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Random error, definition

This is essentially the multi-dimensional definition of slope. It describes how changes in u depend on changes in x, y, and z. Note that we use du to examine systematic errors but (du) to examine random errors. [Pg.171]

The remaining errors in the data are usually described as random, their properties ultimately attributable to the nature of our physical world. Random errors do not lend themselves easily to quantitative correction. However, certain aspects of random error exhibit a consistency of behavior in repeated trials under the same experimental conditions, which allows more probable values of the data elements to be obtained by averaging processes. The behavior of random phenomena is common to all experimental data and has given rise to the well-known branch of mathematical analysis known as statistics. Statistical quantities, unfortunately, cannot be assigned definite values. They can only be discussed in terms of probabilities. Because (random) uncertainties exist in all experimentally measured quantities, a restoration with all the possible constraints applied cannot yield an exact solution. The best that may be obtained in practice is the solution that is most probable. Actually, whether an error is classified as systematic or random depends on the extent of our knowledge of the data and the influences on them. All unaccounted errors are generally classified as part of the random component. Further knowledge determines many errors to be systematic that were previously classified as random. [Pg.263]

Random errors are associated with the precision of the analytical method. According to the ICH definition, precision can be divided into ... [Pg.123]

A reference method is one which after exhaustive investigation has been shown to have negligible inaccuracy in comparison with its imprecision [International Federation of Clinical Chemistry (IFCC), 1979]. With its comparison of inaccuracy and imprecision this definition clearly refers to the principles of quality control in clinical chemistry. Indeed, statistical models such as Youden plots are used to find out whether the error in a pair of results happens by chance (imprecision of the method) or is systematic (inaccuracy) (Youden, 1967). If the results are close to the true values, inaccuracy is negligible in comparison with imprecision. As demonstrated earlier, each analytical procedure has a certain degree of imprecision consequently, the total absence of systematic error can never be proved. Only as the influence of a systematic error is evident in comparison with the influence of chance or random error can the systematic error be demonstrated. [Pg.144]

Final Caution. The Student t distribution is to be used when the numerical value to which it attaches is a mean of a definite number of direct observations or is a numerical result calculated from such a mean by a procedure that introduces no uncertainties comparable in magnitude to the random errors of the direct observations. This is notihe case for the specific rotation [a]j discussed above. The uncertainty contribution to the final result that is due to random errors in the raw data on optical rotations Oy is not large compared to the contributions due to the estimated uncertainties in the other variables (particularly Vand Z) that are required for calculating the final result The number of degrees of... [Pg.61]

Some of the concepts used in defining confidence limits are extended to the estimation of uncertainty. The uncertainty of an analytical result is a range within which the true value of the analyte concentration is expected to lie, with a given degree of confidence, often 95%. This definition shows that an uncertainty estimate should include the contributions from all the identifiable sources in the measurement process, i.e. including systematic errors as well as the random errors that are described by confidence limits. In principle, uncertainty estimates can be obtained by a painstaking evaluation of each of the steps in an analysis and a summation, in accord with the principle of the additivity of variances (see above) of all the estimated error contributions any systematic errors identified... [Pg.79]

One study has suggested that researchers looking for a connection between aluminium and Alzheimer s disease may have ignored the most important source of aluminium for the average person—foodstuffs that contain aluminium additives (36). The results implied that aluminium, added to such foods as anticaking agents, emulsifiers, thickeners, leaveners, and stabilizers, may have long-term adverse effects on health. However, the small sample size hampers any definitive conclusions, the odds ratios were very unstable, and the study had limited statistical power to rule out random errors. [Pg.99]

Fulk (1995) usefully identifies two types of variability (random and systematic error) and three ways in which this may become manifest (within-test, within-laboratory and between laboratories). In a conventional concentration-response experiment, the random occurrence of variability within an experiment will give rise to error around the fitted regression line, i.e. it will make the estimate of toxicity less precise. By contrast, non-random occurrence of these factors between experiments or laboratories can result in different estimates of toxicity, leading to bias. However, testing on different occasions or in different laboratories is also subject to random errors. As a result, the variability that we see is usually a combination of random and systematic errors. Variability resulting from random errors is, by definition, difficult to address but systematic errors can be... [Pg.46]

