ANALYZE menu

GENERAL NOTES ON ANALYSIS PROCEDURES:
To select a data block:
 Use the normal Macintosh clickholdanddrag method, with the cursor within the plot area.
 Move the cursor to the beginning point on the plot area and click once, then repeat this procedure for the end point (which may be on either side of the beginning point).
 Alternately, blocks of predefined duration can be selected with single clicks (BLOCK WIDTH option, below).
Blocks can include multiple screens. In ACTIVE SCREEN mode, mark the start of the block, then shift screens as necessary until the end of the block can be marked.
This example of a block window shows the upper and lower limits of the data within the block. This particular block (being analyzed with the Integrate option) also shows:
MORE BLOCK HANDLING AND ANALYSIS TOOLS:
*If you want to adjust the font size or the time delay for the 'Tool Tips' windows that show channel labels, and you feel comfortable entering text commands directly into MacOS, activate Terminal (Utilities folder, in Applications). Then:
To change font size to 14 points (or any value you like), type this (followed by RETURN):
defaults write g NSToolTipsFontSize int 14To change the activation delay to 20 ms (or any value you like), type this (followed by RETURN):
defaults write g NSInitialToolTipDelay int 20
If no data block is selected you can perform the following two operations (as well as Fast Fourier transforms):
To select points for analysis, move the cursor to the point of interest in the plot area and click once. Then move to the next point and repeat.
NOTE: this operation DOES NOT highlight the results window title when active, as can be seen in the example above.
To get the integrated total for a rate function, such as oxygen consumption, make sure the correct rate unit is selected (i.e., 'per min' if the units are ml/min or 'per hour' if the units are ml/hour). A more sophisticated integration mode is available in the INTEGRATE BLOCK option.
Use the 'limits' buttons to restrict analysis to a subsection of the block. Click the right or left limit button, then use the cursor to select the limits in the block window.
The 'scale' button toggles scaling of the results (see SCALE RESULTS, below). The 'Store' button in this and other analysis mode windows allows you to directly transfer the current mean for use as a scaling factor. When you click 'Store', the scaling factors window appears. Click on any channel's "*" or "÷" button, and the current mean will appear in the first edit field (the multiplication or division factor) for that channel.
The 'select,' '≥' and '≤' buttons at the bottom of the window let you get basic statistics for a subset of the block, within the defined numeric limits. Note that there must be at least 3 data points within the subset limits, or the program will issue a warning buzz, turn off the '≥' and '≤' buttons, and default to the previous basic statistics results.
The 'distribution' button produces a small histogram (bar graph) of frequency distribution in a small moveable window. You can use the '(big)' button to produce a much larger and more detailed histogram, with control over the number of bins and bin width (see below). If the file has more than one channel, you can click on buttons for different channels and get those means (you can also use the keyboard to select channels). With an option in the PREFERENCES menu, you can have different histogram windows for each channel, or use the same small window for all channels.
Allow you to enter an interval (in seconds) and LabAnalyst will search within the selected block for either the highest or lowest continuous average over that interval, or the most level or most variable region within the block. In this example, the scan interval (86,400 seconds) is an entire day.
Activating the 'reuse this interval' button in the interval selection window will bypass the interval selection routine during subsequent uses of these analyses (such as when using the AUTOREPEAT option for new blocks).
You can restrict the analysis to specific ranges of data using the 'Exclude if' options. In the example, data with values less than 0.5 or greater than 21.12 are ignored during calculations.
For the MOST LEVEL option, the 'most level' region is the interval in which the sum of absolute differences from the interval mean (i.e., the sum of X_{}i  meanX, or pointtopoint variance) is lowest. Note that this is not necessarily the interval with the lowest slope, although this usually turns out to be the case.
For the MOST VARIABLE option, you can select to search either for the region with maximum overall slope or the region with maximum pointtopoint variance.
When your interval selection is complete, click the 'interval OK' button and the program will find the appropriate interval and display the results in the next window, shown below.
After calculations, the maximal, minimal, or most level area is shown as a colorinverted rectangle on the block window.
As for BASIC STATS, you can switch to other channels, but in the default mode the interval boundaries remain constant  i.e., the same beginning and ending points as on the initially scanned channel are used for other channels. This sounds confusing but it allows you to scan for the period of, say, lowest VO_{2} and then get the temperature, CO_{2}, etc. for that specific period.
Alternately, you can activate the 'rescan new channels' button to force a rescan of each new channel selected.
