Zooming

Zooming in and out on the timeline is one of the most fundamental skills needed to master ACID. Fortunately, zooming is very easy, especially if you have a mouse with a wheel button. 

A much closer look at the same project. Zooming in can allow editing at the millisecond level. 

Zooming out using the Vertical Zoom/ScroU bar makes the tracks shorter and allows more tracks to be viewed at the same time. 

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An invaluable glossary of over 300 words, from aberration to zoom by way of crippled lead-frog tests and output bus drivers . 

The zoom optics between the image intensifier and the video camera gives the freedom to magnify details of the image for more detailed inspection. 

The analyze mode display is similar to the scan mode display used online. Analyze mode includes functions for evaluation of data, e. g. markers, measure functions, zoom function and selection of cross-section views. In addition, A-scan data can be reconstructed into images and displayed. 

Figure 5 Echo evaluation with TCG, zoomed screen with the USLT 2000...

Figure Bl.19.9. Plasmid DNA (pUClS) on mica imaged by STM at high resolution. The inset is a cut-out of a zoomed-in image taken inunediately after the overview. (Taken from [42], figure 2.)...

Fig. 2. Left Time average (over T = 200ps) of the molecular length of Butane versus discretization stepsize r for the Verlet discretization. Right Zoom of the asymptotic domain (r < 10 fs) and quadratic fit.

Fig. 3. MD simulation of a polymer chain of 100 CH2 groups due to [10], The dynamics of the distance between two CHj-groups ( 12 and 36). The series of plots illustrates the oscillations of the distance at time scales increasing by a zoom factor of 10 at each level.

In order to represent 3D molecular models it is necessary to supply structure files with 3D information (e.g., pdb, xyz, df, mol, etc.. If structures from a structure editor are used directly, the files do not normally include 3D data. Indusion of such data can be achieved only via 3D structure generators, force-field calculations, etc. 3D structures can then be represented in various display modes, e.g., wire frame, balls and sticks, space-filling (see Section 2.11). Proteins are visualized by various representations of helices, / -strains, or tertiary structures. An additional feature is the ability to color the atoms according to subunits, temperature, or chain types. During all such operations the molecule can be interactively moved, rotated, or zoomed by the user. 

To perform a vibrational analysis, choose Vibrationson the Compute menu to invoke a vibrational analysis calculation, and then choose Vibrational Dectrum to visualize the results. The Vibrational Spectrum dialog box displays all vibrational frequencies and a simulated infrared spectrum. You can zoom and pan in the spectrum and pick normal modes for display, using vectors (using the Rendering dialog box from Display/Rendering menu item) and/or an im ation. 

In 1982, the European Space Agency s Information Retrieval Service (ESA/IRS) introduced the ZOOM command, providing users with a mechanism to analy2e retrieved sets. In 1984, service at a baud rate of 2400 was made available by Tymnet and Telenet for pubHc access to on-line databases. In 1985, the first commercial CD-ROM drives for personal computers became available, along with the first commercial CD-ROM databases. 

Conditions CDCI3, 25 °C, 500 MHz (H), 125 MHz ( C). (a) //NMR spectrum and HH COSY plot of ethyl groups (b) HC HSQC plot with inserted zoomed section of ethyl groups ... 

The Important Sequence Model module does sensitivity studies and importance rankings for about a thousand highest frequency sequences. The analyst zooms to the most frequent plant damage category, to the most frequent sequences in that category, to the most important top event, to the most important split fraction, and to the most important cutsets. If sensitivity analysis is needed on the model as a whole, a menu option, "CLONE a Model," makes a copy of the model, c hange,s are made, and results compared. 

Fig. 4-16. Decision tree built by MLC++ from the analysis of 3000 solutes resolved on 18 commercially available CSPs. The magnifying glass shows the region zoomed in Fig. 4-17.

As the entire tree is complex and cannot be clearly displayed in one screen, we report in Fig. 4-17 an expanded (zoomed) fraction of the nonaromatic population set of the tree. 

Fig. 4-17. Zoomed picture of the decision tree in the nonaromatic region. (0) indicates no (1) indicates yes . (A) for any atom except hydrogen. ( ) indicates that the bond is part of a ring, and ( ) bond is part of a chain. CC(C)(C)A for tBu.

Figure 8-5. Transmission difference spectra of m-LPPP films at 7=77 K excited at 3.2 eV for various pump-probe delays. The inset zooms out the low energy region for 0 ps (solid line) and 400 ps (dashed line) delay. Doping induced absorption (D1A) data are also shown for comparison (from Ref. (251 with permission).

In the kinetic model of gases, we picture the molecules as widely separated for most of the time and in ceaseless random motion. They zoom from place to place, always in straight lines, changing direction only when they collide with a wall of the container or another molecule. The collisions change the speed and direction of the molecules, just like balls in a three-dimensional cosmic game of pool. 

I This result means that nitrogen molecules are zooming about your head at about 1140 miles per hour. 

Once plotted, a new menu bar appears with plot options. The plot can be displayed as points, connected, or as a bar chart. The data can be presented on linear or log axes, with or without grid. Text can be placed on the display in a variety of sizes and types. Lines or arrows can be drawn or areas filled. The user can edit all axis labels and titles if desired. Re-scaling is accomplished by means of the shrink and zoom options or by entering exact scale limits. Multiple curves can be annotated with keyed symbols. Plot coordinates are displayed in real time as the operator moves the mouse over the plot. 

Once creation of the PV A database is complete, optimized probabilities may be calculated for the experimental spectrum at hand. Since the iterative procedure is restricted to a 2048 data point region, zoom cursors are displayed and set by the user until this condition is satisfied. In this case, the methylene region was selected and an initial guess for the Bernoullian probability (Pr=0.5) and linewidth (13.0Hz) were given. Optimized values for the probability and linewidth were Pr=0.52 and 12.8Hz, respectively. 

Figure 4 shows zoomed regions of the experimental and simulated spectra. The methine region was simulated separately using the same optimized probability but with a linewidth of 8.0 Hz. At this point the user may wish to use the spectral manipulation options (overlay, subtraction, etc.), repeat the calculation, or do further simulations. 

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