Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dschika
    Member
    • Mar 2010
    • 56

    #1

    Find SNP in 454HCDiffs.txt

    Hey there,

    I mapped my reads against a reference consisting of the isotigs of the de novo assembly of the same reads. I'm wondering now if the follwoing approach is really sufficient to detect SNPs in the 454HCDiff.txt:
    - get the summary line of each diff: grep '>' 454HCDiffs.txt
    - check if the start and end position are identical (SNPs need to be at the same position in the reference)
    - check if neither the ref nucleotide nor the var nucleotide is only a gap

    - check if the var nucleotide length is 1

    Regards,
    Thomas
    Last edited by dschika; 01-18-2011, 03:46 AM.
  • nickloman
    Senior Member
    • Jul 2009
    • 355

    #2
    Yes, that approach will give you a list of putative SNP/SNVs.

    But you will want to do further filtering (e.g. on read depth, quality) to get a more trusted set of SNPs.

    Comment

    • dschika
      Member
      • Mar 2010
      • 56

      #3
      Thanks for your quick reply!

      I thought it would be sufficient to take the 454HCDiffs.txt file, because of the High Confidence. That means that (please see the manual for full details):
      - there must be at least 3 non-duplicate reads with the difference
      - there must be forward and reverse reads with the difference, unless there are at least 5 reads with quality score over 20

      Do you think that those filtering options are still too smooth? Can you perhaps suggest some other values?

      Btw: I added another step in my first post.

      Comment

      • nickloman
        Senior Member
        • Jul 2009
        • 355

        #4
        It will depend on a number of factors. For example if you have greater coverage then you might want to set the read depth cut-off higher. It will depend also on the quality of your reference genome - that might have errors in it. You need to take a view depending on what you are trying to do.

        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, 10-22-2026, 11:13 AM
        0 responses
        42 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        33 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        44 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        45 views
        0 reactions
        Last Post SEQadmin2  
        Working...