Two other considerations:
When using the MINIMUM VALUE... and MAXIMUM VALUE... functions, a button labeled 'C.V.R. data...' is available. This stands for Constant Volume Respirometry, and it opens a window that lets you set up the variables needed to compute O_{2} or CO_{2} exchange in a closed system. In constant volume respirometry (or 'closed system' respirometry), the organism is placed in a sealed chamber, and over time its respiration changes the gas concentrations in the chamber. You measure rates of gas exchange by determining gas concentrations (O_{2} and/or CO_{2} ) at the start and end of a period of measurement, and then using the cumulative difference in concentrations and the elapsed time to compute the average rate of change.
The most straightforward way to handle constant volume calculations with LabHelper and LabAnalyst is as follows: First, collect samples of 'initial' and 'final' gas from the animal chamber(s) and inject them through a gas analyzer while continually recording the concentration (in %) with LabHelper. Between injections, flush the analyzer with reference gas (or fluid). You should get a data file with a series of 'peaks', one for each injection of 'final' gas (or fluid). Next, in LabAnalyst, use the baseline function to set the 'initial' values at zero. The 'final' values now show the % change during the measurement period. These peaks are what you analyze with the C.V.R. data... option. For each peak, find the maximum deflection from baseline with the MAXUMUM VALUE option, and then switch to C.V.R. data....
Note that this option assumes that the data being analyzed are in units of % gas concentration and that baseline has already been corrected. You need to specify the gas type, the chamber volume, the elapsed time, the chamber temperature, the barometric pressure, the initial relative humidity in the chamber (if the gas contains water vapor), the initial concentrations of O_{2} and CO_{2} (FiO2 and FiCO2), and the respiratory exchange ratio (RQ). You also need to specify whether or not CO_{2} is absorbed prior to oxygen analysis ('excurrent CO2' buttons). When done, click the 'Selection OK' button.
When C.V.R. data... is activated, the results window (example on the right) shows gas exchange rates in units of ml/min  but note that only the mean value is computed as gas exchange (the SD, SE, etc. are shown in their original units). To switch off the C.V.R. calculations, click the 'C.V.R. data...' button. Note that this is a “quick and dirty” CVR estimate; a more versatile CVR calculator is in the SPECIAL menu.
You can avoid using interpolated data in these operations if you select the 'Avoid interpolated data' option in the ANALYSIS UTILITIES submenu (bottom of the ANALYSIS menu).
There is a choice of time units (seconds, minutes, hours, days, none) and baseline values. The baseline for integration can be set at zero, the initial value of the block, the final value of the block, a userspecified value, or a proportional linear correction between initial and final block values. Because of the different baseline options, this operation is considerably more versatile than the integration feature including in BASIC STATS, MINIMUM, MAXIMUM, and LEVEL.
In this example, the block is integrated using the zero baseline option with the time unit set as minutes. Note that the start, end, and proportional options apply to the block defined with the left and right limit functions.
Keep in mind that you need to pick the time unit that matches the rate unit used in the channel being analyzed, or the results will not be valid. If you are using a rate unit for which a matching time unit is not available, you will need to adjust the results manually. For example, if your data are in units of Kilojoules/day, you will need to divide the results by the factorial difference between days and whatever unit you select. To continue with this example, if you set the units to 'hours' and your data are in KJ/day, you must divide the results by 24 (since there are 24 hours per day). Similarly, if you set the units to 'minutes', you would need to divide by the number of minutes per day (1440). This can be done conveniently using the 'Store' and 'Scale' buttons.
If you select the "∑ plot" option (button in the bottom row), the computer generates a plot of the integrated values over time. This plot will change whenever a new channel, right or left limit, or baseline option is selected.
Additional considerations:
In the default mode the program will use all the data within the block. Alternately, 'filtering' is possible through cursor selection of minimum peak and valley values ('triggers') in the block window. Click the 'use cursor' button and move the cursor to the block window. A horizontal line will track the cursor's movement and a readout in the Results window will show the height of the cursor. Click once to select a peak (done first) or valley trigger. After selection, peak triggers are shown as pink lines, and valley triggers are green lines. The postpeak trigger value (default zero) is the number of cases the program 'skips' after finding a peak. This option can be useful when analyzing noisy files.
