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Sequencher 4.8 User Manual--PC - Bioinformatics and Biological ...

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Note: When a sequence becomes part of a contig the data are automatically recorded as<br />

experimental data if they have not previously been stored in that form.<br />

Once a version of the sequence has been recorded as experimental data, all future changes<br />

are considered to be “edits” to it. As a data quality tool, all such edits can be marked in<br />

color <strong>and</strong> displayed in Bold Magenta or lower-case text. This feature is invoked in the<br />

View menu under the Base Edits As comm<strong>and</strong>. The default is set to Bold Magenta but<br />

you can also choose Not Highlighted or bOLD & cASE cHANGE.<br />

Resetting a baseline<br />

If you decide that some of the original data was incorrect (perhaps a simple typing error<br />

that has been corrected in the “edited” version of the sequence), go to the “Experimental<br />

Data” version of the sequence by clicking the Show Experimental button <strong>and</strong> then click<br />

the New Baseline button.<br />

Note: Setting a new baseline for a sequence resets all of the bases to a not-yet-edited<br />

state. None of the bases that were edited will appear in Bold Magenta letters.<br />

Viewing experimental data<br />

After you enter a new sequence, <strong>Sequencher</strong> archives a copy that is “locked” (not<br />

editable). In the course of assembling your data, you may make a great number of edits<br />

to any particular sequence. This locked version enables you always to refer back to<br />

the sequence as it was originally entered. To see the Experimental Data version of the<br />

sequence click the Show Experimental button in the Sequence Editor button bar.<br />

Reverting to experimental data<br />

If you edit a sequence incorrectly, you can delete all the changes to that sequence <strong>and</strong> go<br />

back to the archived baseline. To do so, open the Sequence Editor . Then choose Revert<br />

To Experimental Data from the Sequence menu.<br />

If you edit a contig incorrectly, you can delete all the changes to an individual sequence<br />

<strong>and</strong> go back to the archived baseline. To do so, open the contig editor. Select the sequence<br />

by clicking on its icon which can be found on the left h<strong>and</strong> side of the contig editor.<br />

You can now remove the sequence from the contig by using the Remove Selected<br />

Sequences… from the Contig menu. Then choose Revert To Experimental Data from<br />

the Sequence menu. You can then reselect the fragments <strong>and</strong> rebuild the contig.<br />

Viewing experimental data for Chromatograms<br />

If your data came from an automated sequencer, click the button labeled Show<br />

Chromatogram to view the experimental data of a sequence. This will display the<br />

original trace data. <strong>Sequencher</strong> allows you to scroll either vertically (the default) or<br />

horizontally. To change the scroll orientation, click the appropriate button in the left<br />

bottom corner of the fragment chromatogram window. (See Chapter 15 “Chromatograms”<br />

for more information.)<br />

SEQUENCHER <strong>4.8</strong> <strong>User</strong> <strong>Manual</strong> for Windows © 1991 - 2007 Gene Codes Corporation, Inc. All rights reserved.<br />

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