Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Demultiplexing combinatorial barcodes from paired end data

    Hey, I've been trying to figure out how to demultiplex paired-end 250 miseq data that has three different barcodes.

    The samples all come from 96 well plates. I have two 5' barcodes representing plate number as well as plate column. These two barcodes are linked via a common adapter sequence. I then have one 3' barcode that represents the plate column.

    I am fairly sure I would be able to demultiplexing the data in 2 rounds in which I first demultiplex based upon each plate/column combination, and then demultiplex the result based upon the 3' barcode.

    This seems fairly cumbersome as I have 2880 unique samples. Is there some sort of software in which I can provide simply the three unique barcodes, and then demultiplex in one step?

    Also, I usually use the A5Pipeline (https://code.google.com/p/ngopt/wiki/A5PipelineREADME) to error correct sequence reads, remove Illumina adapter sequences, and assemble the paired-reads. Would I be able to assemble the reads using A5 and then demultiplex the data, or do I have to run the pipeline on each individual sample after first demultiplexing. Thanks!

  • #2
    Does anyone have experience with combinatorial barcodes?

    Comment


    • #3
      How long are these barcodes? It may be possible to write some custom code to do this in one step but without seeing what you reads look like (or a good schematic) no one is going to be able to help. It may be best to find someone locally who can work with you interactively.

      If the A5Pipeline changes the context of the barcodes it will make things complicated. You may have to run the pipeline post demultiplexing.

      Comment


      • #4
        This will do it https://code.google.com/p/jmhc/

        Comment


        • #5
          Originally posted by JackieBadger View Post
          Can you import fastq files? Description states that it operates on fasta files (internally?). I don't think this will do 3 barcodes in a single pass.

          Comment


          • #6
            use skewer

            Hi ddelalca,
            You may use skewer for this purpose. An example command line is as follows:
            Code:
            skewer -x V3-forward.txt -y V4-reverse.txt --mode ap -t 4 ampliconReads-pair1.fastq ampliconReads-pair2.fastq assigned/
            If you only use some of the combinations, you may specify the matrix by -M as well.
            Good luck!
            Attached Files

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Essential Discoveries and Tools in Epitranscriptomics
              by seqadmin


              The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
              Yesterday, 07:01 AM
            • 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

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 04-11-2024, 12:08 PM
            0 responses
            39 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 10:19 PM
            0 responses
            41 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 09:21 AM
            0 responses
            35 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-04-2024, 09:00 AM
            0 responses
            55 views
            0 likes
            Last Post seqadmin  
            Working...
            X