Mark H F, Parmenter M, Campbell W, Mark R, Zolnierz K, Dunwoodie D, Hann E, Airall E, Santoro K, Mark Y
Department of Pathology, Rhode Island Hospital, Providence 02903.
Cytogenet Cell Genet. 1993;62(1):13-8. doi: 10.1159/000133435.
The present study stemmed from a need for a rapid means of deriving reproducible chromosome measurements. An internal set of standards can serve as the basis for routine, easy, and reliable morphometric comparisons. In this study, a total of 100 karyotyped metaphases were analyzed using the Nestler Run-Mate, a computerized curvilinear measuring tool. The null hypothesis tested was that there are no significant differences between chromosomal relative-length values obtained via this previously untested approach and those cited in ISCN (1985). The results indicate that this new method is not only feasible and adequate but has advantage over the conventional approach, which requires the use of a projector and screen to measure chromosomes in unkaryotyped metaphase spreads; further, it is less expensive and easier than using computerized digitizing tablets, a conclusion supported by time-and-effort measurements. Immediately obvious applications include routine use in clinical cytogenetics laboratories, as well as for fractional length estimations in fluorescent in situ hybridization studies performed in research laboratories that do not have access to expensive automated instrumentation.
本研究源于对一种获取可重复染色体测量值的快速方法的需求。一套内部标准可作为常规、简便且可靠的形态测量比较的基础。在本研究中,使用Nestler Run-Mate(一种计算机化曲线测量工具)对总共100个核型中期相进行了分析。所检验的零假设是,通过这种此前未经测试的方法获得的染色体相对长度值与《人类细胞遗传学国际命名体制(1985)》中引用的值之间不存在显著差异。结果表明,这种新方法不仅可行且足够,而且相对于传统方法具有优势,传统方法需要使用投影仪和屏幕来测量未进行核型分析的中期相 spreads 中的染色体;此外,它比使用计算机化数字化平板电脑成本更低且更简便,这一结论得到了时间和精力测量的支持。立即可见的应用包括在临床细胞遗传学实验室的常规使用,以及在没有昂贵自动化仪器的研究实验室进行的荧光原位杂交研究中的片段长度估计。