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  • litali
    Member
    • Jul 2010
    • 78

    16s analysis for one sample

    How can I perform an analysis for one sample 454 16s sequences?
    I thought to use qiime, but there are steps relating to the barcodes. I don't have barcodes in my sequences, only primers.
  • rhinoceros
    Senior Member
    • Apr 2013
    • 372

    #2
    You don't need barcodes for QIIME. QIIME's documentation is IMO rather poor but you can read about non-barcoded input e.g. here.
    savetherhino.org

    Comment

    • Ciaran
      Junior Member
      • Sep 2011
      • 9

      #3
      Qiime, is a series of scripts that forms a pipeline.
      Just start the pipeline from the step post demultiplexing.

      qiime

      Comment

      • litali
        Member
        • Jul 2010
        • 78

        #4
        qiime for one sample

        but if I skip the demultiplexing step how will the linkerprimer be removed? I understand that it is the demultiplexing step that usually performs it..

        Comment

        • rhinoceros
          Senior Member
          • Apr 2013
          • 372

          #5
          Originally posted by litali View Post
          but if I skip the demultiplexing step how will the linkerprimer be removed? I understand that it is the demultiplexing step that usually performs it..
          But why would you skip it? If your libraries don't have barcodes then you simply specify this for split_libraries.py with -b 0 (=barcode length is zero)
          savetherhino.org

          Comment

          • litali
            Member
            • Jul 2010
            • 78

            #6
            qiime for one sample

            Originally posted by rhinoceros View Post
            But why would you skip it? If your libraries don't have barcodes then you simply specify this for split_libraries.py with -b 0 (=barcode length is zero)
            In previous response Ciaran suggested that I should start the pipeline from the step post demultiplexing, tha's why I asked that if I start post demultiplexing, I actually start with the Pick otus step , so the primers are left. My library is only one sample and the reads begin from the primer (without the adaptor) so maybe it is ok?

            Comment

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