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SNP Discovery in "Deep" Assemblies

DNASTAR provide tools to simplify your SNP discovery and analysis with data generated by Next Generation sequencing platforms offered by Roche 454 Life Sciences, Illumina, ABI SOLiD, and Helicos as well as Sanger instruments. The ability of Next-Gen instruments to perform "deep" assemblies can present users with unique SNP analysis problems. DNASTAR's software provides users with the tools required to overcome these problems. Features of the software enable users to:

  • Assemble accurately to depths of 200,000 reads or more at individual base locations
  • Selectively filter SNPs for customized searches
  • Examine sequences and related information surrounding specific SNPs

    • See a video of this workflow:

    Additional Details

    For more information on how DNASTAR can help with your SNP assembly and analysis projects and other next generation sequence applications see SeqMan NGen and Lasergene.