Rogers Salman S, Waigh Thomas A, Zhao Xiubo, Lu Jian R
School of Physics and Astronomy, University of Manchester, Manchester M60 1QD, UK.
Phys Biol. 2007 Oct 9;4(3):220-7. doi: 10.1088/1478-3975/4/3/008.
We present a new particle tracking software algorithm designed to accurately track the motion of low-contrast particles against a background with large variations in light levels. The method is based on a polynomial fit of the intensity around each feature point, weighted by a Gaussian function of the distance from the centre, and is especially suitable for tracking endogeneous particles in the cell, imaged with bright field, phase contrast or fluorescence optical microscopy. Furthermore, the method can simultaneously track particles of all different sizes, and allows significant freedom in their shape. The algorithm is evaluated using the quantitative measures of accuracy and precision of previous authors, using simulated images at variable signal-to-noise ratios. To these we add new tests: the error due to a non-uniform background, and the error due to two particles approaching each other. Finally the tracking of particles in real cell images is demonstrated. The method is made freely available for non-commercial use as a software package with a graphical user-interface, which can be run within the Matlab programming environment.
我们提出了一种新的粒子跟踪软件算法,该算法旨在在光照水平变化很大的背景下准确跟踪低对比度粒子的运动。该方法基于围绕每个特征点的强度的多项式拟合,并由距中心距离的高斯函数加权,特别适用于跟踪通过明场、相差或荧光光学显微镜成像的细胞内源性粒子。此外,该方法可以同时跟踪所有不同大小的粒子,并在其形状上给予很大的自由度。使用先前作者的准确性和精确性定量测量方法,通过可变信噪比的模拟图像对该算法进行评估。在此基础上,我们增加了新的测试:由于背景不均匀导致的误差,以及由于两个粒子相互靠近导致的误差。最后展示了在真实细胞图像中对粒子的跟踪。该方法作为一个带有图形用户界面的软件包免费提供给非商业用户,可在Matlab编程环境中运行。