Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 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.

  • #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


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

      qiime

      Comment


      • #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


        • #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


          • #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

            Latest Articles

            Collapse

            • seqadmin
              Current Approaches to Protein Sequencing
              by seqadmin


              Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
              04-04-2024, 04:25 PM
            • seqadmin
              Strategies for Sequencing Challenging Samples
              by seqadmin


              Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
              03-22-2024, 06:39 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 04-11-2024, 12:08 PM
            0 responses
            25 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 10:19 PM
            0 responses
            28 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 09:21 AM
            0 responses
            24 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-04-2024, 09:00 AM
            0 responses
            52 views
            0 likes
            Last Post seqadmin  
            Working...
            X