Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Illumina Pipeline Version

    Hi!

    I'm digging through our old archives to convert all the *_sequence.txt files into .bam files using Picard tools to save disk space. I know that before Pipeline version 1.3 different quality scores were used, but now I'm wondering how to find out which version of the pipeline was used for a specific run? Is it the same number that is used in the path, e.g. version 1.5 for .../Bustard1.5.0_16-10-2009_seq/...? And when (so which month/year) has version 1.3 been published?

    Thanks!

    Thomas

  • #2
    See also http://seqanswers.com/forums/showthread.php?t=8895 for more recent changes to be aware of.

    Comment


    • #3
      If you look in the config.xml file in your GERALD directory it contains a load of useful information, including the full path to the program used for the processing. If you've used the normal methods of installing illumina pipelines then this will contain the pipeline version used.

      Comment


      • #4
        Ah, ok. Thanks! So for instance the entry:
        <BIN_DIR>/usr/local/packages/solexa-pipeline/GAPipeline-1.5.0/bin/../bin</BIN_DIR>
        should mean that this run was analysed using version 1.5?

        Comment


        • #5
          Originally posted by t.wieland View Post
          Ah, ok. Thanks! So for instance the entry:
          <BIN_DIR>/usr/local/packages/solexa-pipeline/GAPipeline-1.5.0/bin/../bin</BIN_DIR>
          should mean that this run was analysed using version 1.5?
          That would seem to be the case in our run folders. It might break down if you'd added the pipeline bin folder to the path and not specified the full path to Bustard/Gerald etc, but since we've never done that I'm not sure what would end up in BIN_DIR in those cases.

          Comment


          • #6
            Ok, unfortunately in many cases these paths don't include the version number. Any other ideas? Does anybody know what Picard tools FastqToSam does when it finds a quality value thats out of range? Because if it would throw an Exception, we could just work it out in a kind of trial-and-error strategy.

            Comment


            • #7
              You could run the files through fastqc which will detect the encoding used. That would then let you pass on the appropriate flags to picard to do the conversion.

              Comment


              • #8
                Hi Simon,

                thanks for this suggestion. I'm running it right now to detect the encoding and so far it found the values "Illumina 1.5" and "Sanger / Illumina 1.9". Now I'm wondering which are the possible encoding values fastqc produces and which of these values correspond to the old Illumina encoding and which to the new one?

                Comment


                • #9
                  Originally posted by t.wieland View Post
                  Hi Simon,

                  thanks for this suggestion. I'm running it right now to detect the encoding and so far it found the values "Illumina 1.5" and "Sanger / Illumina 1.9". Now I'm wondering which are the possible encoding values fastqc produces and which of these values correspond to the old Illumina encoding and which to the new one?
                  The set of encodings it can detect, and the associated offset values are:
                  • Illumina <1.3 (59)
                  • Illumina 1.3 (64)
                  • Illumina 1.5 (64)
                  • Sanger / Illumina 1.9 (33)


                  If you're converting to SAM/BAM you'll need to convert anything which isn't Sanger/Illumina 1.9.

                  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
                  30 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 04-10-2024, 10:19 PM
                  0 responses
                  32 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 04-10-2024, 09:21 AM
                  0 responses
                  28 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 04-04-2024, 09:00 AM
                  0 responses
                  53 views
                  0 likes
                  Last Post seqadmin  
                  Working...
                  X