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  • Illumina nextra sequencing

    Hello,

    I'm trying to assemble my illumina sequenced- cyanobacterial genome.. using soapdenovo and velvet, but I'm getting extremely low N50's like less than a 1000. I've never faced such a problem with any of my previous sample genomes.

    Please help!

    bgansw

  • #2
    What have you done to QC your sequences? Are you trimming them? If you map your reads back to the assembly, what insert size to you get? What range of k are you trying?

    Nextera can generate very short insert libraries if things go wrong -- and if you get those, your reads will be badly contaminated with sequencing adapters.

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    • #3
      You're reads were most likely NOT adapter trimmed. This has caused a number of people problems with assembly of Nextera data.

      Do that before assembling and you should get normal looking N50 values.

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