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De novo Genome Assembly

DNASTAR's de novo sequence assembly software allows users to quickly and easily perform de novo assemblies using either long read platforms such as the Roche 454 Life Sciences system or shorter read data generated from Illumina, SOLiD or Helicos instruments. Features of the software enable users to:

  • Assemble either single-end or paired-end data
  • View contig scaffolds along with the paired sequences that tie the contigs together
  • Annotate gaps in the scaffold consensus

    • See a video of this workflow:

    Additional Details

    For more information on how DNASTAR can help with your de novo assemblies and other next generation sequence assembly and analysis, see our SeqMan NGen and Lasergene Core Suite pages.