Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • horvathdp
    Member
    • Dec 2011
    • 66

    #1

    Why is BBmap throwing java error

    Hi all,

    I have some myseq data that I want to clean up using bbmap. When I give the following command, I get this error. What is wrong? I am guessing it is having a problem with the sequence I downloaded from the vendor, but I can't figure out what the issue is. Help???

    ./bbduk.sh in1=Plate1_clean1_R1.fastq in2=Plate1_clean1_R2.fastq out1=Plate1_clean2_R1.fastq out2=Plate1_clean2_R2.fastq qtrim=rl trimq=20 minlen=70

    java -Djava.library.path=/home/dave/bbmap/jni/ -ea -Xmx103643m -Xms103643m -cp /home/dave/bbmap/current/ jgi.BBDukF in1=Plate1_clean1_R1.fastq in2=Plate1_clean1_R2.fastq out1=Plate1_clean2_R1.fastq out2=Plate1_clean2_R2.fastq qtrim=rl trimq=20 minlen=70
    Executing jgi.BBDukF [in1=Plate1_clean1_R1.fastq, in2=Plate1_clean1_R2.fastq, out1=Plate1_clean2_R1.fastq, out2=Plate1_clean2_R2.fastq, qtrim=rl, trimq=20, minlen=70]

    BBDuk version 35.82
    Initial:
    Memory: max=104150m, free=100346m, used=3804m

    Input is being processed as paired
    Started output streams: 0.025 seconds.
    Exception in thread "Thread-5" java.lang.AssertionError:
    Error in Plate1_clean1_R1.fastq, line 1046, with these 4 lines:
    GTTCGTCTCTACACTGACGACATGGTTCTACAGTCCATGTGAATACGAAGGGAAGCATTTTTTTTAAAAAGTAAATTGTTTTGTATACTGCAGTACTATGGGCTATGGTGAGACCAAGTCTCTGCTACCGTATGCGTCAGAAGATCGGAAT
    +
    >1>>1>AAFFDFEGGDAGEAEEE1FGHHHHHHHHHHHHHHHFHHHHHGCFGCF0E/1DFGHHGGGE1@G1AGHHHHHHHGHGEHBGHHHHHFFHHFHFG2BFFHHHHHF1101>?CFHHHHHFH1EG1FCFHHGH?EC/?11<CGHHG///
    @M00619:318:000000000-B4H7N:1:1101:17348:2448 1:N:0:ATCACGAT+TCTTTCCC

    at stream.FASTQ.quadToRead(FASTQ.java:722)
    at stream.FASTQ.toReadList(FASTQ.java:653)
    at stream.FastqReadInputStream.fillBuffer(FastqReadInputStream.java:111)
    at stream.FastqReadInputStream.hasMore(FastqReadInputStream.java:76)
    at stream.ConcurrentGenericReadInputStream$ReadThread.readLists(ConcurrentGenericReadInputStream.java:643)
    at stream.ConcurrentGenericReadInputStream$ReadThread.run(ConcurrentGenericReadInputStream.java:635)
    Exception in thread "Thread-6" java.lang.AssertionError:
    Error in Plate1_clean1_R2.fastq, line 1145, with these 4 lines:
    TCACGCTATGTACGGTAGCAGAGACTTGGTCTGGTTGCTTATTGGGTTACGGTTTGATTGTTGATTCGTGGTGGTACAACTTTAGTGACGGATGGTGATTGTTGTGATGGTAAGCTAAGGTCGTGTAGAACCATGTCGTCAGTGTCATAGC
    +
    1>>>AFAA?FFBGGCGGGFFGGHFBGHH1GGHHFDGGHFHHGHFFHFFGACFF/EEBDGFFDGFGHFEHEFACEEHHEHFFHH@GG12FFE/>E/F1@2GF@DGHF2221F2B>1B1B1FGHEE/?F12EDHAGEDGAFF//BBF2>FFF1
    @M00619:318:000000000-B4H7N:1:1101:14067:2496 2:N:0:ATCACGAT+TCTTTCCC

    at stream.FASTQ.quadToRead(FASTQ.java:722)
    at stream.FASTQ.toReadList(FASTQ.java:653)
    at stream.FastqReadInputStream.fillBuffer(FastqReadInputStream.java:111)
    at stream.FastqReadInputStream.hasMore(FastqReadInputStream.java:76)
    at stream.ConcurrentGenericReadInputStream$ReadThread.readLists(ConcurrentGenericReadInputStream.java:643)
    at stream.ConcurrentGenericReadInputStream$ReadThread.run(ConcurrentGenericReadInputStream.java:635)
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    Can you try running by specifying the memory by adding "-Xmx4g" to your command?

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
      by SEQadmin2



      Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

      Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
      ...
      Yesterday, 09:55 AM
    • SEQadmin2
      New Genomics Technologies Take Aim at Long-Standing Limits
      by SEQadmin2


      Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

      We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
      ...
      09-28-2026, 10:25 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 05:39 AM
    0 responses
    11 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-13-2026, 09:56 AM
    0 responses
    14 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-09-2026, 11:14 AM
    0 responses
    27 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 09-29-2026, 09:51 AM
    0 responses
    78 views
    0 reactions
    Last Post SEQadmin2  
    Working...