshot that shows which genes are being expressed and to what degree. 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引用次数: 12
摘要
在模式分析中有许多问题的例子,如果图像的少量有用的特征或参数是先验的,或者可以很好地估计,那么通常有可能获得系统的特征。当从领域的知识中很好地理解模式的统计结构时,通常很容易列举特定模式分析问题的相关特征。我们研究了一个来自分子图像分析的问题,其中可能在某种程度上缺乏这种依赖于领域的理解,并且必须通过机器学习技术推断特征。在本文中,我们提出了一种严格的、全自动的技术来解决这个问题。我们的动机是原子力显微镜(AFM)图像处理的应用,需要解决分子生物学中的一个核心问题,旨在获得单个细胞的完整转录谱,一个快照,显示哪些基因正在表达,表达到什么程度。Reed等人(单分子转录谱分析与AFM,纳米技术,18:4,2007)表明,转录谱分析问题减少到对生物分子主干长度进行高精度测量,精确到20-25 bp (6-7.5 nm)。在这里,我们提出了一个使用AFM的图像处理和长度估计管道,接近于实现这些测量公差。特别是,我们在简单线性回归模型的训练系数上开发了一个有偏长度估计器,通过Beaton-Tukey函数进行双加权,其特征域受James-Stein收缩约束以避免过拟合。在可扩展性和解决模型选择问题方面,该公式包含了我们研究的模型。
Image analysis and length estimation of biomolecules using AFM.
There are many examples of problems in pattern analysis for which it is often possible to obtain systematic characterizations, if in addition a small number of useful features or parameters of the image are known a priori or can be estimated reasonably well. Often the relevant features of a particular pattern analysis problem are easy to enumerate, as when statistical structures of the patterns are well understood from the knowledge of the domain. We study a problem from molecular image analysis, where such a domain-dependent understanding may be lacking to some degree and the features must be inferred via machine-learning techniques. In this paper, we propose a rigorous, fully-automated technique for this problem. We are motivated by an application of atomic force microscopy (AFM) image processing needed to solve a central problem in molecular biology, aimed at obtaining the complete transcription profile of a single cell, a snapshot that shows which genes are being expressed and to what degree. Reed et al (Single molecule transcription profiling with AFM, Nanotechnology, 18:4, 2007) showed the transcription profiling problem reduces to making high-precision measurements of biomolecule backbone lengths, correct to within 20-25 bp (6-7.5 nm). Here we present an image processing and length estimation pipeline using AFM that comes close to achieving these measurement tolerances. In particular, we develop a biased length estimator on trained coefficients of a simple linear regression model, biweighted by a Beaton-Tukey function, whose feature universe is constrained by James-Stein shrinkage to avoid overfitting. In terms of extensibility and addressing the model selection problem, this formulation subsumes the models we studied.