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A calibration curve plot showing limit of detection (LOD), limit of quantification (LOQ), dynamic range, and limit of linearity (LOL).. In analytical chemistry, a calibration curve, also known as a standard curve, is a general method for determining the concentration of a substance in an unknown sample by comparing the unknown to a set of standard samples of known concentration. [1]
Huber-White standard errors assume is diagonal but that the diagonal value varies, while other types of standard errors (e.g. Newey–West, Moulton SEs, Conley spatial SEs) make other restrictions on the form of this matrix to reduce the number of parameters that the practitioner needs to estimate.
Heteroskedasticity-consistent standard errors that differ from classical standard errors may indicate model misspecification. Substituting heteroskedasticity-consistent standard errors does not resolve this misspecification, which may lead to bias in the coefficients. In most situations, the problem should be found and fixed. [5]
The MSE either assesses the quality of a predictor (i.e., a function mapping arbitrary inputs to a sample of values of some random variable), or of an estimator (i.e., a mathematical function mapping a sample of data to an estimate of a parameter of the population from which the data is sampled).
The standard deviation is the square root of the variance. When individual determinations of an age are not of equal significance, it is better to use a weighted mean to obtain an "average" age, as follows: x ¯ ∗ = ∑ i = 1 N w i x i ∑ i = 1 N w i . {\displaystyle {\overline {x}}^{*}={\frac {\sum _{i=1}^{N}w_{i}x_{i}}{\sum _{i=1}^{N}w_{i}}}.}
It is a variant of MAPE in which the mean absolute percent errors is treated as a weighted arithmetic mean. Most commonly the absolute percent errors are weighted by the actuals (e.g. in case of sales forecasting, errors are weighted by sales volume). [3] Effectively, this overcomes the 'infinite error' issue. [4]