Tmeness is a measure of the systematic error (<5M) of the calculated result introduced by the analytical method from its theoretical true/reference value. This is usually expressed as percent recovery or relative bias/error. The term accuracy is used to refer to bias or trueness in the pharmaceutical regulations as covered by ICH (and related national regulatory documents implementing ICH Q2A and Q2B). Outside the pharmaceutical industry, such as in those covered by the ISO [20,21] or NCCLS (food industry, chemical industry, etc.), the term accuracy is used to refer to total error, which is the aggregate of both the systematic error (trueness) and random error (precision). In addition, within the ICH Q2R (formerly, Q2A and Q2B) documents, two contradictory definitions of accuracy are given one refers to the difference between the calculated value (of an individual sample) and its true value... [Pg.117]

Total Error or Measurement Error The measurement error of an analytical procedure expresses the closeness of agreement between the value measured and the value that is accepted either as a conventional true value or an accepted reference value. This is also the definition of accuracy in ICH Q2R. This closeness of agreement represents the sum of the systematic and random errors, that is, the total error associated with the observed result. Consequently, the measurement error is the expression of the sum of the trueness and precision, that is, the total error [19,22]. [Pg.118]

This definition of makes the relative contributions of the terms t in Eq. (30a) independent of At, and therefore equalizes the data sets with different numbers of observation. Relationship (73) assumes that for data set with redundant observations increases as. Such an increase can be caused by the fact that the number of sources of random errors may increase proportionally to the number of simultaneous measurements. For example, increasing spectral and/or angular resolution in remote-sensing measurements likely results in a decrease of the quality of a single measurement due to increased complexity of the instrumentation and calibration. However, the assumption given by Eq. (73) is of intuitive character since it is not based on... [Pg.99]

For determination of the range of parameter values consistent with the data, one typically chooses P s 0.32, where P is the probability that the value of is due to random errors in the data. When the value of P exceeds 0.32, there is less than a 32% chance that the parameter value is consistent with the data. When the value of P is less than 0.32, there is a 68% chance that the parameter value is consistent with the data, which is the usual definition of a standard deviafioit. [Pg.123]

It is most important to note that the procedures used for combining random and systematic errors are completely different. This is because random errors to some extent cancel each other out, whereas every systematic error occurs in a definite and known sense. Suppose, for example, that the final result of an experiment, x, is given by x = a + b. If a and b each have a systematic error of -i-l, it is clear that the systematic error in x is +2. If, however, a and b each have a random error of 1, the random error in x is not 2 this is because there will be occasions when the random error in a is positive while that in b is negative (or vice versa). [Pg.32]

Systematic errors have a definite value and an assignable cause and are of the same magnitude for replicate measurements made in the same way. Systematic errors lead to bias in measurement results. Bias is illustrated by the two curves in Figure al-2, which show the frequency distribution of replicate results in the analysis of identical samples by two methods that have random errors of identical size. Method A has no bia.s so that the mean is the true value. Method B has a bias that is given by... [Pg.494]

Figure 6.28 Definition of systematic and random errors in a measurement series (DIN 1319-1, 1995). The dashed curve displays the scatter of a number of... Figure 6.28 Definition of systematic and random errors in a measurement series (DIN 1319-1, 1995). The dashed curve displays the scatter of a number of...
Every measurement process renders values that are not centered at the true value but show some offset from it. These differences are often called errors. There are two types of error, systematic and random. A systematic error is a constant offset, whereas a random error is different between subsequent measurements, and this difference cannot be predicted. One approach of expressing the information gained from an experiment is to provide a best estimate of the measurand and information about systematic and random error values (in the form of an error analysis see, for example, Bevington and Robinson, 2003 Taylor, 1997). Another approach, the GUM approach, is to express the result of a measurement as a best estimate of the measurand together with an associated measurement uncertainty, which combines systematic and random errors on a common probabilistic basis. Figure 6.28 explains graphically the definitions for random and systematic errors and the corrections applied to the latter. Figure 6.29 shows the treatment of systematic and random errors in the course of an uncertainty analysis. [Pg.129]

Definition Measured quantity value minus a reference quantity value [25]. Description Error is the sum of systematic and random error. [Pg.141]

This will effectively create a tube surrounding all the calibration points. This approach requires optimisation of eqn (6.11), although constraints (6.10a) and (6.10b) are obviously not useful here. However this may be solved quite easily if we consider a value instead of unity. Such a value is denoted e and is called the width of the band or error tolerance or, simply, the 8-band. The conceptual idea implicit in e is very familiar to analytical chemists because if - by definition - the calibration points minimise their (overall) distance to the hyperplane, e represents no more than the residuals of the calibration fit. Thus, if we were to include all samples in the e-band, e would equal the largest difference between the target concentration of the samples and the values predicted by the SVR model. However, we know that some calibration points may be wrong and that random errors occur during calibration and the measurement of the unknowns and, therefore, it would be wise to allow the algorithm some flexibility, in the same way as was discussed for SVC. [Pg.396]

