Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Problems with TopHat and Paired End RNASeq

    Hi, I'm very new at RNASeq Analysis and I think that I'm doing something wrong.
    I've tried to align that data: http://trace.ncbi.nlm.nih.gov/Traces...mple=SRS167019.

    First I execute sratoolkit to extract the fastq files with this command:

    fastq-dump --split-3 ./1_SRR097897.sra
    Then I have two files: 1_SRR097897_1.fastq and 1_SRR097897_2.fastq.

    The next step that I've done is to execute TopHat to generate the bam file with the reads aligned. The command was:

    ../tophat2 -N 0 Pombe 1_SRR097897_1.fastq 1_SRR097897_2.fastq
    Then I use the IGB to visualize the results and than shows the + and the - strands are the same



    If I only use one of the _n files to generate the output I have two strands with polarity, but depending on the file to select the polarity is reversed.



    I have also tried running TopHat with different parameters enabling --library-type or a GFF annotation file with identical results.
    I could stay only with the results obtained through _2.fastq file but I wonder to know what I'm doing wrong, for other occasions.

    Thanks for your time!!

  • #2
    I think it makes sense that the different paired ends will be on opposite strands (since you basically read the second end forwards, but on the other strand). At the level of zoom you're at in the included figures, I'm not sure that you could count on seeing the different spacing of the read1s vs the read2s (in my experiments, something like 100-300 bp). It doesn't seem like the best solution, but you could perhaps go through the BAM file and change all of the "SEQ being reverse complemented" bits in the FLAG field to get both ends pointing the same way.

    Comment


    • #3
      Thanks for your answer.
      Finaly I change the reads in one of the FASTQ files to their reverse complementary form and I can align them with polarity but I haven't understood yet why it works :S

      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
      18 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      22 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      16 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      47 views
      0 likes
      Last Post seqadmin  
      Working...
      X