Fast automated cell phenotype image classification

被引:129
作者
Hamilton, Nicholas A. [1 ]
Pantelic, Radosav S.
Hanson, Kelly
Teasdale, Rohan D.
机构
[1] Univ Queensland, ARC Ctr Bioinformat, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[3] Univ Queensland, Adv Computat Modelling Ctr, Brisbane, Qld 4072, Australia
关键词
D O I
10.1186/1471-2105-8-110
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: 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. Results: 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. Conclusion: 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.
引用
收藏
页数:8
相关论文
共 27 条
  • [1] [Anonymous], LIBSVM-A Library for Support Vector Machines
  • [2] [Anonymous], IMAGEJ
  • [3] LIFEdb: a database for functional genomics experiments integrating information from external sources, and serving as a sample tracking system
    Bannasch, D
    Mehrle, A
    Glatting, KH
    Pepperkok, R
    Poustka, A
    Wiemann, S
    [J]. NUCLEIC ACIDS RESEARCH, 2004, 32 : D505 - D508
  • [4] Bishop CM., 1995, Neural networks for pattern recognition
  • [5] Flow cytometry smaller and better
    Bonetta, L
    [J]. NATURE METHODS, 2005, 2 (10) : 785 - +
  • [6] A graphical model approach to automated classification of protein subcellular location patterns in multi-cell images
    Chen, Shann-Ching
    Murphy, Robert F.
    [J]. BMC BIOINFORMATICS, 2006, 7 (1)
  • [7] Objective clustering of proteins based on subcellular location patterns
    Chen, X
    Murphy, RF
    [J]. JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2005, (02): : 87 - 95
  • [8] Automatic identification of subcellular phenotypes on human cell arrays
    Conrad, C
    Erfle, H
    Warnat, P
    Daigle, N
    Lörch, T
    Ellenberg, J
    Pepperkok, R
    Eils, R
    [J]. GENOME RESEARCH, 2004, 14 (06) : 1130 - 1136
  • [9] CORTES C, 1995, MACH LEARN, V20, P273, DOI 10.1023/A:1022627411411
  • [10] Fink J.L., 2006, NUCL ACIDS RES, V34