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When you check this, peaks detected in any region that you select in the
Chromatogram Display Window are automatically added to the peak table.
The Fill Peak Table window is nearly identical to the Peak Table window, except
that you may click on any peak displayed in the Chromatogram Display Window
to add an entry into the table. A default name and peak parameters are entered
with the retention time of the selected peak. Click on the peaks of interest in the
display, zooming and scrolling if necessary to bring the peaks into view. After all
peaks have been added, click on the Save button.
Interactive Editing of Timed Events
Certain integration parameters can be set to affect only portions of the
chromatogram. This is useful to account for changes in the chromatographic
signal during the course of the run, or to better integrate partially fused peaks or
peaks that occur on a drifting baseline.
These timed integration events can be edited from the Time Events window
displayed from the Edit Method menu, or they can be graphically placed on the
chromatogram display. Peak table entries can also be graphically placed on the
chromatogram using the same technique. Time events that are added to the
chromatogram take effect when you perform a reintegration.
The Visual Method Editing Window is displayed below the chromatogram.
Events that have already taken effect (by reintegrating the chromatogram) are
displayed above the chromatogram trace.
Double-click on a marker to see the entire event table.
Event names and values are shown when you move the mouse over the event
marker.
Peak table entries are displayed as yellow boxes. Double-clicking on the marker
displays the peak table.
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