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This plot is colored such that those points having a fold-change less than 2 (log 2 = 1) are shown in gray. In statistics, a volcano plot is a type of scatter-plot that is used to quickly identify changes in large data sets composed of replicate data. [1][2] It plots significance versus fold-change on the y and x axes, respectively.
Semi-log plot of the Internet host count over time shown on a logarithmic scale. A logarithmic scale (or log scale) is a method used to display numerical data that spans a broad range of values, especially when there are significant differences between the magnitudes of the numbers involved. Unlike a linear scale where each unit of distance ...
On a semi-log plot the spacing of the scale on the y -axis (or x -axis) is proportional to the logarithm of the number, not the number itself. It is equivalent to converting the y values (or x values) to their log, and plotting the data on linear scales. A log–log plot uses the logarithmic scale for both axes, and hence is not a semi-log plot.
Arrhenius plot. In chemical kinetics, an Arrhenius plot displays the logarithm of a reaction rate constant, ( , ordinate axis) plotted against reciprocal of the temperature ( , abscissa). [1] Arrhenius plots are often used to analyze the effect of temperature on the rates of chemical reactions. For a single rate-limited thermally activated ...
Fold change. Fold change is a measure describing how much a quantity changes between an original and a subsequent measurement. It is defined as the ratio between the two quantities; for quantities A and B the fold change of B with respect to A is B / A. In other words, a change from 30 to 60 is defined as a fold-change of 2.
This last form of the Hill equation is advantageous because a plot of versus [] yields a linear plot, which is called a Hill plot. [7] [8] Because the slope of a Hill plot is equal to the Hill coefficient for the biochemical interaction, the slope is denoted by . A slope greater than one thus indicates positively cooperative binding ...
Tafel plot for an anodic process (oxidation) The Tafel equation is an equation in electrochemical kinetics relating the rate of an electrochemical reaction to the overpotential. [1] The Tafel equation was first deduced experimentally and was later shown to have a theoretical justification. The equation is named after Swiss chemist Julius Tafel.
The Van 't Hoff equation relates the change in the equilibrium constant, Keq, of a chemical reaction to the change in temperature, T, given the standard enthalpy change, ΔrH⊖, for the process. The subscript means "reaction" and the superscript means "standard". It was proposed by Dutch chemist Jacobus Henricus van 't Hoff in 1884 in his book ...