Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • bioenvisage
    Member
    • Oct 2009
    • 40

    Perl script

    Can any one help me with a perl script for removing the repeats in the reads , for eg i will paste the format of the seq below

    HWI-EAS373:2:100:1792:1509#0/1 AAAAAAAAAAAAAAAAAACAACAAAAAAACAAAACAAAAACAAAACCAACACC ]_a`_Z_IT`b_\[_Ya\[\[]S\[RHUR^a^YY_V]aa^[TaW\Y\W_`^][aYR_BBBBBBBBBBBBBBBBBBB NF
    HWI-EAS373:2:100:1792:1509#0/2 ACACACACATGGTCCACCATATTTTTTTACTTGGTTGTA aRaPZ__\__]VG[]RMGX\_Z_aa_P_NQ[_\VTFZTOa`R_[Q]ZZZXaBBBBBBBBBBBBBBBBBBBBBBBBB NF
    HWI-EAS373:2:100:1792:1691#0/1 ACACACACAGTGTAGCTGGGGAGCAGGGATCCATTGATC abaa^]Waa]b_`Vb_b`aa[^`aa_aaXD^H]`]QWYa`ZaZaH]`TMS]`^BBBBBBBBBBBBBBBBBBBBBBB NF
    HWI-EAS373:2:100:1792:1691#0/2 GGCTTTTTTGGTATCCTTTTCTCATGTTAGATGATGGGAGCATTTTTCTTCAGTgggatggatggtctggtagggc a^aY`_aaVa`UUabWaWa_bab_`a`b`aaOb``YN[a]GR`a`a`ba]_[J[XYBBBBBBBBBBBBBBBBBBBB NF
    HWI-EAS373:2:100:1792:198#0/1 CGGCATTCCTTTTATTATAGCCCCTCTAGCTAGTTACAGTAGATAGGAACGtgcatgaatctntaaatggntgnan aZ]`]ab``aaab`a`]`YT`a^`aa`UZ\^X_Y]^Z^aYY[TYV[\XVLYBBBBBBBBBBBBBBBBBBBBBBBBB NF
    HWI-EAS373:2:100:1792:198#0/2 agCTGATCTAGCGTCGTCTGCAACAACAACCGCGGGGGCGTCatcaacggcaagtgcggctcagcctcgggtgttg HOT_TTGYZGV_]GUQ_XNGSQZ\QIYTXT\_RKQGGL]O\ZBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB NF
    HWI-EAS373:2:100:1793:876#0/1 CCNCTGCCTCTACCTCCACGCCCTCGGCCTCTGCCACGCCCGCGGCCTGTATCTccagtgctctactcgcacanan `WDV^`a``a`aa^a`_aa[a]aY[`a\][a`\^``\`\]\^^S]Z[ZXW]ZP\SQBBBBBBBBBBBBBBBBBBBB NF
    Last edited by bioenvisage; 01-28-2010, 06:43 AM.
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    I'm having trouble making out what the data should look like - try wrapping the example with code tags,
    [ code ] sequence data [ /code ]

    Comment

    • krobison
      Senior Member
      • Nov 2007
      • 734

      #3
      By repeats in the reads do you mean
      (a) Within a read, the repetition of a single nucleotide or simple sequence
      (b) For sets of reads which are identical (presumed PCR duplicates), report only one
      (c) Something else

      SAMTools will do (b)

      Comment

      • Dave S.
        Junior Member
        • Jan 2010
        • 5

        #4
        If you just want to remove homopolymers of DNA of some arbitrary length, use something like:
        Code:
        $min = 4;
        
        while (<>)
        {
        s/(G){$min,}|(A){$min,}|(T){$min,}|(C){$min,}/$1$2$3$4/g;
        print;
        }
        You are probably better off determining where and when they occur before wiping them out, e.g. see http://www.bioperl.org/wiki/Finding_...hes_in_contigs

        If your sequencing method is generating spurious homopolymers you will need a much more sophisticated approach to determining which ones are real.

        Comment

        • bioenvisage
          Member
          • Oct 2009
          • 40

          #5
          hi krobison ...iam telling about with in the read the repetation of single nucleotide and also simple repeats.

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
            by SEQadmin2


            Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

            The systematic characterization of the human proteome has
            ...
            07-20-2026, 11:48 AM
          • SEQadmin2
            Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
            by SEQadmin2



            Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
            ...
            07-09-2026, 11:10 AM
          • SEQadmin2
            Cancer Drug Resistance: The Lingering Barrier to Rising Survival
            by SEQadmin2



            Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

            There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
            07-08-2026, 05:17 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 07-24-2026, 12:17 PM
          0 responses
          30 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-23-2026, 11:41 AM
          0 responses
          23 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-20-2026, 11:10 AM
          0 responses
          213 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-13-2026, 10:26 AM
          0 responses
          79 views
          0 reactions
          Last Post SEQadmin2  
          Working...