Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Multi-read problem with bowtie and cufflinks

    Hi,

    I am trying to use the sorted BAM files (samtools) from bowtie alignments with cuffdiff.

    Although I allow bowtie to report multiple matching reads cuffdiff reports:
    Multi-Reads: 0

    The same cuffdiff parameters used for a TopHat alignment of the same data does show Multi-Reads!

    Any ideas what could be the problem?

    Thanks a lot!

  • #2
    Did you find the solution.

    I had the same problem as you posted last year on this forum.
    I wonder if you found the solution how to deal with the multi-read in bam file generated by Bowtie.
    Thanks.

    Comment


    • #3
      There seem to be some people interested as this post has 434 views but no replies.

      So I investigated the matter and found the following:
      Cuffdiff needs a certain nomenclature for multi-reads in the BAM file. This nomenclature is non-standard (at least for bowtie alone) but done by TopHat automatically. What TopHat basically does is to connect the multireads and make the analysis for cufflinks easier.

      At the moment I use TopHat with a GTF file for my reference transcripts and use this output for cufflinks. This is quite quick and does the job.

      I wished the tuxedo-suite developers cared more for their users and give this information somewhere ...

      hope this helps,

      Comment


      • #4
        Thanks~

        Thank you very much for the information.
        Recently launched Bowtie2 generates much sensitive alignment compared to the previous Bowtie. So, I tried to avoid using Tophat because it still uses old Bowtie for its process.

        Comment

        Latest Articles

        Collapse

        • seqadmin
          Current Approaches to Protein Sequencing
          by seqadmin


          Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
          04-04-2024, 04:25 PM
        • seqadmin
          Strategies for Sequencing Challenging Samples
          by seqadmin


          Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
          03-22-2024, 06:39 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, 04-11-2024, 12:08 PM
        0 responses
        25 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        28 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 09:21 AM
        0 responses
        24 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-04-2024, 09:00 AM
        0 responses
        52 views
        0 likes
        Last Post seqadmin  
        Working...
        X