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  • Whole genome assembly

    It might be a naive question:

    After aligning agaist a reference genome, we can get sorted consensus sequences for each chromosome. My question is how to integrate the unmapped reads to generarte a distinct whole genome sequence?

    Is De novo assembly of all the reads (mapped and unmapped, paired-end and single-end) doing this job?

    Thanks

  • #2
    Originally posted by bair View Post
    It might be a naive question:

    After aligning agaist a reference genome, we can get sorted consensus sequences for each chromosome. My question is how to integrate the unmapped reads to generarte a distinct whole genome sequence?

    Is De novo assembly of all the reads (mapped and unmapped, paired-end and single-end) doing this job?

    Thanks
    I am afraid some of the unmapped reads are not from the genome, such as adaptors, or with too much sequencing errors.
    Xi Wang

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    • #3
      Yes, I agree. And some of the unmapped reads may be DNA contamination from different species.

      Ling

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      • #4
        Still, for whole genome assembly, you can try the tool - SOAPdenovo.

        Xi Wang

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        • #5
          Thank you guys.

          For whole genome, soapdenovo needs >150G RAM, that's expensive. worthy to try.

          Comment

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