scholarly journals Rounding error, an unexpected fault in the output from a recording spectrophotometer: implications for model discrimination

1993 ◽  
Vol 292 (1) ◽  
pp. 37-40 ◽  
Author(s):  
M L Cárdenas ◽  
A Cornish-Bowden

Although commonly ignored in discussions of experimental error, rounding may sometimes be the major source of error, especially with modern precision instruments: some recording spectrophotometers are optically and photometrically capable of making absorbance measurements with errors less than 0.0003, but provide no numerical information more precise than +/- 0.001. The problem may be diagnosed by a characteristic arrangement of points in a residual plot, which resembles the result of cutting a stroboscopic picture of a bouncing ball into several strips and modifying it by sliding the strips relative to one another to bring the points closer to the axis. Harmful effects of rounding error can be critical in experiments designed for model discrimination.

1995 ◽  
Vol 50 (5) ◽  
pp. 351-363 ◽  
Author(s):  
Michael McCloskey ◽  
Paul Macaruso

1983 ◽  
Vol 28 (1) ◽  
pp. 79-79
Author(s):  
Claire B. Ernhart

1977 ◽  
Vol 37 (03) ◽  
pp. 535-540 ◽  
Author(s):  
D. S Pepper ◽  
D Banhegyi ◽  
Ann Howie

SummaryPrevious work from this department, concerned with testing the potential thrombogenicity of therapeutic factor IX concentrates, demonstrated that following recalcification of factor IX concentrates thrombin was generated within 3-30 minutes of incubation (Sas et al. 1975). The test developed (known as the TGt 50 test) is a two-stage assay and was thus found to be time consuming, tedious and tended to become inaccurate with long incubation periods and a large number of samples. A semiautomatic version of the test is reported in which the synthetic peptide Bz-ILE-GLU-GLY-ARG-pNA (S-2222) is added to recalcified, diluted factor IX concentrate in the micro-cuvette of a multiple sample recording spectrophotometer. Information can be obtained on (a) the amount of Xa (if any) present prior to recalcification (b) the initial amount of Xa formed and (c) the time taken to activate all factor X to Xa. Direct graphical interpretation shows a number of qualitative differences between commercial preparations, but by either of the criteria (b) or (c) above, it is possible to place the different products into “activated” and “non activated” groups such that both the Xa generation times and TGt 50 tests identify the same two groups of products. This agreement also indicates that the TGt 50 test is independent of the intrinsic factor V levels in the various concentrates.


1972 ◽  
Vol 28 (03) ◽  
pp. 447-456 ◽  
Author(s):  
E. A Murphy ◽  
M. E Francis ◽  
J. F Mustard

SummaryThe characteristics of experimental error in measurement of platelet radioactivity have been explored by blind replicate determinations on specimens taken on several days on each of three Walker hounds.Analysis suggests that it is not unreasonable to suppose that error for each sample is normally distributed ; and while there is evidence that the variance is heterogeneous, no systematic relationship has been discovered between the mean and the standard deviation of the determinations on individual samples. Thus, since it would be impracticable for investigators to do replicate determinations as a routine, no improvement over simple unweighted least squares estimation on untransformed data suggests itself.


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