Mascio L N, Verbeek P W, Sudar D, Kuo W L, Gray J W
Engineering Research Division/Biology and Biotechnology Research Program, Lawrence Livermore National Laboratory, Livermore, California, USA.
Cytometry. 1995 Jan 1;19(1):51-9. doi: 10.1002/cyto.990190107.
Algorithms have been developed to help automate the mapping of DNA sequences along metaphase chromosomes using fluorescence in situ hybridization (FISH). Custom algorithms computationally define chromosome boundaries and compute chromosomal medial axes. A dynamic regional thresholding (DRT) algorithm is described that allows reliable detection of hybridization domains, even when they differ substantially in size and intensity. Chromosomal locations are calculated by determining the fractional location of each hybridization probe along the medial axis of a metaphase chromosome relative to the short arm (FLpter). These algorithms were tested on simulated data and by analysis of the location of probes that had been previously mapped by other techniques. These algorithms allow probes to be mapped rapidly along human chromosomes with a precision of 2-3 Mb.
已经开发出算法,以帮助利用荧光原位杂交(FISH)实现沿中期染色体的DNA序列映射自动化。定制算法通过计算定义染色体边界并计算染色体中轴线。本文描述了一种动态区域阈值化(DRT)算法,该算法能够可靠地检测杂交域,即使它们在大小和强度上有很大差异。通过确定每个杂交探针沿中期染色体中轴线相对于短臂(FLpter)的分数位置来计算染色体位置。这些算法在模拟数据上进行了测试,并通过分析先前用其他技术定位的探针位置进行了验证。这些算法能够使探针沿着人类染色体快速定位,精度达到2-3 Mb。