DNA sequence assembly, contig editign, molecular biology software
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trace alignment

DNA Baser Sequence Assembler

Tired of manual DNA sequence analysis/assembly?

 

 

DNA chromatogram alignment

 

Why is DNA Baser better than other tools?

How it triples your productivity?

Thousands of contigs in minutes?

Only two minutes to learn to use it

Did you say "affordable price"?

Who is using DNA Baser Sequence Assembler?

 

DNA sequence assembly software. Automatic ambituity correction, automatic end trimming, automatic vector removal

 

Full working trial - Instant download

Download DNA sequence alignment software

 

DNA Baser Sequence Assembler is revolutionary bioinformatics software for manual and automatic DNA sequence assembly , DNA sequence analysis, contig editing, file format conversion and mutation detection.

Its unbeatable price and the truly user-friendly interface makes DNA Baser the modern choice for DNA sequence assembly.

 

 

DNA Baser Sequence Assembler is the only tool that fully automates the assembly process:

  • Automatically detect and trim low quality regions of your samples
  • Automatically trim vector/primer sequences
  • Automatically correct the ambiguities in your contig
  • Automatically save the project and the contig to disk

With DNA Baser you need ONLY 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 or align multiple DNA samples to a reference sequence
  • Batch assemble or align groups of sequences by name (it will automatically recognize sequence pairs)
  • Preview FASTA sequences and chromatograms as you navigate through your folders
  • View, analyze and edit ABI, SCF, FASTA, SEQ, TXT, GBK sequences
  • Mark specific chromatogram regions (like discrepancies, low-quality areas) with colors & quickly navigate to these regions
  • Convert or batch-convert between different file formats (ABI, SCF, SEQ, FASTA, multi-FASTA, GBK...)
  • Detect double peak mutations
  • Detect mutations between two (or more) chromatograms
  • Use the embedded base caller to re-call undetermined (N) bases
  • Reassess the base quality (QV)
  • Easily overview your project using the synchronized chromatogram/assembly grid/contig map

DNA fragment alignment, sequence analysis and editing, assemble to reference, sequence alignment/sequence analysis

 


 

DNA Baser Sequence Assembler in action

 

With DNA Baser literally need only 5 seconds to clean low quality regions in your sequences, to assemble the sequences into a contig, remove vectors/primes, automatically fix ambiguities and mismatches and to save the contig to disk. The movie below demonstrates how quickly you can have your contig done:

 

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DNA sequence alignment software
   
Heracle BioSoft S.R.L.