A typical results window is shown at right, above. Note that in this example the number of periods and amplitudes is correctly matched. The program beeps and prints a warning if no periodicity is found, if no amplitudes are found, or if the number of amplitudes does not equal the number of cycles +1 (indicating that some peaks were not associated with definable valleys, so the frequency or amplitude may be incorrect). The mean values for both peaks and valleys are also shown.
NOTE: The waveform algorithms are easily confused by noise (because of the way peaks and valleys are defined). If you are only interested in frequency, it is reasonably safe to reduce noise by smoothing data prior to analysis. However, smoothing reduces peak amplitudes (in some cases very dramatically), so it must be used with caution if you need peak height data. Smoothing is least damaging if peaks are 'rounded' and contain many more points than the smoothing interval. If necessary, use PAIRS DIFFERENCE to obtain peak heights, then obtain frequency data after smoothing.
The 'wave shape data' button opens a window with statistical information on the waveform's rise and decay times.
Rise time (the elapsed time from a valley to a subsequent peak) is shown in blue; decay time (the elapsed time from a peak to a subsequent valley) is shown in red. The small triangles indicate the means while the bars show the distributions.
If the data contain more than 10 peaks, additional analyses are available from the Peak and interval histograms button, which produces histograms of peak height (shown as the absolute value), wave amplitude (valley to peak) and interpeak interval (essentially the wavelength calculated on a peaktopeak basis), selected with a popup menu. Another popup menu lets you select the number of bars in the histogram. An example is shown below.
The save data button stores a text file of the histogram values, the print graph button sends the data to a printer, and the squareroot Y button shows the count as a squareroot, which better shows bars with low counts.
BASIC TIME SERIES... This option displays time series data in graphical form. Time series analysis examines data for many kinds of temporal relationships  basically, does sample value at a particular time ( T ) predict sample value at some later time ( T + z)? A graphical display is useful for determining if there are periodicities within the data, and (if periodicities exist) if the waveforms are symmetrical. When this option is selected, LabAnalyst opens a window containing edit fields for the Start Lag (the initial time increment between samples) and the Time Step (the time increment added for each successive plot). Defaults are a start lag of 0 and a time step of 1 sample. Edit as desired. There are two plotting options: Use the 'Plot time series' button to generate 18 scatterplots. For each, the sample value (X  coordinate) is plotted against the sample value at a fixed time increment in the future (Y coordinate):
In each plot the time increment is equal to the start lag plus the sum of the cumulative time steps (i.e., start lag + time step X plot number). The increment value is shown at the top of each plot. If there is no temporal predictability, the point distribution will be random. However, if temporal patterns exist, the distribution of points will be nonrandom, and the shape of the distribution will indicate the degree of symmetry and the scatter will indicate the degree of randomness or 'noise'. You can replot with different start lags and time step increments. Click the 'Print plots' button for hardcopy output. Note that 24, not 18, time steps are plotted, and that you cannot select this button until data have been plotted on the screen.
• Use the 'periodicity test… ' button to generate a summarized periodicity test for 50, 100, 200, or more stepped time intervals (NOTE: the interval selection buttons are only available if there are sufficient points within the block). For 200 or fewer steps, results are shown as a bar graph; for more steps a line plot is drawn. This is the setup screen for generating a periodicity test:
Output from a typical periodicity test looks like this:
This example shows a 750step plot. Correlations with negative slopes are plotted below the zero line. Bar (or line) heights are a relative index of how value at time ( T ) predicts value at time ( T + time step). The tallest bar (red on color screens) is the interval with highest predictability. Click the 'Show Other Peaks Where...' button to display only those time correlations with r^{2} higher than a specified value. Click the 'Print' button for hardcopy output; click the 'Quit' button, another window, or the close box to return to the analysis page.
STEPPED SAMPLING... This routine computes, plots, and saves sequentially sampled data at userset intervals; among other uses, this helps determine the degree to which data sampled at one time are correlated to data sampled at different times (i.e., autocorrelation). For example, if you wanted to compute a relationship between (say) voluntary running speed and metabolism from a file containing many different running speeds, you would need to obtain your measurements at large enough intervals so that there was no autocorrelation between measurements. The intuitive expectation is that successive measurements obtained at very short intervals will closely resemble each other, but eventually become independent as the interval between measurements increases. The goal would be to use an intermeasurement interval large enough to be sure that autocorrelation ('pseudoreplication') is minimal. The iterative sampling process starts at an initial point (a particular sample) in the file, then steps forwards and backwards by userdefined intervals (the 'skip' interval) and takes the mean, range, and SD of blocks of data of userset duration, symbolized as:

where  = skipped samples,  = blocks, and  is the initial point
This process is repeated until userdefined limits are reached, or the start of end of the data are reached. The initial point can be a userset sample number or the central point in a data block (for example, you could search for the highest point in a data file, use the 'set block' option, and then use the resulting block as the initial point). If a block is selected, the start and end points are set to the beginning and ending points of the block. The default value is 1/2 of the total number of samples. The control window looks like this:
When ready, click either the "deltat step plot" button or select a new channel to display results, as in the following example:
Results are plotted onscreen (blue for measurements later than the initial point, red for measurements earlier than the initial point, and gray for the mean value for both + and  values at a given interval).
