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Deleting bases in a sequence
These is a small difference between deleting bases in a chromatogram or in the contig: deleting a base from a sequence will simply remove that base. However, deleting a base from contig will replace that base with a GAP. This is necessary in order to keep the contig synchronized with the input sequences.
Deleting a base The delete functions can be accessed in different ways:
Attention: [Notes below applies only if you edit bases in the assembly window] In Assembly window, deleting bases from one of the assembled chromatograms will break the synchronization between that chromatogram and rest of the assembled chromatograms. DNA Baser will show a one-time-warning about this issue. In addition, by deleting a base from one of the assembled chromatograms, you force DNA Baser to recalculate the contig. This means that all editing that you have done in contig (staring at the current deletion point and up to the end of the contig) will be lost. Because of this, we recommend you do make any deletion you want at the beginning and only when you are done deleting bases, you can proceed editing the contig. To stay away from troubles, please avoid deleting bases, in order to keep the synchronization between sequences. Instead of deleting a base, you may want to replace it with a GAP.
Hints: * You can delete a single base (the base under the cursor) or all selected bases. * To edit a single sequence, double click that sequence in Project Manager to load it. Multiple sequences can also be easily edited in the Assembly window. * In Assembly window, you may want to replace a base with a GAP instead of deleting it. EXAMPLE - Deleting 20 bases at once:
Related topics:
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