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  • ttkuaile
    Junior Member
    • Sep 2008
    • 4

    #1

    paired-end run failed in pipeline v1.3.2

    During our first paired-end run in new version of pipeLine (v1.3.2), the image analysis and base call step passed, but the Gerald step failed to complete. In this run, the two reads of a pair have been stored into two separate RUN Folders. I used the Goat command to specify the two run folders. Do you have any idea or suggestion regarding this problem?

    The goat command, Gerald config file and error message are shown as follows:

    **********BEGIN PIPELINE COMMAN**********
    /opt/GAPipeline-1.3.2/bin/goat_pipeline.py
    /home/researchers/RunAnalysis/flowcell0014_1/Images
    /home/researchers/RunAnalysis/flowcell0014_2/Images
    --with-prb --with-sig2 --with-seq --with-qhg --with-qval --
    GERALD=/home/researchers/RunAnalysis/flowcell0014_1/pair_gerald_config_rs
    un.txt --control-lane=4 --make

    then cd to /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/

    run "make -j8 recursive"
    ********** END COMMAND*****************


    ***********BEGIN GERALD CONFIG FILE******
    4:ELAND_GENOME home/researchers/RunAnalysis/eland_genomes/phiX
    1235678:ELAND_GENOME
    /home/researchers/RunAnalysis/eland_genomes/Plasmodium_falciparum
    1235678:ANALYSIS eland_pair
    USE_BASES all
    ELAND_MULTIPLE_INSTANCES 8
    *********End CONFIG FILE *************************


    **********BEGIN ERROR MESSAGE **********
    /opt/GAPipeline-1.3.2/bin/legacyMakeQseqs.pl --orig_read_lengths 26:26 --
    qseq_suffix _qseq.txt.tmp --bustard_path
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers \
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_0001_seq.txt \
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_0001_qhg.txt \
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_0001_1_qcal.txt
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_0001_2_qcal.txt \
    && mv /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_1_0001_qseq.txt.tmp
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_1_0001_qseq.txt && mv
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_2_0001_qseq.txt.tmp
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_2_0001_qseq.txt \
    && echo `date` >
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_0001_qseqs.txt \
    && touch /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_1_0001_qseq.txt && touch
    /home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_2_0001_qseq.txt
    Unexpected runfolder directory name format at /opt/GAPipeline-
    1.3.2/bin/legacyMakeQseqs.pl line 73.
    make: *** [/home/researchers/RunAnalysis/flowcell0014_1/Data/C1-
    52_Firecrest1.3.2_14-04-2009_researchers/Bustard1.3.2_14-04-
    2009_researchers/s_3_0001_qseqs.txt] Error 255

    **********END ERROR MESSAGE*******************
  • cbrennan
    Member
    • Dec 2008
    • 28

    #2
    You shouldn't give it the "Images" folder -- just the top level, like you would for a single-read

    try:

    /opt/GAPipeline-1.3.2/bin/goat_pipeline.py
    /home/researchers/RunAnalysis/flowcell0014_1/
    /home/researchers/RunAnalysis/flowcell0014_2/
    --with-prb --with-sig2 --with-seq --with-qhg --with-qval --
    GERALD=/home/researchers/RunAnalysis/flowcell0014_1/pair_gerald_config_rs
    un.txt --control-lane=4 --make

    Christine
    Christine Brennan
    UM DNA Sequencing Core
    Ann Arbor, MI 48109

    [email protected]

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