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  1. Expand
    titleHow many contigs were generated in each case?

    2 for the plasmid and 16 for the full

    Code Block
    languagebash
    titleWhere does the answer come from?
    collapsetrue
    grep -c "^>" unmapped*/contigs.fasta
  2. Expand
    titleAre any of the contigs the same?

    Yes, both contigs detected in the plasmid mode were also detected in the full mode

    Code Block
    languagebash
    titleWhere does the answer come from?
    collapsetrue
    grep "^>" unmapped*/contigs.fasta
    # lists identical lengths and coverages for 2 plasmid contig
  3. Expand
    titleWhat sizes are the contigs?

    5441

    3170

    14 others less than 500bp

    Code Block
    languagebash
    titleWhere does the answer come from?
    collapsetrue
    grep "^>" unmapped*/contigs.fasta
    # same command as above, just focusing on the length value
  4. Expand
    titlewhich is most likely to be our plasmid?

    The contig that is 3170.

    Code Block
    languagebash
    titleWhere does the answer come from?
    collapsetrue
    # From above, I stated this was a high copy plasmid, it has a coverage value of 12,698 compared to 98 for the larger contig
  5. Expand
    titleIs that actually our plasmid?

    Yes! The actual plasmid reference locus line stats:

    LOCUS       GFP_Plasmid_Sequ        3115 bp    DNA     circular UNA 18-NOV-2013

    Expand
    titleWhy might the sizes not agree?

    My thought is that this was raw fastq files that were fed into the assembly, not trimmed files. Leads me to hypothesize that the difference in size is related to the presence of adapter sequence.


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