Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Illumina MiSeq read orientiation

    Hi all,
    I've got RNA-seq paired-end Illumina MiSeq data. I'm stuck with which read now represents the forward strand, and which one the reverse complement strand. When mapping, which read (R1/R2) should map (equals part of) to the 5' -> 3' reference sequence? And which one should map to its reverse complement?

    [Header]
    IEMFileVersion,4
    Experiment Name,sampleA
    Date,12/10/2013
    Workflow,GenerateFASTQ
    Application,RNA-Seq
    Assay,TruSeq LT
    Description,
    Chemistry,Default
    Last edited by Puhekupla; 02-26-2014, 04:03 AM.

  • #2
    Unless the library-prep was done using a strand-specific protocol,
    the reads will map to both strands.

    In the Illumina system, the two reads of a pair, R1 and R2, will map to different strands.

    Comment


    • #3
      Yes, but which one of the pair maps to the forward reference sequence, and which one to the reverse complement? (Or should).
      Last edited by Puhekupla; 02-26-2014, 04:11 AM.

      Comment


      • #4
        Originally posted by Puhekupla View Post
        Yes, but which one of the pair maps to the forward reference sequence, and which one to the reverse complement? (Or should).
        For each pair, one read will be mapped to one strand of the reference genome, the other will be mapped to the other strand of the reference genome (i.e. reverse complementary to the first strand). So you question can be translated into "will the first read of a pair definitely be mapped to the positive strand of the reference genome or definitely be mapped to the negative strand of the reference genome?". Of course, the answer is NO.

        Comment


        • #5
          In my case:

          R2 is the forward
          R1 is the reverse

          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
          17 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
          46 views
          0 likes
          Last Post seqadmin  
          Working...
          X