Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • tonybert
    Member
    • Aug 2012
    • 38

    #1

    GNU parallel + usearch piping

    Greetings, I am wondering if anyone knows how to pipe sequence data into usearch. I am trying to use GNU parallel to break-up up and distribute multiple smaller ublast jobs over our small server. I can do this with regular blast, but i get fatal errors when i try it with usearch-ublast.

    cat CAM_SMPL_001754_RMRNA_derep.fasta | parallel --block 100k --recstart '>' --pipe /public2/Tony/usearch -db /public2/Tony/CAMERA/RefSeqMicrobial/microbial.nonredundant.all.udb -top_hits_only -threads 16 -blast6out DATA

    Any suggestions would be helpful. thanks.
  • tange
    Junior Member
    • Feb 2013
    • 7

    #2
    Given: usearch -cluster_fast seqs.fasta -id 0.9 -centroids nr.fasta

    You can do:

    cat CAM_SMPL_001754_RMRNA_derep.fasta | parallel --block 100k --recstart '>' --pipe "cat > {#}; usearch -cluster_fast {#} -id 0.9 -centroids {#}.out; cat {#}.out; rm {#} {#}.out"

    Comment

    • tonybert
      Member
      • Aug 2012
      • 38

      #3
      Yes, this works for cluster_fast, but its blast I am really after. thanks,

      Comment

      • tange
        Junior Member
        • Feb 2013
        • 7

        #4
        I am no expert in usearch, but if you show the command line you would run to do it without GNU Parallel, then I might be able to help you parallelize it.

        Comment

        • tonybert
          Member
          • Aug 2012
          • 38

          #5
          thanks, below is the usearch command I would like to pipe;

          usearch -ublast ./454reads.fa -db ./RefSeqmicrobes.udb -evalue 1e-5 -top_hits_only -blast6out ./454reads_refseq_results

          Comment

          • tange
            Junior Member
            • Feb 2013
            • 7

            #6
            Extremely similar to the cluster_fast command:

            cat CAM_SMPL_001754_RMRNA_derep.fasta | parallel --block 100k --recstart '>' --pipe "cat > {#}; usearch -ublast ./{#} -db ./RefSeqmicrobes.udb -evalue 1e-5 -top_hits_only -blast6out ./{#}.out; cat {#}.out; rm {#} {#}.out"

            Comment

            • GisleVestergaard
              Junior Member
              • Sep 2014
              • 2

              #7
              Usearch has annoying default stdout output

              Originally posted by tange View Post
              Given: usearch -cluster_fast seqs.fasta -id 0.9 -centroids nr.fasta

              You can do:

              cat CAM_SMPL_001754_RMRNA_derep.fasta | parallel --block 100k --recstart '>' --pipe "cat > {#}; usearch -cluster_fast {#} -id 0.9 -centroids {#}.out; cat {#}.out; rm {#} {#}.out"
              This works very well, except for the fact that usearch (even using -quiet) will print 6 lines to stdout!
              usearch v7.0.1090_i86linux32, 4.0Gb RAM (32.5Gb total), 8 cores
              (C) Copyright 2013 Robert C. Edgar, all rights reserved.


              Licensed to: [email protected]

              The best solution I have found is to add:
              grep -E "^>|^[A,C,G,T]" > tyt

              Comment

              • tange
                Junior Member
                • Feb 2013
                • 7

                #8
                Originally posted by GisleVestergaard View Post
                This works very well, except for the fact that usearch (even using -quiet) will print 6 lines to stdout!
                usearch v7.0.1090_i86linux32, 4.0Gb RAM (32.5Gb total), 8 cores
                (C) Copyright 2013 Robert C. Edgar, all rights reserved.


                Licensed to: [email protected]

                The best solution I have found is to add:
                grep -E "^>|^[A,C,G,T]" > tyt
                Would this work with GNU Parallel 20140822:

                parallel --pipepart -a CAM_SMPL_001754_RMRNA_derep.fasta --block 100k --recstart '>' --cat "usearch -cluster_fast {} -id 0.9 -centroids {#}.out; tail -n +7 {#}.out; rm {#}.out"

                Comment

                • GisleVestergaard
                  Junior Member
                  • Sep 2014
                  • 2

                  #9
                  Originally posted by tange View Post
                  Would this work with GNU Parallel 20140822:

                  parallel --pipepart -a CAM_SMPL_001754_RMRNA_derep.fasta --block 100k --recstart '>' --cat "usearch -cluster_fast {} -id 0.9 -centroids {#}.out; tail -n +7 {#}.out; rm {#}.out"
                  Yes, this works and is faster than sed. Thanks!

                  Comment

                  Latest Articles

                  Collapse

                  • SEQadmin2
                    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                    by SEQadmin2



                    CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                    Despite this, “CRISPR helped turn genome editing from a specialized technique into
                    ...
                    07-31-2026, 11:01 AM
                  • SEQadmin2
                    Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                    by SEQadmin2


                    Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                    The systematic characterization of the human proteome has
                    ...
                    07-20-2026, 11:48 AM

                  ad_right_rmr

                  Collapse

                  News

                  Collapse

                  Topics Statistics Last Post
                  Started by SEQadmin2, 08-06-2026, 07:41 AM
                  0 responses
                  23 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 08-03-2026, 10:13 AM
                  0 responses
                  38 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-31-2026, 02:55 AM
                  0 responses
                  43 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 07-24-2026, 12:17 PM
                  0 responses
                  26 views
                  0 reactions
                  Last Post SEQadmin2  
                  Working...