Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Pejman
    Member
    • Jul 2010
    • 23

    #1

    Tuning TopHat parameters for SOLiD reads

    Hi folks

    The new TopHat 1.1.1, nicely handles SOLiD reads, and the results can be piped easily to Cufflinks to make up a RNAseq pipeline. However, the manual page says:

    In TopHat 1.1.0, we began supporting Applied Biosystems' Colorspace format. The software is optimized for reads 75bp or longer.
    and there are no further guidelines how to tune the parameters if you have shorted reads, as in my case 30bp single-end. Does anybody have any clue on this? Of course this is tunable through editing the TopHat scripts but, the question is how to set the parameters not to screw the whole thing up

    I did a comparison, using TopHat+GTF file and defaults parameters, I get about 5 times less aligned tags than what I get from Bowtie with some sensible parameters.
    Last edited by Pejman; 10-15-2010, 08:59 AM.
  • mrawlins
    Member
    • Apr 2010
    • 63

    #2
    Based on my limited understanding of how TopHat works, I would be very hesitant to use reads as short as 30bp. It seems to me you would have a pretty good chance of either the front or the back of the read (before or after the splice) mapping to random sections of the genome that way. For a small genome (like something microbial) that may not be too much of a problem. For anything comparable in size to human I would be extremely hesitant to trust any junction mapping without at least 40bp, and not very confident without 50+, as that would allow for a few mismatches before random matches became a serious problem.

    Comment

    • Pejman
      Member
      • Jul 2010
      • 23

      #3
      well, I'm working with human data, so ... but I'm not looking for new junctions, so I'm running it using predefined junctions from RefSeq and --no-new-junctions option, both for Tophat and Cufflinks. Now I've ran Bowtie -> cufflinks which is not recommended by the authors, and TopHat -. Cufflinks, which is recommended, but heavily fails on the alignment step. I'm gonna do some comparison, I'll keep you updated in case of any conclusive observations! Suggestions are welcome!

      Comment

      • waterboy
        Member
        • Oct 2010
        • 14

        #4
        Hello Pejmen,

        I am Shilp Purohit, and I am currently working with ABI SOLiD 3 plus sequencer. I am trying to install TopHat 1.1.2 (BETA) on my local machine. The "Getting started" manual suggests that I need to run following commands:

        ./configure
        make
        make install

        However, the unzipped tar package doesn't have these files to execute, i.e. configure, make file and install file.

        On the other hand, I unzipped tar package of TopHat version 1.1.0 and it worked absolutely fine and installed correctly just because the package consisted of these three files. But this version doesn't support the colorspace format of SOLiD.

        Can you please suggest me as to how to install version 1.1.2? Any suggestions will be highly appreciated.

        I am looking forward to having a reply soon.

        Thanking you.

        Comment

        • Pejman
          Member
          • Jul 2010
          • 23

          #5
          Hi
          The last version I've used was 1.1.1 and that supports CS data. I recommend you to just use the precompiled versions, if you have problem with compiling. I checked the source files for 1.1.2, the configure file is there!

          Comment

          • JohnK
            Senior Member
            • Feb 2010
            • 106

            #6
            How risky do you consider 50 bp reads?

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
              by SEQadmin2



              CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

              Despite this, “CRISPR helped turn genome editing from a specialized technique into
              ...
              Yesterday, 11:01 AM
            • 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

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, Yesterday, 02:55 AM
            0 responses
            12 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            12 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-23-2026, 11:41 AM
            0 responses
            13 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-20-2026, 11:10 AM
            0 responses
            24 views
            0 reactions
            Last Post SEQadmin2  
            Working...