This FAQ covers use of WAVEMAKER™ Software Version 4.0 and its features. It
does not address known bugs or workarounds for known bugs at this time.
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Project and Sample Set Up |
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Q. |
How do I use an existing project as a template for a new
project? |
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A. |
Open the project in WAVEMAKER Software and then select the Clear
Results button on the toolbar. A message will warn you that you are removing
results from the project. Press OK. Do not select the Save icon or use
the File | Save command or the old project will be overwritten. Select
the Save As command from the File menu and enter a new name before
selecting OK. |
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Q. |
How do I specify a set of default gradient parameters for new
samples? |
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A. |
There are three sets of default gradient parameters used for new samples.
These are selected by 'Caution Level' and they are labeled Fast, Normal and
Cautious. The parameters associated with each caution level are determined from
the Gradient tab on the Project Options dialog. To change the defaults for your
project, enter the new values and press OK. Samples created from now on will
have the new defaults. Remember that the caution level selected when the Project
Options dialog is closed becomes the default caution level for new samples. To
use the defaults for all new projects, select the Save as Project Default box
before pressing the OK button. |
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Q. |
What is the best way to duplicate sample methods for large
numbers of samples? |
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A. |
This depends on how the individual samples differ. For screening of large
numbers of identical samples, i.e. mutation detection in the same fragment, a
single method can be created and saved to disk. This method can then be set for
a large number of samples by filling the Method Name column. The Sample Name can
be specified before filling with the Method. The Sample Name can also be filled.
See the on-line help and the user manual for more information about Sample Table
editing features. |
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Q. |
How do I work with samples in the Sample Table without using
the mouse? |
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A. |
Click on one of the cells in the Sample Table to give it the focus. You can
then move from cell to cell using the cursor (arrow) keys. When you move to a
drop-down list, a button with a down arrow appears. Pressing Alt + down arrow
drops the list and you can then select an item using the up and down arrows. To
select the entire row, press Shift + left or right arrow. To select a group of
rows, press Shift + up or down arrow. Pressing F2 will open the context menu for
copying and pasting or filling. See the on-line help or user manual for more
keyboard functions and tips on setting up samples. |
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Q. |
How do I determine which detectors are used if I have more
than one? |
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A. |
The Instrument Configuration dialog shows which detectors are physically on
the instrument. These settings should not be changed unless the detector is
actually disconnected. The Project Options dialog allows you to disable a
detector for the present project. The detector may be connected and powered up,
but data will not be collected from a disabled detector. It is possible to mix
samples using different detectors within a single project by changing the
individual sample settings on the Run Information page. Select the specific
sample in the Sample Table and switch to the Run Information page to review the
settings. Press Apply after making changes. |
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Q. |
How can I set up a table of samples without using WAVEMAKER
Software? |
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A. |
The best way to set up a table of samples without being at the instrument is
to use the Desktop version of WAVEMAKER 4.0. The Desktop version creates the
same project files used in the System version. Otherwise, it is possible to copy
the Sample Table from WAVEMAKER Software into a spreadsheet program and make
changes in most fields. Care should be taken when changing the information in
the drop-down lists, i.e. Application Type, Sequence Name and Method Name. The
spreadsheet can be saved and used as a template for new tables by copying it
back into the Sample Table. |
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Q. |
Why do the changes I make in the gradient table revert to the
default gradient parameters? |
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A. |
Assuming you have checked the Edit Table box to allow changes to the gradient
table, you must press the Apply button to confirm the changes. If you uncheck
the Edit Table box before pressing Apply, the gradient parameters (gradient
duration, equilibration duration, etc.) will be reapplied to the
gradient. |
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Q. |
Why does the value I type in the Sample Table revert to the
previous value when I move the cursor? |
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A. |
It may not have been properly entered before the cursor was moved. Normally,
moving to another cell of the Sample Table confirms the entry. To ensure the
correct value, press the Enter key. |
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Instrument Configuration and Project Options |
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Q. |
I have two detectors and I want to disable one, but the
detector enabled box is gray and unchecked. |
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A. |
The Project Options determine if the detector enabled boxes on the Run
Information page can be changed. If a detector is disabled from the Project
Options dialog, that box will be grayed out in Run Information. If the method
originally had the detector enabled and then the project options are used to
disable the detector for new samples, the box will be checked and disabled.