It must be stressed that the CMC value obtained from (4.6) is a function of the contribution factors Oi, 02, and /3j. In other words, the CMC depends on the solution properties employed in the determination and therefore differs with the method used. For this reason, measured CMC values define a narrow concentration range. The CMC values obtained from the solution properties mainly due to a monomeric surfactant contribution are found to be less than those due to a surfactant micelle contribution, as can be seen in Fig. 4.6. In this case, random errors are taken into account for the CMC determination methods. For example, the CMC value obtained from surface tension measurements is less than that obtained from turbidity. In the literature, however, CMCs have often been presented as definite concentra-tions, especially since the appearance of a separation model for micelliz-... [Pg.50]

Uncertainty expresses the range of possible values that a measurement or result might reasonably be expected to have. Note that this definition of uncertainty is not the same as that for precision. The precision of an analysis, whether reported as a range or a standard deviation, is calculated from experimental data and provides an estimation of indeterminate error affecting measurements. Uncertainty accounts for all errors, both determinate and indeterminate, that might affect our result. Although we always try to correct determinate errors, the correction itself is subject to random effects or indeterminate errors. [Pg.64]

X-ray emission spectrography, in common with other analytical methods, is subject to errors of different kinds. Lacking better information, we shall usually assume these errors to be independent and random. (Drift caused by changes in the electronic system is definitely not random.) Before we consider errors in general, we shall examine one that is not only important and unavoidable, but that also sets x-ray... [Pg.269]

The advantage of the measures as suggested here is that they point into the same direction as it is done by the verbal definitions. High precision and a high degree of accuracy, respectively, are characterized by high numerical values of the measures which approximate to 1 in the ideal case (absence of random and systematic deviations, respectively) and approximate to 0 if the deviations approach to 100%. In the worst cases, the numerical values prec(x) and acc(x) become negative which indicates that the relative random or systematic error exceeds 100%. [Pg.210]

The guidelines provide variant descriptions of the meaning of the term linearity . One definition is, ... ability (within a given range) to obtain test results which are directly proportional to the concentration (amount) of analyte in the sample [12], This is an extremely strict definition, one which in practice would be unattainable when noise and error are taken into account. Figure 63-la schematically illustrates the problem. While there is a line that meets the criterion that test results are directly proportional to the concentration of analyte in the sample , none of the data points fall on that line, therefore in the strictest sense of the phrase, none of the data representing the test results can be said to be proportional to the analyte concentration. In the face of nonlinearity of response, there are systematic departures from the line as well as random departures, but in neither case is any data point strictly proportional to the concentration. [Pg.424]

No definitive conclusions can be drawn concerning a possible role of rifaximin in preventing major complications of diverticular disease. Double-blind placebo-controlled trials with an adequate sample size are needed. However, such trials are difficult to perform considering the requirement of a large number of patients. Assuming a baseline risk of complications of diverticular disease of 5% per year [2], a randomized controlled trial able to detect a 50% risk reduction in complications should include 1,600 patients per treatment group considering a power of 80% (1 - (3) and an a error of 5%. [Pg.113]

Accuracy is often used to describe the overall doubt about a measurement result. It is made up of contributions from both bias and precision. There are a number of definitions in the Standards dealing with quality of measurements [3-5]. They are only different in the detail. The definition of accuracy in ISO 5725-1 1994, is The closeness of agreement between a test result and the accepted reference value . This means it is only appropriate to use this term when discussing a single result. The term accuracy , when applied to a set of observed values, describes the consequence of a combination of random variations and a common systematic error or bias component. It is preferable to express the quality of a result as its uncertainty, which is an estimate of the range of values within which, with a specified degree of confidence, the true value is estimated to lie. For example, the concentration of cadmium in river water is quoted as 83.2 2.2 nmol l-1 this indicates the interval bracketing the best estimate of the true value. Measurement uncertainty is discussed in detail in Chapter 6. [Pg.58]

An error is the difference between an individual result and the true value of the quantity being measured. Since true values cannot be known exactly, it follows, from the above definition, that errors cannot be known exactly either. Errors are usually classified as either random or systematic. [Pg.157]


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See also in sourсe #XX -- [ Pg.66 ]




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