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Class probability

The recent explosion in the discovery of new myosin genes has led to the idea that myosins from different classes probably co-exist in cells. This has raised the obvious question as to what functions these myosins subserve within cells. Up to now, only the genes have been cloned for many of the 35 unique myosins. But this is not a question that can be answered solely by cloning rather, it is absolutely imperative to biochemically characterize these proteins if we are to understand their physiological properties. One way to do this is to express the entire protein or parts of the proteins in bacteria, yeast, or insect cells, and to then purify and characterize... [Pg.74]

No a priori assumptions about the distribution of data or class probability are required. [Pg.264]

Fig. 8.4. A priori probability density functions (pdfs) of two classes and their resulting assignments after weighting them with their corresponding class probabilities. For a given feature value along the x-axis, the higher of the corresponding y-axis values decides the class for that value. Two types of errors are possible with this scheme, namely the misclassification of class 1 as class 2 (horizontal stripes) and the misclassification of class 2 as class 1 (vertical stripes/shaded). The colored regions indicate the relative probabilities of such errors. Errors can be explicitly understood and the contribution of each feature to classification can be quantitatively measured... Fig. 8.4. A priori probability density functions (pdfs) of two classes and their resulting assignments after weighting them with their corresponding class probabilities. For a given feature value along the x-axis, the higher of the corresponding y-axis values decides the class for that value. Two types of errors are possible with this scheme, namely the misclassification of class 1 as class 2 (horizontal stripes) and the misclassification of class 2 as class 1 (vertical stripes/shaded). The colored regions indicate the relative probabilities of such errors. Errors can be explicitly understood and the contribution of each feature to classification can be quantitatively measured...
Configurational data on diampromide and its relatives indicate, therefore, that the assumed analogy with the methadone class is not justified and that the two classes probably differ in their binding modes at the receptor.(91) Degrees of receptor stereoselectivity are generally less in the anilides (Table... [Pg.320]

It turns out that there are two groups of elements, namely such which require El(L) changes from substrate to product of just more than -0.22 V to overcome enhanced possible binding by formation of additional binding sites (Al, Cu) and another for which this difference must be larger than -0.3 V (Mg, V, Fe(in), Zn, Cd). The actual hydrolases belong to the latter class, probably due to the very low El(L) values of their most common carboxylate or phosphate products. [Pg.139]

Equivalence class Probability ng og2rig -log2 P -Pg log2 p ... [Pg.241]

The SCS, applied to the MR spectra, distinguished between normal tissue and HCC with 100% sensitivity and specificity (i.e. 100% accurate). All spectra were crisply classified that is, class probability was always larger than 75%. Using a separate classifier, cirrhotic liver tissue and HCC were distinguished with a sensitivity and specificity of 95.8% and 88.9%, respectively. The overall crispness was 84%. An overall accuracy of 98.4% was obtained when specimens classified as fuzzy were excluded. A third classifier was developed to distinguish normal from cirrhotic liver. These were distinguished with a sensitivity and specificity of 96.8% and 85.4%, respectively. The overall crispness of the data was, however, low at 79.7%. Here the SCS-based analysis misclassified one cirrhotic and four normal tissue samples, and 12 cirrhotic and four normal tissue samples were fuzzy (class probability less than 75%). When the fuzzy specimens were excluded, an overall accuracy of 92.1% was obtained. The spectral regions used in each of the classifiers and the classification accuracies are summarized in Table 2. [Pg.99]

The presence of lymph node metastases was predicted with a sensitivity of 97% and specificity of 94% (Table 2). The overall crispness of the data was 95.1 %, that is, 3 of the total 61 samples were classified as fuzzy (class probability less than 75%). An overall 95.0% accuracy for the test was obtained when specimens classified as fuzzy were excluded.83... [Pg.102]

Mean z-score -2.18 Structure conservation index 0.97 SVM decision value 2.39 SVM RNA-class probability 0.993311 Prediction RNA... [Pg.509]

RNAz assists in the final classification by providing an overall RNA-class probability, or p-value. It is important to know that this is not a p-value in a strict statistical sense, simply because there is no underlying statistical model. Instead, RNAz uses a rather ad hoc machine learning technique to calculate this value. If p > 0.5, the alignment is classified as RNA. The false-positive rate at this cutoff was found to be 4 %, i.e., we expect four positive hits in 100 random alignments. For many applications it is useful to set a more stringent cutoff of p = 0.9 with an associated false-positive rate of 1 %. Reasons why estimations of false-positives must always be taken with caution are given in Note 6. [Pg.511]