Enable the detector in the Project Options and then uncheck the box on the Run
Information page before disabling the detector again. |
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Results Analysis |
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Q. |
How do I set the display scale for the charts on the Results
page? |
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A. |
The display scales for each chart can be set differently. To change the
default values, right-click on the chart and select Chart... to open the
Chart Options dialog. Select the Axes tab and enter the values. Check the
Save As Default box and press OK. The defaults will be used for all
projects. Be aware that the Autoscale to Data option on the Results
Options dialog overrides the axes defaults if it is checked. |
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Q. |
Why do I get both sublists in my report when I have only one
of them shown on the Results page? |
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A. |
If a sublist has any data loaded, it will be added to the Sublist Reports
whether it is shown on the Results page or not. To remove it from the reports,
close the Print Reports dialog and clear all the data from the other sublist
before returning to print the reports. |
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Q. |
How can I add more information to the chart display on the
Results page? |
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A. |
Both a chart title and comments for each result trace are available. To add a
chart title, right-click on the display to open the context menu and select
Chart.... The Chart Options dialog will open and the chart title can be
entered on the Chart tab. To add comments for each trace, type the text into the
Comment field in the Results grid. The Comments field may be hidden until you
scroll the grid to the left. The comments can be used in place of the sample
name when the chart legend is enabled. Open the Chart Options dialog and select
Comments instead of Sample Name, check the box to show the legend and press
OK. |
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Q. |
Why doesn't the Results page update for the sample that just
finished? |
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A. |
If one of the dialogs, such as the Project Options dialog, is still open when
an injection is completed, the results for that sample will not be added to the
Results page until the dialog is closed. It is recommended that the instrument
configuration and project options be reviewed and changes made before starting
to run samples. |
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Fragment Collection |
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Q. |
How do I save changes to a fragment collection table after
editing it? |
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A. |
Saving the project also saves the fragment collection job file. The job file
contains all of the collection tables and all of the result tables for the
associated project. |
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Q. |
How do I remove a single line from the fragment collection
table? |
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A. |
Select the line using the mouse and press the Delete key. If the line was
created with one of the multi-vial modes, the following vials will be renumbered
but the other settings will be unchanged. |
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Q. |
Why isn't a collection event added to the table even though I
have the markers placed correctly? |
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A. |
The data trace in the chart will have a blue highlight between the markers
when WAVEMAKER Software determines that the region can be collected using the
event parameters. If a blue highlight is not visible, the event will not be
added to the table. For Threshold detection, make sure the threshold line is
below the region to collect. For Peak, Leading and Trailing edge detection,
check the slope value selected. The value may be too high for the desired peak.
Press Update Chart after changing the value. |
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File Storage and Archiving |
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Q. |
Why can't I / WAVEMAKER 4.0 find my sequence files? |
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A. |
The location of the sequence file depends on where the project file has been
saved. If the project file has never been saved, a new sequence entered into
WAVEMAKER Software is saved into the Sequences folder under the WAVEMAKER 4.0
folder by default. If the project has been loaded first from disk, the new
sequence file is kept in memory and then saved with the project file the next
time the project is saved. Note that when the project is saved, any sequences
opened into the project from other folders are also saved to the project
location. |
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Q. |
Why do sequences I enter and save in the project disappear
when I save the project and reload it? |
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A. |
A sample must be completely specified for it to be saved into the project. At
minimum, an application type must also be set after the sequence is entered for
the sample to be complete. If only a sequence is entered for the sample row, it
will be cleared when the project is reloaded. The new sequence file will still
be saved with the project when the project is saved, but it will not be added to
the Sequence File drop-down list when the project is reloaded unless the sample
is completed. The sequence can still be opened into the project for later use
and it will then be added to the Sequence File list. |
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Q. |
Why can't I find a method I saved to the disk? |
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A. |
Methods are saved to the same folder where the current project file is
located. If a new project file has not been saved, the method will be saved to
the location of the last project file opened in WAVEMAKER 4.0. This behavior is
provided to make it easier to keep methods and projects for a specific
application together. To save the method in another location, select the desired
folder while using the Save Method dialog or save the new project to the desired
folder before saving the method. |
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Q. |
When I save methods to disk, they don't appear in the
drop-down method list on the Sample Table? |
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A. |
Methods are saved to the same folder where the project file is located by
default. If the project file has not been saved, the method will be saved to the
last project file opened in WAVEMAKER 4.0. The method can be saved to another
location by selecting the desired folder in the Save Method dialog. If the
method is saved to a location other than the default folder, it will not appear
in the Method Name list on the Sample Table or in the View Methods dialog as
these tools only look in the default location. Open the method from the File
menu to copy it to the default location and bring it into the
project. |
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Q. |
When I open an archived project, I see messages about
Sequences/Methods not being found. Why? |
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A. |
When a project has been archived or moved to a new location, method and
sequence files used in the project should be archived to the same location also.
When a project is loaded, it is assumed that any saved methods have been saved
with the project. Sequence files can be located either with the project or
loaded from the Sequences folder in the WAVEMAKER 4.0 folder. Transgenomic, Inc.
recommends that the project file be saved in the Application Folder used for the
project. The project and its associated methods can be more easily archived this
way. |
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Q. |
I have a set of sequences I want to start all my projects
with. How do I set this up? |
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A. |
Place the sequences into the Sequences folder under the WAVEMAKER 4.0 folder
and they will be added to the Sequence File list for all new projects
automatically. Note that if the project files are saved to different locations,
the complete set of sequences will also be saved with the project. This can
result in a large number of duplicate copies unless the projects are being saved
into the same folder. |
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Q. |
I have a set of saved methods I want to start all my projects
with. How do I set this up? |
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A. |
This can be done if projects are kept in a single folder. Place the method
files in the folder and they will be added to the Method Name list for all new
projects automatically. If the methods do not appear in the Method Name list,
open a project from the folder before pressing New Project. Transgenomic, Inc.
recommends that the project file be saved in the Application Folder used for the
project. The project and its associated methods can be more easily archived this
way. |
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Other Features |
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Q. |
When I'm using the Speed Plate to set up samples, how can I
tell which vial I have selected? |
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A. |
Select any vial on the plate diagram and the vial position will be indicated
in the status bar at the lower left. The format is row & column: vial
number. |
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Q. |
Why does the Estimated Run Time fluctuate when samples are
running? |
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A. |
The Estimated Run Time is adjusted as samples are run depending on the type
of sample and options such as equilibration, etc. |