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放射自显影片上的定标带:DNA指纹图谱评分的精密度研究。

Sizing bands on autoradiograms: a study of precision for scoring DNA fingerprints.

作者信息

Galbraith D A, Boag P T, Gibbs H L, White B N

机构信息

Department of Biology, Queen's University, Kingston, Ontario, Canada.

出版信息

Electrophoresis. 1991 Feb-Mar;12(2-3):210-20. doi: 10.1002/elps.1150120218.

Abstract

We replicated DNA fingerprints of snapping turtles (Chelydra serpentina) and hypervariable restriction fragments of red-winged blackbirds (Agelaius phoeniceus) to estimate the between-blot and between-lane components of variance in molecular weights of restriction fragments. Molecular weight standards were included in every lane, and bands were sized using a sonic digitizer. In both studies, a strong positive correlation was found between band size and coefficient of variation (CV; mean = 0.7%). In the DNA fingerprint study, 26% of the variance in estimates of band size was due to differences between blots, 10% due to differences between lanes on the same blot, and 64% due to error in the digitizing process. In the restriction fragment length polymorphism (RFLP) study, 16% of the variance was due to difference between lanes, and 84% to digitizing. Statistical models were developed to measure the effect of sizing error on identifying identical fragments in different lanes or on different blots, in categorizing distinct alleles, and in determining the size of bins in operational allele definitions. We suggest that the distance between bands be at least 2.8 standard deviations (SD) before they are declared different at alpha = 0.05, and 3.7 SD for alpha = 0.01. A variation in CVs strongly indicates that empirical relationships between SD and band size must be used to decide if two bands represent the same allele. Alleles must be at least 3.9 SD apart before the chance of assigning new observations in error falls below 0.05. We suggest that a minimum bin width of 16 SD is necessary before the chances of assigning a band to the wrong bin falls below 0.05.

摘要

我们复制了鳄龟(蛇鳄龟)的DNA指纹图谱以及红翅黑鹂(美洲红翼鸫)的高变限制性片段,以估计限制性片段分子量方差的印迹间和泳道间组分。每个泳道都包含分子量标准品,并且使用声波数字化仪对条带进行大小测定。在这两项研究中,均发现条带大小与变异系数(CV;平均值 = 0.7%)之间存在强正相关。在DNA指纹图谱研究中,条带大小估计值中26%的方差归因于印迹间差异,10%归因于同一印迹上泳道间差异,64%归因于数字化过程中的误差。在限制性片段长度多态性(RFLP)研究中,16%的方差归因于泳道间差异,84%归因于数字化。我们开发了统计模型,以衡量大小测定误差对识别不同泳道或不同印迹上的相同片段、对不同等位基因进行分类以及在操作等位基因定义中确定 bins 大小的影响。我们建议,在α = 0.05时,条带之间的距离至少为2.8个标准差(SD)时才判定它们不同,而在α = 0.01时则为3.7 SD。CV的变化强烈表明,必须使用SD与条带大小之间的经验关系来判定两条带是否代表相同的等位基因。在错误分配新观察值的概率降至0.05以下之前,等位基因之间的距离必须至少为3.9 SD。我们建议,在将条带错误分配到错误 bins 的概率降至0.05以下之前,bin宽度至少需要16 SD。

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