The 'scatterplot' button shows an XY scatterplot of stepsampled data from any two of the available channels (it's only available if there are 2 or more channels in the file).
You can use the channel buttons to select up to 10 channels that can be analyzed and stored in a tabdelineated (Excel compatable) file with the "save as ASCII" button. Note that you can select more than 10 channels, but only results from the first 10 will be stored. If the file contains interpolated data as indicated with the standard interpolation markers "»" and "«", any stored values that were computed from interpolated data will be marked in the Excel file.
Complex 'summed' frequency data occur frequently in biology (and in other areas of science). For example, you might want to use an impedance converter to measure the heart rate in a small mammal, bird, or lizard. Unfortunately, in addition to heart rate, you will also pick up signals produced by breathing movements. Therefore the instrument output will contain a confusing summation of the combined effects of breathing and heart rate. It may also contain 'noise' from random or irregular events (such as muscle movement from minor postural adjustments).
The messylooking data shown at right are an example of such a waveform. Although it is obviously complex, a visual inspection suggests that it does contain some regularity. However, this periodicity is not readily studied with either the WAVEFORM or TIME SERIES operations. Fortunately, the FFT procedure can help find the important underlying components of this complex wave. In many cases it can detect basic cycles in a data set even if they are visually 'buried' by random noise.
After you select a block size, the program will show the block duration and then prompt you to go to the plot window and select the block to be analyzed. Do this by moving the cursor into the plot area, where it will outline a block of the size you selected. Fit the cursor block over the subset of data you wish to analyze and click the mouse once. This will select the desired FFT block.
Once the block is chosen, you can proceed transform it (Do FFT button), select another block size ( ‘∆ interval’ ), or exit. You may choose between showing a line or histogram plot of the results, and whether or not the results are smoothed.
After completing the FFT, the waveform's fundamental frequencies are shown graphically in the plot area. You can examine the details of this structure by moving the cursor over the plot; the fundamental frequencies that have been 'decomposed' from the original signal, and their amplitudes, are shown numerically as peaks in the results window.
In this example, the waveform from the first image (above) is seen to be composed of three discrete fundamental frequencies, which appear as the three sharp peaks in the plot area. The cursor is over one of the peaks, which has a frequency of .00566 Hz and a magnitude (useful for comparisons among peaks) of .13976 (these data are displayed in the results window). You have a choice of output units (frequency in Hz, kHz, etc.; period in sec, min, etc.)
After the transform is complete, you can expand or shrink the display, or smooth (or unsmooth) the data (the results in this example are smoothed).
FFT results are stored in channel zero (not normally used by LabAnalyst ); use the copy button to move them to a 'regular' data channel if you want to save them to disk (copying is only possible if the number of 'regular' channels is <40). Alternately, you can use the 'save FFT…' button to produce an Excelcompatable spreadsheet containing the frequency data (the time units will be saved in whatever frequency or period you have selected with the popup menu) and amplitudes.
Note that if you click the exit button, you are transferred to the plot area window in channel zero (which contains the FFT results). If you click the close box you are transferred back to the original data channel. If you chose the former, you can switch back to the regular channels by pushing the appropriate number key, or clicking the channel selection buttons in the upper right corner of the plot area. You cannot get back to the FFT results in channel zero except by rerunning the FFT procedure.
Note that if you start the FFT procedure while using the multichannel display mode, you'll be switched to singlechannel mode (using the current active channel) prior to the beginning of analyses. At the conclusion of the FFT calculations you'll be returned to multichannel mode IF you click the close box or (in FP versions) the plot area.
Two values of 'a' (the intercept) are given. One is based on the time change calculated from the start of the file (t=zero), and the other is based on the time change within the block, using the assumption that time zero is the start of the block.
