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  • super0925
    Senior Member
    • Feb 2014
    • 206

    #1

    How to generate a transcript sequence derived obtained in the RNAseq?

    In RNA-Seq, While we have our list of DE genes, selecting a specific transcript/isoform for gene synthesis is not straight forward. How to generate a transcript sequence derived from a contig of the transcript sequences obtained in the RNAseq experiments? Cheers
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Are you asking if an overall consensus sequence can be generated for a gene from a set of mapped reads?
    Last edited by GenoMax; 03-10-2015, 09:11 AM.

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    • super0925
      Senior Member
      • Feb 2014
      • 206

      #3
      Originally posted by GenoMax View Post
      Are you asking if an overall consensus sequence can be generated for a gene from a set of mapped reads?
      Yep. consensus sequence for each gene could be interesting
      Thanks.
      How to do that?
      Last edited by super0925; 05-14-2015, 08:35 AM.

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      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        If you have a linear contig then isn't that the consensus sequence for that transcript or are you referring to a region in the alignment file (where multiple reads are piled up) that you want to derive a consensus sequence from?

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        • super0925
          Senior Member
          • Feb 2014
          • 206

          #5
          Originally posted by GenoMax View Post
          If you have a linear contig then isn't that the consensus sequence for that transcript or are you referring to a region in the alignment file (where multiple reads are piled up) that you want to derive a consensus sequence from?
          For a particular gene, what is the splice variance ? from Alignment file e.g. bam or sam.

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          • super0925
            Senior Member
            • Feb 2014
            • 206

            #6
            Originally posted by GenoMax View Post
            If you have a linear contig then isn't that the consensus sequence for that transcript or are you referring to a region in the alignment file (where multiple reads are piled up) that you want to derive a consensus sequence from?

            ‘If you have a linear contig then isn't that the consensus sequence for that transcript’
            Yes. And how to get the contigs for each?
            I want output a sequence as a result of generating a contig from the mapped sequence data. Thank you!
            Last edited by super0925; 05-29-2015, 02:44 AM.

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