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  • lilichen
    Junior Member
    • Dec 2014
    • 6

    #1

    good QC mRNA seq samples with super low alignement

    Hi, Everybody:

    We just completed mRNA seq for some human cells bulk samples.
    The QC for those seq data is good. But when we run the alignment for those samples, super low alignment rate come out ( ~50%). We built those lib samples by the pico-input stranded mRNA prep kit from Clontech.

    Is there any body have experience for this wired low alignment rate issue?
    Is there something wrong about the quality of original samples? or lib prep process? or seq running process?

    Any advice would be appreciated.
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Take a sample of the reads that did not align and check using NCBI blast. Did you use an aligner that is splice aware and use appropriate settings for it?

    Comment

    • lilichen
      Junior Member
      • Dec 2014
      • 6

      #3
      Originally posted by GenoMax View Post
      Take a sample of the reads that did not align and check using NCBI blast. Did you use an aligner that is splice aware and use appropriate settings for it?
      Hi, GenoMax: Thanks for your advices. The specialist in the Bioinformatics service helped us with the data analysis. So the setting for those data analysis should be fine. The software used for seq data analysis is Partek flow. That worked good for our last programs.
      I would take samples to check using NCBI blast like you adviced.

      Comment

      • nucacidhunter
        Jafar Jabbari
        • Jan 2013
        • 1250

        #4
        Originally posted by lilichen View Post
        Hi, Everybody:

        We just completed mRNA seq for some human cells bulk samples.
        The QC for those seq data is good. But when we run the alignment for those samples, super low alignment rate come out ( ~50%). We built those lib samples by the pico-input stranded mRNA prep kit from Clontech.

        Is there any body have experience for this wired low alignment rate issue?
        Is there something wrong about the quality of original samples? or lib prep process? or seq running process?

        Any advice would be appreciated.
        Alignment rate to genome should be over 80% for libraries prepared with this kit.

        Comment

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