Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • DMNO
    Junior Member
    • Sep 2017
    • 3

    "Stranded" data may actually be unstranded?

    Hello!

    I have some paired-end RNA-seq data that I was told were "stranded", but nothing about whether it's RF or FR.

    I aligned some randomly sampled pairs of reads to the reference genome of the organism. I see that 50% of the read 1s map to the "+" strand, the other 50% to the "-" strand. Same as the read 2s.

    Does this mean that the data is actually unstranded?

    P.S. I can't get QoRTs to work on my data, so I can't use it to tell me whether the data is stranded or not.

    Thank you!
  • Michael.Ante
    Senior Member
    • Oct 2011
    • 127

    #2
    Hi DMNO,

    did you take the transcripts' strand-orientation into account? Try using RSeQC's infer-experiment tool. It gives you a good way to assess if your library was stranded and in which orientation.

    Cheers,

    Michael

    Comment

    • DMNO
      Junior Member
      • Sep 2017
      • 3

      #3
      Thank you very much, Michael!

      The output of infer_experiment.py is:


      Fraction of reads failed to determine: 0.0098
      Fraction of reads explained by "1++,1--,2+-,2-+": 0.0089
      Fraction of reads explained by "1+-,1-+,2++,2--": 0.9813


      From what I understand, this means that the library is RF?

      Comment

      Latest Articles

      Collapse

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Today, 10:09 AM
      0 responses
      9 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, Yesterday, 08:59 AM
      0 responses
      15 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-02-2026, 12:03 PM
      0 responses
      24 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-02-2026, 11:40 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Working...