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  • jmtepp
    Junior Member
    • Jul 2010
    • 1

    #1

    Analysis of Directional mRNA-seq data / Illumina

    We are developing a library preparation for directional mRNA-seq. All sequences will read 5' -> 3' direction. Our protocol isolates mRNA, fragments the messages and then these are re-purified with oligodT - resulting in a library of short 3' fragments for sequencing. This eliminates the need to adjust for transcript length when doing quantitative expression analysis. We're using bowtie to align the raw reads to a (cDNA) reference transcriptome (minus introns and intergenic regions). BUT - approximately 12% of the loci in this organism (Arabidopsis) have overlapping 3' tails (Watson/Crick strands) leading to ambiguities when using BowTie ( which looks for alignments on both strands). Basically we're looking for a short read alignment algorithm that would take our directional data and align it ONLY with transcripts in the 5' -> 3' direction. Illumina is developing a directional mRNA-seq library prep method similar to the one we are using (without the purification of the 3' ends). I wonder if anyone has experience analyzing directional mRNA-seq data?
  • HESmith
    Senior Member
    • Oct 2009
    • 512

    #2
    Since your libraries are directional, you can use that information to resolve the ambiguity of overlapping 3' ends. The tag will be in the same 5'->3' direction as one of the two genes (conventionally indicated as +).

    Harold

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    • Simon Anders
      Senior Member
      • Feb 2010
      • 995

      #3
      Originally posted by jmtepp View Post
      Basically we're looking for a short read alignment algorithm that would take our directional data and align it ONLY with transcripts in the 5' -> 3' direction.
      As you are already using Bowtie, have a look at its manual again, especially at the description of the option '--norc'. It causes Bowtie to do precisely this.
      Last edited by Simon Anders; 12-04-2010, 05:10 AM. Reason: sp

      Comment

      • qqtwee
        Member
        • Feb 2011
        • 16

        #4
        strand specific RNA-seq mapping

        Does anyone know how do mapping for strand specific RNA-seq data? which tools can work well? what the parameter of tools for strand specific infomation of RNA-seq data?
        Looking forward to your answer.
        Thank you very much! Best wishes!

        Comment

        • jujubix
          Member
          • May 2011
          • 14

          #5
          Originally posted by qqtwee View Post
          Does anyone know how do mapping for strand specific RNA-seq data? which tools can work well? what the parameter of tools for strand specific infomation of RNA-seq data?
          Looking forward to your answer.
          Thank you very much! Best wishes!
          Maybe TopHat with the '--library-type' option which will treat the reads in a strand specific manner as described in the manual?

          Comment

          • qqtwee
            Member
            • Feb 2011
            • 16

            #6
            Originally posted by jujubix View Post
            Maybe TopHat with the '--library-type' option which will treat the reads in a strand specific manner as described in the manual?
            Thank you for your reply! Do you know BWA has option that can treat reads in a strand specific ?

            Comment

            • jujubix
              Member
              • May 2011
              • 14

              #7
              Originally posted by qqtwee View Post
              Thank you for your reply! Do you know BWA has option that can treat reads in a strand specific ?
              No, I do not know. Although the manual probably says no?

              Comment

              • stanikay
                Junior Member
                • Oct 2013
                • 4

                #8
                Mappind strand specific RNAseq bacteria pair-end reads

                Just following up on this thread, which mapper will be most ideal for mapping strand specific RNAseq bacteria pair-end reads,

                I know tophat has the library type option but its mostly ideal for eukaryotic genomes.

                Any thoughts will be appreciated.

                Thanx

                Comment

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