Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Rhodotus
    Junior Member
    • Jan 2013
    • 1

    #1

    Filter paired end based on GC content

    Our genomic libraries (Arabidopsis) are contaminated with an endophytic bacteria and we would like to filter out this contaminant.

    Is there any tool out there, which can filter paired reads based on GC content ?

    I have not found many filtering tools respecting the paired end order. Trimmomatic was a very good one for other sorts of filters but lacks GC content option. Prinseq can filter after GC content but not in paired end ones. An alternative could be a tool selecting paired end reads from two unpaired files.

    Cheers.
  • maasha
    Senior Member
    • Apr 2009
    • 153

    #2
    You can use Biopieces (www.biopieces.org) for this:

    Code:
    read_fastq -i in.fq | analyze_gc | grab -e 'GC% >= 65' | order_pairs | write_fastq -o out.fq -x
    This solution works, but may feel slow since Biopieces don't assume that the order of entries are pre-sorted. A Perl hack will be faster (depending on how fast you are at writing and proofing the code).

    Comment

    • JackieBadger
      Senior Member
      • Mar 2009
      • 385

      #3
      PRINSEQ

      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
        ...
        Today, 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, Today, 05:39 AM
      0 responses
      10 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, Yesterday, 09:56 AM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-09-2026, 11:14 AM
      0 responses
      26 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 09-29-2026, 09:51 AM
      0 responses
      77 views
      0 reactions
      Last Post SEQadmin2  
      Working...