Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sphil
    Senior Member
    • Apr 2010
    • 192

    #1

    Using Tophat with low quality Illumina Reads

    Hello,


    i know that Tophat is one of best choices to get exon-exon structures with short reads but my problem is that the sequencer got problems with their laser while detecting the nt. So all of the reads (completly 82 bp) get an "N" at Postions 54 / 55 of 82. My question ist can TooHat or even BLAT handle this?


    regards

    Philip
  • lifeng.tian
    Member
    • Jul 2009
    • 16

    #2
    Originally posted by sphil View Post
    Hello,
    So all of the reads (completly 82 bp) get an "N" at Postions 54 / 55 of 82. My question ist can TooHat or even BLAT handle this?

    Philip
    Philip,
    I did comparison study between TopHat and BLAT recently on my 75 nt data set. I replaced certain position with N. Both TopHat and BLAT can handle this case well ( two N at position 50,51, TopHat found 164,481 junctions, ie. 1.3% less than original data set).

    Lifeng
    Last edited by lifeng.tian; 05-15-2010, 07:05 AM.

    Comment

    • sphil
      Senior Member
      • Apr 2010
      • 192

      #3
      hey...
      thanks for fast reply i will post my results in case....

      edit:

      i know it should be a new thread but i think its almost a 1 qustion / 1 answer post so:
      can tophat handle long FLX-454 reads? (avg. length of 260bp) or is blat state of the art to get exon-exon structures with long reads?

      greets

      philip
      Last edited by sphil; 05-15-2010, 04:40 AM.

      Comment

      • lifeng.tian
        Member
        • Jul 2009
        • 16

        #4
        Originally posted by sphil View Post
        hey...

        can tophat handle long FLX-454 reads? (avg. length of 260bp) or is blat state of the art to get exon-exon structures with long reads?

        philip

        with my illumina data (130 nt, paired), BLAT works better than TopHat, it
        found 10% more known Refseq splice junctions.

        It'll be interesting to compare both with your data. My bet is BLAT will win

        Comment

        • sphil
          Senior Member
          • Apr 2010
          • 192

          #5
          hey, ok i will brief you if anything unpredictable will happen!

          Comment

          • ParthavJailwala
            Member
            • Oct 2009
            • 27

            #6
            Originally posted by sphil View Post
            Hello,


            i know that Tophat is one of best choices to get exon-exon structures with short reads but my problem is that the sequencer got problems with their laser while detecting the nt. So all of the reads (completly 82 bp) get an "N" at Postions 54 / 55 of 82. My question ist can TooHat or even BLAT handle this?


            regards

            Philip
            Hi Philip,
            Tophat internally uses Bowtie which has a combination of parameters that you can adjust to allow it to map in the presence of 'n' mismatches ( I am assuming a 'N' at any position is treated as a mismatch by the algorithm). Some of these parameters are:

            --initial-read-mismatches Reads are initially mapped, allowing up to this many mismatches in each read alignment. The default is 2.

            --segment-mismatches Read segments are mapped independently, allowing up to this many mismatches in each segment alignment. The default is 2.

            -m/--splice-mismatches <int> The maximum number of mismatches that may appear in the "anchor" region of a spliced alignment. The default is 0.

            Hope that helps,

            Thanks

            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
            52 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-22-2026, 10:48 AM
            0 responses
            39 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-15-2026, 10:52 AM
            0 responses
            46 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-14-2026, 05:39 AM
            0 responses
            46 views
            0 reactions
            Last Post SEQadmin2  
            Working...