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Easily use consensus sequences from the Project Window as a reference sequence for NGS alignments for hybrid sequencing projects.
New Batch Revert Trim Ends command.
The Assemble by Name assembly mode enables researchers unprecedented control and throughput when assembling large amounts of sample data from different sources simultaneously.
Sequence Editing
Sequencher gives you the DNA sequence editing tools you need to know that a sequence is absolutely correct. You can look at your chromatogram data one sequence at a time or view multiple aligned chromatograms in both forward and reverse orientations.
You can do BLAST searches in a Connections Session for individual sequences. Channels can be set up to search the NCBI databases with different parameters or databases used on each channel. Local-BLAST channels can be set up to search databases on your machine. You can also set up a Primer-BLAST channel to design primers over a region of interest and send those primer sequences to your Sequencher product. The primer sequences will have colored bases and the primer feature applied to them. The Schematic shows the results from multiple channels in a single window to allow you to compare the results from different runs.
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