Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • fznajar
    Member
    • Jan 2012
    • 35

    #1

    Deciding how many reads map to a plasmid or to a genome

    Hi all,
    I have illumina genome reads for an E. coli a collaborator is studying. The prep used had a plasmid as well. I have two questions:

    1) For the reads that match both (e.g. lacI gene), how can I tell which came from the plasmid and which came from the genome?
    2) Should I normalize by dividing on the total reads per library or only the mapped reads in a library?

    Thanks in advance...
    Last edited by fznajar; 01-09-2019, 01:44 PM.
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    #1 = Unless there is/are SNP's which are captured by that particular read you would not be able to tell where the read came from. I assume the sequence of the gene is otherwise identical?

    Comment

    • fznajar
      Member
      • Jan 2012
      • 35

      #3
      You are correct GenoMax. They are identical. Appreciate it.
      Best

      Comment

      • seb567
        Senior Member
        • Jul 2008
        • 260

        #4
        If you'are using "bwa sampe" for aligning, the documentation says:

        Generate alignments in the SAM format given paired-end reads. Repetitive read pairs will be placed randomly.
        I don't know if it is the case with "bwa mem" or with "bwa aln".

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
          by SEQadmin2



          Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

          Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
          ...
          10-14-2026, 09:55 AM
        • SEQadmin2
          New Genomics Technologies Take Aim at Long-Standing Limits
          by SEQadmin2


          Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

          We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
          ...
          09-28-2026, 10:25 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 11:13 AM
        0 responses
        19 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        18 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        36 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        42 views
        0 reactions
        Last Post SEQadmin2  
        Working...