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False positives and negatives

Long and Winefordner along with several other authors agree on a value of k = 3, which allows a confidence level of 99.86% if the values of xb follow a normal distribution, and 89% if the values of Xb do not follow a normal distribution. A value of k = 2 has also been used by some workers, but this decreases the confidence level in Cl. The definition of LOD was later expanded on by lUPAC in 1995 to include the probabilities of false positives and negatives. [Pg.64]

According to this system, when 3-4 points are accumulated (depending on the application), then a confirmation is said to be made. However, human judgment should still play a role because the point assignments are arbitrary and actual rates of false positives and negatives are typically unknown. It makes sense that the more points that are gathered in an analysis should lead to a confirmation, but MS should not be considered as the only tool in the analysis, and all the pieces of information should make sense and point in the same direction for most accurate confirmations. [Pg.765]

Alternatively, samples are quickly screened by thermal methods, such as DSC or ITC. This alternative approach eliminates the necessity for stability set-downs hence cycle times and sample consumption are reduced. However, the data obtained are difficult to interpret and may be misleading false positives and negatives are routinely encountered [14]. [Pg.24]

Mass spectrometry (MS) is highly selective. The ability to further perform tandem mass spectrometry (MS/MS) analysis when a compound is detected to confirm the detection virtually eliminates false positive and negative alarms. But MS/MS analysis must be completely automated for the average GI to be able to perform it. A clever hand-held chemical and biological mass spectrometer has been developed that weighs only 4.3 pounds. The problem with the unit is production of the necessary vacuum, which requires 35 amps at 24 volts. Thus, battery-operated portable mass spectrometry is not yet available. [Pg.81]

False-Positive and -Negative Errors with Sample Size = 50... [Pg.7]

Figures 1 and 2 illustrate how the determination of false-positive and -negative inference errors varies with sample size. In Figure 1, the sample size is 50. To be 95 percent confident that an observed incidence difference between the experimental and control groups is really evidence of carcinogenicity rather than sampling variation, the difference in cancer rates between the two groups must be at least 23 percent. Figures 1 and 2 illustrate how the determination of false-positive and -negative inference errors varies with sample size. In Figure 1, the sample size is 50. To be 95 percent confident that an observed incidence difference between the experimental and control groups is really evidence of carcinogenicity rather than sampling variation, the difference in cancer rates between the two groups must be at least 23 percent.
At most concentrations, inductively coupled plasma mass spectrometry exhibited higher precision and accuracy than the other techniques, but also the highest rates of false positives and negative results. [Pg.4]

The decision on what type of screen to use in FBDD is affected by many different factors availability of protein for screening, compound selection, throughput, turnaround and rate of false positives and negatives. The resolution of these questions from target assessment directly impact the possibilities in this section. If there is not sufficient protein for a biophysical screen, a biochemical screen is the only choice. Protein that is not stable for... [Pg.19]

Figure 8 Boxplots of normalized intensity values across arrays, boxplots facilitate comparison of sample distributions and dynamic range across microarrays. If the microarrays follow different data distributions increased false positive and negative rates may be demonstrated. The depicted signal is the log2 of the normalized feature signal intensity. Figure 8 Boxplots of normalized intensity values across arrays, boxplots facilitate comparison of sample distributions and dynamic range across microarrays. If the microarrays follow different data distributions increased false positive and negative rates may be demonstrated. The depicted signal is the log2 of the normalized feature signal intensity.
The DEMETRA models have been optimized to minimize the number of false negatives in order to achieve a safer regulatory application. Conversely, evaluation using only squared statistical parameters (such as R2), which deal with false positives and negatives in the same manner, is typical in QSAR modeling. [Pg.195]

The predictive performance of a CM is often expressed in terms of a contingency table (Table 18.1) containing the numbers of true and false positive and negative predictions made by the CM, and in terms of the CM s Cooper statistics, which are derived from the contingency table. Definitions of the Cooper statistics are provided in Table 18.2. [Pg.395]

Protease assays based on the FLT of PT14 are especially attractive due to the long lifetime of the dye of 14 ns that allows the discrimination of the lifetimes of short-lived fluorescent compounds from that of PT14. Thus, the rate of false-positive and -negative results can be reduced. The major... [Pg.40]

False positive and negative results, i.e. for samples containing <15 ppb a positive result using the kit would be "false, for samples containing >15 ppb a negative result would be false."... [Pg.44]

RADIOIMMUNOASSAY (RIA) One method used for anabolic steroid detection. This method is inadequate as it produces false positive and negative readings. [Pg.6]


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