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Display methods

It is not necessary to build stmctures to use the Registry File. Compounds can also be searched for by using names, combinations of name fragments. Registry Numbers, molecular formulas, and in other ways. The display methods are the same. [Pg.1636]

Exploratory Data Analysis and Display Methods Visualization of Data Structures... [Pg.268]

Liang P et al. Analysis of altered gene expression by differential display. Methods Enzymol 1995 254 304—321. [Pg.111]

Gonsky R et al. Identification of rapid turnover transcripts overexpressed in thyroid tumors and thyroid cancer cell lines use of a targeted differential RNA display method to select for mRNA subsets. Nucleic Acids Res 1997 25 3823-3831. [Pg.115]

A traditional approach to reuse might factor the design as follows. Because the display of different shapes varies with the kind of shapes, we design a shape hierarchy. The display method is abstracted on the superclass—because shapes display themselves differently— and each subclass provides its own implementation. [Pg.485]

There are common pieces to the display method, such as computing the font size appropriate for a particular shape given its inner bounding box and printing the location in the computed font. Hence we implement a computeFont and printLocation method on the superclass (marked protected in Java so that it is subclass-visible), class Shape ... [Pg.485]

Begin with the mind-set that the display methods would be different and then seek the common pieces that could be shared between them. [Pg.487]

Display methods (EP, NLM) can be considered as clustering techniques, when no apriori information is given about the subdivision of the dataset into categories. However, with the name of cluster analysis, we will denote the techniques working with the whole multivariate information in the following way. [Pg.130]

Sometimes, in the field of food chemistry, display methods have been used to detect clusters, while clustering techniques have been u to confirm the subdivision into categories, and then as classification methods. [Pg.131]

To analyze the differenees of protein expression profiles between caneer tissues and corresponding non-caneerous tissues, the proteomic differential display method was used. In this method, 2-DE and MS were used to identify the proteins. We first separated proteins from caneer tissues and eorresponding non-cancerous tissues by 2-DE. Then the protein spots of the samples from eaneer tissues were compared to the spots of the samples from corresponding non-eaneerous tissues by using software for proteomie differential display. [Pg.35]

Particular protein spots for which expression was different between eancerous and non-cancerous tissues were cut out from the gels, and were identified by means of MS. Figure 1 shows a workflow of these methods. The proteomic differential display method is a common method to analyze the profiling of protein expression. Usually 2-DE and MS have been used. [Pg.35]

P.M. O Brien, R. Ai tken, Antibody Phage Display Methods and Protocols, Humana Press, Totowa, NJ 2001. [Pg.64]

Temperature should be strictly controlled in the microwave oven with a temperature probe that has a feedback mechanism to regulate the energy output of the microwave oven and thus maintains the optimal temperature. Alternatively, temperature can be controlled by placing a water load in the chamber of the microwave oven, which absorbs extra energy and provides humidity, slowing the evaporation of reagents. In addition, hot spots in the chamber should be avoided by using the neon bulb display method (Chapter 5). [Pg.166]

The procedure for epitope mapping by the phage display method involves biopanning, amplification, assay for positive colonies, DNA isolation, and sequencing. Some steps of the procedure must be performed at the same time. Therefore, we describe the protocols in Subheadings 3.1. and 3.2. on a day-by-day manner. All steps of biopanning and phage amplification should be carried out under sterile conditions, when possible. [Pg.136]

Figure 7. Ribbon diagram of the EPO-receptor bound to a disulfide-bridged agonist peptide, isolated by phage display methods (Brookhaven file 1 EBP). Figure 7. Ribbon diagram of the EPO-receptor bound to a disulfide-bridged agonist peptide, isolated by phage display methods (Brookhaven file 1 EBP).
Unsupervised learning methods - cluster analysis - display methods - nonlinear mapping (NLM) - minimal spanning tree (MST) - principal components analysis (PCA) Finding structures/similarities (groups, classes) in the data... [Pg.7]

Certainly it is possible to apply also other display methods for the visualization of such complex environmental data, as particulate emissions. TREIGER et al. [1993 1994] describe the study of different aerosol samples by nonlinear mapping of electron probe microanalysis data. Different interpretable groups of chemical elements which determine the composition of aerosol samples can be obtained. More recent work by WIENKE and HOPKE [1994] and WIENKE et al. [1994] discuss the combination of different chemometric techniques for better graphical representation of aerosol particle data. The authors use receptor modeling with a minimal spanning tree combined with a neural network. [Pg.257]

Like any other kind of collection, the condition of tapa is highly dependent upon the quality of manufacture, the extent to which it has been used, the manner in which it has been used, the quality of storage, display methods, and the environment. [Pg.171]


See other pages where Display methods is mentioned: [Pg.247]    [Pg.422]    [Pg.364]    [Pg.254]    [Pg.69]    [Pg.70]    [Pg.60]    [Pg.487]    [Pg.69]    [Pg.262]    [Pg.268]    [Pg.376]    [Pg.310]    [Pg.73]    [Pg.74]    [Pg.74]    [Pg.132]    [Pg.36]    [Pg.113]    [Pg.44]    [Pg.247]    [Pg.1726]    [Pg.219]    [Pg.42]    [Pg.284]    [Pg.373]    [Pg.527]    [Pg.401]    [Pg.169]    [Pg.233]   
See also in sourсe #XX -- [ Pg.11 , Pg.97 ]




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