You can use the 'predict values' option to calculate specific Y values as a function of time, or vice versa (this uses the intercept value calculated from the start of the block, not the start of the file). At present, this does not 'backconvert' from log to linear, so if your equation uses log time and log Y, you will need to convert your inputs to their log equivalents, and do the reverse for predicted values.
You can switch channels (for new calculations) with the usual selection buttons on the bottom of the results window. To change the time units, reselect the original channel.
You can also test the slope against any userdefined value with the 'test' button. The 'Residuals…' button draws a plot of the residuals from the regression; results  time, observed value, predicted value, and residual  can be saved to an Excelformat text file.
Some additional considerations:
The initial step in the regression procedure is to chose the type of unit conversions. Linear (leastsquares), semilog (log Y = a+b*X or Y = a+b*log X), and loglog (log Y = a + b*log X) regression models are available. However, some of the conversions will not be available if the data range includes zero or negative values (since one can't take the log of a negative number).
Next, you select the two channels to regress, using the window shown at right. The program won't let you attempt to regress a channel against itself, so you may have to do some fancy buttonclicking to get your channels selected.
After the 'selections OK' button is clicked, LabAnalyst performs the calculations and produces a scatterplot of the data points in the block window (x values versus y values), along with the regression line.
The numerical results are the same as for the SLOPE vs TIME option described above  except that only a single value of the intercept is shown.
You can test the slope against any userdefined value. Enter the slope into the edit field and click the 'test' button (very low probability values are shown as "<.00001").
The 'residuals' button will produce a scatterplot of residuals from the regression. 'Select new channels' lets you set up a new regression of different variables.
You can use the 'predict values' button to use the regression equation to predict X from a given Y, or vice versa:
Some additional considerations:
The program uses an iterative method to find the bestfit asymptote for a selected block of data, according to the simple model: Y = ln (asymptote  data). You can chose any number of iterations between 6 and 50. Using a lot of iterations might increase the accuracy of the estimate (this doesn't always occur), but will also increase the analysis time. In practice, you usually don't need to use more than 6 to 10 iterations for good accuracy. Note that if you give it 'messy' data that do not conform reasonably well to firstorder kinetics, the program may take a long time to produce an estimate (and that estimate may have fairly glaring errors).
After completing the analysis, LabAnalyst shows the asymptote, the coefficient of determination or C.D. (an estimate of the precision of the fit of the data to the model, and hence the precision of the estimated asymptote), the slope of the lntransformed data, the rate constant (the fraction of the change between a starting value and the asymptote that is completed during 1 time unit), and the time to complete a fraction of the total change between a starting value and the asymptote (values from 1% to 99% are selectable from a popup menu). You can use your choice of time units (seconds, minutes, hours, or days) for slopes and rate constants.
LabAnalyst also draws a goodnessoffit plot that illustrates how closely the model matches the data. Points are plotted in yellow as the log (base e) of the absolute difference between the model predictions and the data:
Y value = ln(abs(asymptote  data))
Individual points are shown only if the total number of points in the plot is less than 60. The line predicted by the model is shown in white. In this example (not the same as for the previous figure), the analysis contained 31 points ranging in value from about 31.1 to slightly less than 0, with a predicted asymptote of 0.05. If you are analyzing less than 200,000 points, you can also plot the residuals from this regression (example at right).
Some additional considerations:
After completing the analysis, several options are available. The 'Pick New Channels' button lets you change the X and Y variables. The 'Make New Chan From Polynomial' button (only available if the number of channels is less than 40) generates a new channel by applying the current polynomial equation to the data in the X channel  in other words, it computes and saves a new Y value for every sample in the X channel.
The 'Show All r^2' button helps you select the most appropriate degree for the polynomial equation. The predictive value of a polynomial always increases as the degree increases. However, the increase in accuracy usually plateaus, so it is reasonable to use the simplest equation consistent with good predictive power. When the 'Show All r^2' button is clicked, the program computes the r^{2} value for all degrees between 1 and 9, and then shows a bar graph of the results. [You can remove this plot by clicking the highlighted 'Ahow All r^2' button.]
In the example shown at right, there was little change in predictive power until the degree of the polynomial exceeded 3, and then little additional change until the degree reached 8 and 9 (you can select the color of bar graph plots in the Colors and lines option in the VIEW menu.)
