基于多光谱卷积稀疏编码的组织学切片分类。

Yin Zhou, Hang Chang, Kenneth Barner, Paul Spellman, Bahram Parvin
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引用次数: 101

摘要

基于图像的组织学切片分类在预测临床结果中起着重要作用。然而,由于存在较大的技术差异(例如,固定,染色)和生物异质性(例如,细胞类型,细胞状态),这项任务非常具有挑战性。在生物医学成像领域,为了可视化和/或量化的目的,不同的染色通常用于不同的感兴趣目标(例如,细胞/亚细胞事件),通过各种类型的显微镜生成多光谱数据(图像),因此,通过利用多光谱信息提供了学习生物成分特定特征的可能性。我们提出了一种基于卷积稀疏编码(CSC)的多光谱特征学习模型,该模型自动学习一组来自不同光谱的卷积滤波器组,以有效地发现组织的内在形态特征。然后通过空间金字塔匹配框架(SPM)对学习到的特征表示进行聚合,最后使用线性支持向量机进行分类。该系统已通过从癌症基因组图谱(TCGA)中收集的两个大规模肿瘤队列进行评估。实验结果表明,所提出的模型1)优于使用稀疏编码进行无监督特征学习的系统(例如PSD-SPM [5]);2)与基于生物先验知识(例如SMLSPM[4])的特征构建的系统竞争。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Classification of Histology Sections via Multispectral Convolutional Sparse Coding.

Classification of Histology Sections via Multispectral Convolutional Sparse Coding.

Classification of Histology Sections via Multispectral Convolutional Sparse Coding.

Classification of Histology Sections via Multispectral Convolutional Sparse Coding.

Image-based classification of histology sections plays an important role in predicting clinical outcomes. However this task is very challenging due to the presence of large technical variations (e.g., fixation, staining) and biological heterogeneities (e.g., cell type, cell state). In the field of biomedical imaging, for the purposes of visualization and/or quantification, different stains are typically used for different targets of interest (e.g., cellular/subcellular events), which generates multi-spectrum data (images) through various types of microscopes and, as a result, provides the possibility of learning biological-component-specific features by exploiting multispectral information. We propose a multispectral feature learning model that automatically learns a set of convolution filter banks from separate spectra to efficiently discover the intrinsic tissue morphometric signatures, based on convolutional sparse coding (CSC). The learned feature representations are then aggregated through the spatial pyramid matching framework (SPM) and finally classified using a linear SVM. The proposed system has been evaluated using two large-scale tumor cohorts, collected from The Cancer Genome Atlas (TCGA). Experimental results show that the proposed model 1) outperforms systems utilizing sparse coding for unsupervised feature learning (e.g., PSD-SPM [5]); 2) is competitive with systems built upon features with biological prior knowledge (e.g., SMLSPM [4]).

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