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How to use DNA Baser Assembler
Part 3

 

How to assemble using a reference sequence

 

 

Level: beginner
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This tutorial will show you how to create contigs by assembling two chromatogram files to a reference sequence files.

 

DNA Baser Assembler uses the reference sequence to:


  - give the contig orientation
  - crop the contig

 

The reference sequence is not used for calculating the consensus sequence of the contig.

 

 

Starting the alignment process:


1. Open DNA Baser Assembler by clicking its icon on your desktop. When DNA Baser Assembler starts, the Project Manager should be opened by default. Navigate to the folder where your files are.

contig assembly software

 

2. Choose a name for this current project. DNA Baser Assembler will automatically choose a name for you but you can change it. Use this box to choose/change project's name: DNA chromatogram assembly

 

3. Next step is to choose a reference sequence. Drag and drop the desired sequence file in this panel: DNA chromatogram assembly.
The check box must be activated in order to assemble using a reference sequence.

 

4. Select the two or more files that are going to be assembled by adding them to the JOB LIST. DNA Baser supports SCF, ABI, FASTA and SEQ.

You can add files to the Job List in several ways:

-use the sequence assembly software button to add selected file/files to the Job List.
-use the DNA trace assembly button to add all files to the Job List.
-using your mouse, drag and drop files one by one from File List to the Job List.
If you want to remove files from the Job List, than use chromatogram assembly button.


5. The final step is to press the START chromatogram assembly button. In this moment, DNA Baser Assembler should begin the assembling process.

dna assembly software If something is wrong, the START button will be disabled:sequence assembly software

 

This can be caused by:
   - less than 2 files in the Job List
   - invalid combinations of file types in the Job List
   - one or more files in the Job List are invalid or it has been removed from your computer's hard disk meanwhile.


6. After the sequence assembly process, you can check the log window:

 

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7. The reference sequence will be placed in the contig grid (click here to read more about the contig grid) on the first position and it will have a light-pink background.

 

assembly to reference

 

Read the next Next chapter tutorial to find out how to assemble using the batch mode. If you have any questions, don't hesitate to write an email to us or to use our forum for support.

 

Note: Different file types can be mixed together. For example you can assemble ABI, SCF and FASTA sequences together.

 

DNA trace assembly
DNA contig assembly