Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Help with RSEM: how to change default phred33 to phred64

    Hi all,

    When I was using the RSEM to align my reads.fastq to my transcripts.fasta (trinityrnaseq_r2013-02-25/util/RSEM_util/run_RSEM_align_n_estimate.pl), I happened to see this:

    bowtie -q --phred33-quals -n 2 -e 99999999 -l 25 -I 1 -X 1000 --chunkmbs 200 -p 4 -a -m 200 -S TRANS -1

    But my fastq used phred64, so is there a way to change the default setting (phred33)? Does it affect much if I used the default setting?

    Thanks,
    He

  • #2
    It shouldn't matter much. But if you want to change the quality, you could download BBTools and do this:

    reformat.sh in=reads.fastq out=fixed.fastq qin=64 qout=33

    Comment


    • #3
      From the trinity page--


      # To pass additional parameters to rsem-calculate-expression,
      # type ' -- ' followed by additional pass-through params
      You could try <original command> --phred64-quals
      Other parameters can be passed in the same way.

      Comment


      • #4
        Hi Yueluo,
        I tried typing --phred64-quals behind my command (../run_RSEM_align_n_estimate.pl/ --transcripts) but it said: Unknown option: phred64-quals.
        He

        Comment


        • #5
          Brian,
          I will try it and see if it works.
          Thanks,
          He

          Comment


          • #6
            Well I guess you could follow what Brian suggested. But it is strange you can't use the '--phred64-quals' option as it is mentioned on both trinity's and RSEM's websites.

            Converting the phred-qual isn't too difficult, but it is time-consuming when you process large data sets and adds pressure to the system's I/O and storage -- which is a concern to myself and probably some others.

            Comment


            • #7
              Originally posted by yueluo View Post
              Converting the phred-qual isn't too difficult, but it is time-consuming when you process large data sets and adds pressure to the system's I/O and storage -- which is a concern to myself and probably some others.
              So you would think! But no, reformat.sh is extremely fast, clocked at over 500MB/s (note that a single HDD won't be able to deliver this). And you can pipe it, like this:

              reformat.sh in=reads.fq out=stdout.fq qin=64 qout=33 | someOtherProcess

              ...which will add no load to the system's I/O or storage, as long as the other process accepts stdin. For, you see, I am also concerned with these things!

              Comment


              • #8
                Good to hear Brian ! I'll give it a go soon and see how well that goes

                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
                18 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 04-10-2024, 10:19 PM
                0 responses
                22 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 04-10-2024, 09:21 AM
                0 responses
                16 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 04-04-2024, 09:00 AM
                0 responses
                47 views
                0 likes
                Last Post seqadmin  
                Working...
                X