In this example, the signal from both strands are almost indistinguishable and also the /> values are almost the same (0.993 and 0.999). RNAz still suggests the correct (forward) strand and displays a strand class probability ... [Pg.512]

RNAz uses a SVM algorithm for classification. The raw output of the SVM is the so-called decision-value. This real-valued number is positive if the prediction is RNA and negative otherwise. From this value we calculate the more intuitive RNA class probability or p-value, which is 0.5 for a decision value of 0. In some cases, the raw decision value can be more convenient than the p-value (e.g., to plot the distribution of RNAz results). [Pg.523]

The rates of addition of nucleophiles to carbonyl groups and the rates of elimination from the tetrahedral intermediates constitute another class, probably similar to the activated aromatic nucleophilic substitution. The carbonyl group is an electrophile, and no obvious source of any barrier exists, outside of desolvation. Therefore, a resemblance to Ritchies systems is found. No obvious relation between our kinetic nucleophilic characters (Nx) and the additions occurs, but a possible parallel to the equilibrium methylating powers, KYX (in Tables I and II), of the conjugate methylating agent of the... [Pg.52]

Four structural classes of c-type cytochromes thus are known today eukaryotic c, c, C3, and flavin-c. Other classes probably will be called for as structural information becomes available on more c proteins. These four classes probably represent independent evolutionary convergence on the use of a C. . . CH mode of attaching a heme group rather than divergence from a common ancestral prototype. Within each class, one... [Pg.538]

S (x - Xr) ] is the class probability density function which is assumed to follow a normal distribution. [Pg.193]

The evidence currently available on the antagonism of antiplatelet effects is insufficient to recommend that ibuprofen is not used with low-dose aspirin. Nevertheless, some have concluded that when patients taking low-dose aspirin for cardioprotection require long-term NSAIDs for inflammatory conditions, the use of diclofenac or naproxen would seem preferable to ibuprofen.A coxib was also suggested as an alternative,but the subsequent suggestion of an increased risk of serious cardiovascular effects with the coxibs (as a class ) probably precludes this. Recently the Commission on Human Medicines (CHM) in the UK has advised that there may be a small increased risk of thrombotic events with the non-selective NSAIDs, particularly when used at high doses and for long-term treatment. ... [Pg.145]

This concept allows a mathematical description of a single class of patterns. Outliers with deviating features lie outside the box. SIMCA gives for each unknown pattern a probability for each class. Patterns with very low probabilities for all classes probably Indicate "a new kind". [Pg.90]

Efforts to improve quality and integration or move the organization toward recognition as world class probably contribute to potency. But often it is the integration or the quality level itself that is the objective — regardless of impact on competitive position. One can have these things without improvement in competitive position. [Pg.49]

Rule induction is an artificial intelligence method that has been applied to the analysis of a number of chemical data sets. As the name implies, rule induction aims to extract rules from a set of data (descriptor variables) so as to classify the samples (compounds, objects) into two or more categories. The input to a rule induction algorithm is a number of test cases, a test set, and the output is a tree-structured series of rules, also known as a class probability tree. A popular rule induction algorithm is... [Pg.218]

Input-domain based category Equivalence classes Probability of execution of an equivalence class Distance between test cases in an equivalence class or correctness probability... [Pg.2306]

A group of reactions of trityl derivatives discovered by Stieglitz ( 1916) are shown in reactions (90a) to (90c) °. Such reactions have not been reported for other classes probably owing to synthetic difficulties for only in trityl and a few similar types does steric hindrance... [Pg.736]

As this value is a constant, it is clear that in order to establish the most probable model class, the numerator term p A Mi)P Mi M) = iP Mi M.) in Eq. 9 has to be maximized with respect to i. Usually, the process of model class selection consists of determining the posterior probabilities of all model classes in the set AT and ranking them accordingly, where the best model class is the one that results in the highest value of the quantity f,F(A, AT). Since most often equal prior model class probabilities are adopted, it suffices to compute the evidence values c, for all... [Pg.1526]


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See also in sourсe #XX -- [ Pg.80 ]




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