DNA Baser Sequence Assembler will do all the work for you. It will:
- Automatically detect and trim low quality regions of your samples
- Automatically trim vector sequences
- Automatically correct the ambiguities in your contig
- Automatically save the project and the contig to disk
- With DNA Baser you will need literally 5 (five) seconds to go from unassembled samples ("dirty" samples with untrusted ends and vectors) to the final output data (the contig cleaned and saved to disk).
With DNA Baser Sequence Assembler, you can also:
- Assemble multiple DNA samples or align to a reference sequence
- Batch assemble or align groups of sequences by name (it will automatically recognize sequence pairs)
- Import and analyze sequences from ABI, SCF, FASTA, SEQ, TXT, GBK
- View and edit sequence traces
- Mark specific regions (like discrepancies, low-quality areas in chromatograms) with visible colors and quickly navigate to these regions
- Convert between different file formats (ABI, SCF, SEQ, FASTA, multi-FASTA, GBK...)
- Automatically integrate metadata in all your contigs
- Automatically detect and remove vectors
