Shah Shishir
University of Houston, Department of Computer Science, Houston, TX 77204-3010, USA.
J Microsc. 2007 Nov;228(Pt 2):211-26. doi: 10.1111/j.1365-2818.2007.01842.x.
The most commonly used molecular cytogenetic technique is fluorescence in situ hybridization (FISH). It has been widely applied in many areas of diagnosis and research, including pre-natal and post-natal screening of chromosomal aberrations, pre-implantation genetic diagnosis, cancer cytogenetics, gene mapping, molecular pathology and developmental molecular biology. The analysis of FISH images consists of detecting fluorescent dots, after which the number of dots per cell can be counted or their relative positions can be measured. A major impediment in the analysis of FISH specimens is signal (dot) quality, which is influenced by the hybridization efficiency and/or the sensitivity of the camera that records the images.
In this paper, we present an approach to improve the efficiency of detecting fluorescent signals in FISH images by recovering the radiance map of the camera. This allows us to generate a high-dynamic-range image wherein an extended range of the sample radiance captured by the camera can be visualized at distinct intensity values. The resulting higher-order numeric complexity of the transformed image is adjusted (or simplified) by examining the intensity distribution in each of the three colour channels (red, green and blue), and remapping the intensity values to generate a high-contrast image with a lower-order (compressed) dynamic range. The remapping is based on a criterion that optimizes the detection of the hybridized signals, allowing attenuation of saturated intensity values while amplifying low-intensity signals.
A simple dot-counting algorithm is used to automatically process 2000 FISH images. The images are taken for lymphocytes from cultured blood specimens for cytogenetic testing. Images are manually analyzed by an expert to obtain ground truth for dot counts. A quantitative analysis is performed by comparing results of automated dot detection on images before and after enhancement with the developed algorithms. In addition, common errors in dot counting due to split dots, dust, poor segmentation and overlapping signals are analyzed and the robustness of the developed approach against these errors evaluated. It is observed that dot-detection efficiency is increased by an average of 9% across all colour channels while reducing errors in missed and false dot counts.
Our proposed method and results demonstrate that dot-counting specificity and sensitivity can be improved by pre-processing and enhancing the image using the radiance curve of the camera and generating a high-contrast, remapped high-dynamic-range image prior to using any algorithm for dot counting.
最常用的分子细胞遗传学技术是荧光原位杂交(FISH)。它已广泛应用于诊断和研究的许多领域,包括产前和产后染色体畸变筛查、植入前基因诊断、癌症细胞遗传学、基因图谱绘制、分子病理学和发育分子生物学。FISH图像分析包括检测荧光点,之后可以计算每个细胞中的点数或测量它们的相对位置。FISH标本分析中的一个主要障碍是信号(点)质量,它受杂交效率和/或记录图像的相机灵敏度的影响。
在本文中,我们提出了一种通过恢复相机的辐射度图来提高FISH图像中荧光信号检测效率的方法。这使我们能够生成一个高动态范围图像,其中相机捕获的样本辐射度的扩展范围可以在不同的强度值下可视化。通过检查三个颜色通道(红色、绿色和蓝色)中每个通道的强度分布,并重新映射强度值以生成具有较低阶(压缩)动态范围的高对比度图像,来调整(或简化)变换后图像产生的更高阶数值复杂度。重新映射基于一个优化杂交信号检测的标准,允许衰减饱和强度值,同时放大低强度信号。
使用一个简单的点数算法自动处理2000张FISH图像。这些图像取自用于细胞遗传学检测的培养血液标本中的淋巴细胞。由专家对图像进行人工分析以获得点数的真实值。通过比较使用所开发算法增强前后图像上自动点检测的结果进行定量分析。此外,分析了由于点分裂、灰尘、分割不佳和信号重叠导致的点数常见错误,并评估了所开发方法对这些错误的鲁棒性。观察到在所有颜色通道上,点检测效率平均提高了9%,同时减少了漏计和误计的错误。
我们提出的方法和结果表明,在使用任何点数算法之前,通过利用相机的辐射度曲线对图像进行预处理和增强,并生成高对比度、重新映射的高动态范围图像,可以提高点数的特异性和灵敏度。