Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • jameslz
    Member
    • Nov 2009
    • 20

    tophat 1.3.0 sam output quality string problem

    When I mapped the RNA-seq data to reference genome using tophat 1.3.0 ,I met a problem in the sam output. but the version 1.2.0 did not have such situation.
    Here is the result:
    1. The tophat 1.3.0 result:
    HWI-ST_0101:7:8:14864:67306#0 99 scaffold_8 3915632 255 95M = 3915887 420 GGACCGGTAGAAATTTTCCAATGAGAGATCATGTGAAGATTGAAAAGAAGAGTCCATGACAAATTTACATTGGCTGCTGCAATAGCTGAGGAGCG HHHHHHHFHHHHBHHHHHHFHHHHHFHFFHFGGEGFEGEGGGCFECHHHHHHEHHHFHEEBBEFG@AFFFDFFFFF54;.9;4*.:>>8@B#### NM:i:1 NH:i:1
    HWI-ST_0101:7:8:14864:67306#0 147 scaffold_8 3915887 255 68M70N27M = 3915632 420 TTTCCAAGTCATCCTCGTTGCCAATCGGTGCTTGACCGTCTTGCTGGGCCTCATGGATGCGACGATGTTGTGCCAGGTTGTCTGATCGAGAAAAG * NM:i:0 XS:A:- NH:i:1
    2. The tophat 1.2.0 result:
    HWI-ST_0101:7:8:14864:67306#0 99 scaffold_8 3915632 255 95M = 3915887 0 GGACCGGTAGAAATTTTCCAATGAGAGATCATGTGAAGATTGAAAAGAAGAGTCCATGACAAATTTACATTGGCTGCTGCAATAGCTGAGGAGCG HHHHHHHFHHHHBHHHHHHFHHHHHFHFFHFGGEGFEGEGGGCFECHHHHHHEHHHFHEEBBEFG@AFFFDFFFFF54;.9;4*.:>>8@B#### NM:i:1 NH:i:1
    HWI-ST_0101:7:8:14864:67306#0 147 scaffold_8 3915887 255 68M70N27M = 3915632 0 TTTCCAAGTCATCCTCGTTGCCAATCGGTGCTTGACCGTCTTGCTGGGCCTCATGGATGCGACGATGTTGTGCCAGGTTGTCTGATCGAGAAAAG *?EFEGGGEGD>GGEGGDFHHHEHEHHHHFHHHHFGGFFHDFHHGGHHHHHHHHHHHHGHHFHHHHHHFHHHHHHHHHHHHHHHHHHHHHHHHHF NM:i:0 XS:A:- NH:i:1

    whe I use htseq-count , It gives error report.
    python -m HTSeq.scripts.count accepted_hits.unique.sam ../../../pde.release.v3.gff
    39609 GFF lines processed.
    Error occured in line 876 of file accepted_hits.unique.sam.
    Error: ("'seq' and 'qualstr' do not have the same length.", 'line 876 of file accepted_hits.unique.sam')
    [Exception type: ValueError, raised in _HTSeq.pyx:765]

    is it a bug?
  • jameslz
    Member
    • Nov 2009
    • 20

    #2
    A more question:
    Tophat can't handle reads with different size of length ?

    Comment

    • maubp
      Peter (Biopython etc)
      • Jul 2009
      • 1544

      #3
      The SAM files look OK to me. Notice that in tophat 1.3.0 one of the quality strings is a single * which means data not available, while with tophat 1.2.0 you do get a full quality string which happens to start with a * character (which is valid).

      So, that could be a bug in tophat 1.3.0 (using * for missing qualities when it probably does know them), and a separate bug in htseq-count failing to accept * for missing qualities.

      What version of htseq-count are you using? I had a quick look at HTSeq-0.5.1p2.tar.gz file src/HTSeq/_HTSeq.pyx and there is no obvious sign that they cope with this situation (but I didn't fully explore their code).

      P.S. I've emailed Simon Anders about this possible HTSeq issue.
      Last edited by maubp; 06-16-2011, 02:05 AM.

      Comment

      • jameslz
        Member
        • Nov 2009
        • 20

        #4
        Originally posted by maubp View Post
        The SAM files look OK to me. Notice that in tophat 1.3.0 one of the quality strings is a single * which means data not available, while with tophat 1.2.0 you do get a full quality string which happens to start with a * character (which is valid).

        So, that could be a bug in tophat 1.3.0 (using * for missing qualities when it probably does know them), and a separate bug in htseq-count failing to accept * for missing qualities.

        What version of htseq-count are you using? I had a quick look at HTSeq-0.5.1p2.tar.gz file src/HTSeq/_HTSeq.pyx and there is no obvious sign that they cope with this situation (but I didn't fully explore their code).

        P.S. I've emailed Simon Anders about this possible HTSeq issue.
        Thanks for your answer.
        I use the latest version HTSeq-0.5.1p2.

        Comment

        • jameslz
          Member
          • Nov 2009
          • 20

          #5
          Originally posted by jameslz View Post
          A more question:
          Tophat can't handle reads with different size of length ?
          if I trim the low quality base from the 3' end , I can map 80% paired reads to the reference, if not, just 70% paired reads can be mapped to genome.

          can anyone help me?

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
            by SEQadmin2


            Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


            The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
            ...
            06-02-2026, 10:05 AM
          • SEQadmin2
            Single-Cell Sequencing at an Inflection Point: Early Impacts of New Platforms and Emerging Trends
            by SEQadmin2


            With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.


            Introduction

            Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...
            05-22-2026, 06:42 AM
          • SEQadmin2
            Environmental Genomics in the Age of NGS: From Microbes to Conservation Strategies
            by SEQadmin2

            Studying ecosystems means dealing with complex, multi-species communities that are hard to observe at scale. This complexity, however, hides many important questions to be answered, from how biogeochemical cycles work and how climate change can affect species distribution to how conservation strategies can work best.


            Genomics, particularly since the expansion of NGS, has transformed ecosystem ecology. By sequencing environmental DNA, we can now assess biodiversity without direct...
            05-06-2026, 09:04 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 06-02-2026, 12:03 PM
          0 responses
          19 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-02-2026, 11:40 AM
          0 responses
          14 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 05-28-2026, 11:40 AM
          0 responses
          29 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 05-26-2026, 10:12 AM
          0 responses
          31 views
          0 reactions
          Last Post SEQadmin2  
          Working...