Hamilton Nicholas A, Pantelic Radosav S, Hanson Kelly, Teasdale Rohan D
ARC Centre in Bioinformatics, University of Queensland, Brisbane, Queensland 4072, Australia.
BMC Bioinformatics. 2007 Mar 30;8:110. doi: 10.1186/1471-2105-8-110.
The genomic revolution has led to rapid growth in sequencing of genes and proteins, and attention is now turning to the function of the encoded proteins. In this respect, microscope imaging of a protein's sub-cellular localisation is proving invaluable, and recent advances in automated fluorescent microscopy allow protein localisations to be imaged in high throughput. Hence there is a need for large scale automated computational techniques to efficiently quantify, distinguish and classify sub-cellular images. While image statistics have proved highly successful in distinguishing localisation, commonly used measures suffer from being relatively slow to compute, and often require cells to be individually selected from experimental images, thus limiting both throughput and the range of potential applications. Here we introduce threshold adjacency statistics, the essence which is to threshold the image and to count the number of above threshold pixels with a given number of above threshold pixels adjacent. These novel measures are shown to distinguish and classify images of distinct sub-cellular localization with high speed and accuracy without image cropping.
Threshold adjacency statistics are applied to classification of protein sub-cellular localization images. They are tested on two image sets (available for download), one for which fluorescently tagged proteins are endogenously expressed in 10 sub-cellular locations, and another for which proteins are transfected into 11 locations. For each image set, a support vector machine was trained and tested. Classification accuracies of 94.4% and 86.6% are obtained on the endogenous and transfected sets, respectively. Threshold adjacency statistics are found to provide comparable or higher accuracy than other commonly used statistics while being an order of magnitude faster to calculate. Further, threshold adjacency statistics in combination with Haralick measures give accuracies of 98.2% and 93.2% on the endogenous and transfected sets, respectively.
Threshold adjacency statistics have the potential to greatly extend the scale and range of applications of image statistics in computational image analysis. They remove the need for cropping of individual cells from images, and are an order of magnitude faster to calculate than other commonly used statistics while providing comparable or better classification accuracy, both essential requirements for application to large-scale approaches.
基因组革命推动了基因和蛋白质测序的快速发展,目前人们的注意力正转向所编码蛋白质的功能。在这方面,蛋白质亚细胞定位的显微镜成像已证明具有极高价值,并且自动荧光显微镜技术的最新进展使得能够高通量地对蛋白质定位进行成像。因此,需要大规模的自动化计算技术来有效地量化、区分和分类亚细胞图像。虽然图像统计在区分定位方面已证明非常成功,但常用的测量方法存在计算相对较慢的问题,并且通常需要从实验图像中逐个选择细胞,从而限制了通量和潜在应用范围。在此,我们引入阈值邻接统计,其本质是对图像进行阈值处理,并计算具有给定数量相邻高于阈值像素的高于阈值像素的数量。这些新颖的测量方法被证明能够在不裁剪图像的情况下,高速且准确地区分和分类不同亚细胞定位的图像。
阈值邻接统计应用于蛋白质亚细胞定位图像的分类。它们在两个图像集(可下载)上进行了测试,一个图像集中荧光标记的蛋白质在10个亚细胞位置内源性表达,另一个图像集中蛋白质被转染到11个位置。对于每个图像集,训练并测试了支持向量机。在内源性和转染图像集上分别获得了94.4%和86.6%的分类准确率。发现阈值邻接统计比其他常用统计方法提供了相当或更高的准确率,同时计算速度快一个数量级。此外,阈值邻接统计与哈拉里克测量方法相结合,在内源性和转染图像集上分别给出了98.2%和93.2%的准确率。
阈值邻接统计有潜力极大地扩展图像统计在计算图像分析中的应用规模和范围。它们无需从图像中裁剪单个细胞,并且比其他常用统计方法计算速度快一个数量级,同时提供相当或更好的分类准确率,这两者都是应用于大规模方法的基本要求。