Additional considerations:
An example time integration window is shown at right. The default minimum and maximum values are the lower and upper limits (respectively) of the data range in the block, which includes 100% of the data and results in a single event in each category. You can set new limits (as shown here) in three ways:
The right side of the window shows basic statistics for the durations of positive and negative events (mean, SD, range), and a histogram of these values. Only complete events (including both beginnings and endings) are shown here. You can elect to analyze only events longer than a minimum duration. The 'show all events' button forces the basic event counters to show all events, not just those longer than the minimum duration.
The 'save details' button makes a text file (Excel format) containing the polarity (positive or negative), start time, duration, and basic statistics (mean, SD, minimum, maximum) for each identified event. Some additional considerations include:
An example of selective integration is shown at right. The default minimum and maximum values are the lower and upper limits (respectively) of the data range in the block, which includes 100% of the data and results in a single event in each category. You can set new limits (as shown here) in three ways:
AUTOREPEAT R Toggles the autorepetition feature for analysis modes. When active, autorepeat mode repeats the last analysis used whenever a new block is selected. If you want to do something different, just pick the new analysis from the menu or from the buttons below the plot area.
BLOCK WIDTH... Allows automatic selection of blocks of userdefined duration with a single mouse click, instead of the normal method of clicking on both the start and end of the desired block (or clicking and dragging). In this mode, the cursor is contained within a box that 'frames' the block duration in the plot area. Position the cursor over the desired block and click once to select it. The default automatic block size is equivalent to 13 samples or 12 sample intervals (e.g., 60 seconds with a 5second sample interval). Any other block size can be selected, as long as it contains more than 2 samples and less than 1/4 of the file duration. In this example, a 5minute block duration (300 seconds) has been selected.
Return to the standard twoclick selection method with the 'Normal block selection' button.
SCALE RESULTS... Opens a window for entry of scaling factors that can be selectively applied to the results of several analysis operations with the 'scale' button (in the RESULTS window). These factors take the form: final value = (result x B) +A or final value = (result ÷ B) +A
Different A and B values can be applied to each channel, but you must enter the correct values in any channel you wish to scale (in other words, if you have scaling factors entered for channel 5, they apply only to channel 5 unless they are also entered in another channel of interest).
This example shows:
The 'Store' button in many of the analysis mode windows allows you to directly transfer the current results mean for use as a scaling factor. When you click the Store button, the scaling factors window appears. Click on any channel's "*" or "÷" button, and the current mean will appear in the first edit field (the multiplication or division factor) for that channel. CROSSCHANNEL SUBSET SELECTION Use this option to restrict analysis according to specific ranges or values of data in another channel. In the example shown here, data during the night are ignored (i.e., times between 18:00 and 06:00), as are data where temperature (Ta) is hotter than 65 or colder than 0.5. It is not used in the example, but restricting to single values is possble (using the '=' option), but this is very restrictive and is probably best suited to boolean data (zero or one, for example). If you use this option, make sure your restrictions leave SOME data available for analysis  this is especially important if you are setting restrictions on more than one channel.
If you use crosschannel subsets, a warning window will appear for analyses that 'pay attention' to subset settings. This example shows crosschannel selection is being used, and within the channel being analyzed, data with values less than 0.5 or greater than 21.12 are ignored.
DON'T USE INTERPOLATED DATA If this option is selected, the AVERAGE, MINIMUM VALUE, MAXIMUM VALUE, MOST LEVEL, MOST VARIABLE, SLOPE OVER TIME, and REGRESSION operations will not use interpolated data when scanning for desired values. Note that it does not matter which channel was interpolated: if this option is selected all data from any channel within interpolation boundaries will be rejected. Note that interpolation is determined from the standard interpolation markers: "»" indicates the start of interpolation and "«" indicates the end of interpolation. These are optionally set automatically in the Remove references and Interactive spike removal operations, or you can insert them manually from the 'markers' submenu in the VIEW menu. If you have selected this option and an analysis operation encounters interpolated data within the regions selected for analysis, this warning window is shown:
You will also notice that the number of cases shown in the 'Results' window is less than shown in the 'Block' window. The difference is the number of interpolated data points that were ignored during analysis.
BLOCK SHIFT RULES This opens a small window that lets you select how the shift block operations work: with or without overlap of one case. For example, if your block contains cases 200400 and you shift it right with overlap, the new block will contain cases 400600. If you use the default nonoverlap option, the new block will contain cases 401601.
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