Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • kga1978
    Senior Member
    • Nov 2010
    • 100

    #1

    Error in IlluminaBasecallsToSam.jar

    Hi All,

    I run the following command

    Code:
    java -Xmx2g -Dsnappy.disable=true -jar /idi/sabeti-scratch/kandersen/bin/picard/IlluminaBasecallsToSam.jar BASECALLS_DIR=/broad/hptmp/andersen/130130.C1E4YACXX/Data/Intensities/BaseCalls/ LANE=5 READ_STRUCTURE=101T8B101T LIBRARY_PARAMS=/idi/sabeti-data/kandersen/analysis/130130_sarah_rerun/_logs/library_params.txt SEQUENCING_CENTER=Broad RUN_BARCODE=C1E4YACXX NUM_PROCESSORS=4 ADAPTERS_TO_CHECK=PAIRED_END MAX_READS_IN_RAM_PER_TILE=100000 MAX_RECORDS_IN_RAM=100000 FORCE_GC=false
    but I keep getting the following error:

    Code:
    [Wed Jan 30 16:07:56 EST 2013] net.sf.picard.illumina.IlluminaBasecallsToSam BASECALLS_DIR=/broad/hptmp/andersen/130130.C1E4YACXX/Data/Intensities/BaseCalls LANE=5 RUN_BARCODE=C1E4YACXX SEQUENCING_CENTER=Broad READ_STRUCTURE=101T8B101T LIBRARY_PARAMS=/idi/sabeti-data/kandersen/analysis/130130_sarah_rerun/_logs/library_params.txt ADAPTERS_TO_CHECK=[INDEXED, DUAL_INDEXED, NEXTERA_V2, FLUIDIGM, PAIRED_END] NUM_PROCESSORS=4 FORCE_GC=false MAX_READS_IN_RAM_PER_TILE=100000 MAX_RECORDS_IN_RAM=100000    PLATFORM=illumina VERBOSITY=INFO QUIET=false VALIDATION_STRINGENCY=STRICT COMPRESSION_LEVEL=5 CREATE_INDEX=false CREATE_MD5_FILE=false
    [Wed Jan 30 16:07:56 EST 2013] Executing as andersen@node398 on Linux 2.6.18-194.8.1.el5 amd64; Java HotSpot(TM) 64-Bit Server VM 1.6.0_35-b10; Picard version: 1.84(1332)
    INFO	2013-01-30 16:07:56	IlluminaBasecallsToSam	DONE_READING STRUCTURE IS 101T8B101T
    [Wed Jan 30 16:07:56 EST 2013] net.sf.picard.illumina.IlluminaBasecallsToSam done. Elapsed time: 0.01 minutes.
    Runtime.totalMemory()=125435904
    FAQ:  http://sourceforge.net/apps/mediawiki/picard/index.php?title=Main_Page
    Exception in thread "main" java.lang.NullPointerException
    	at net.sf.samtools.util.StringUtil.join(StringUtil.java:54)
    	at net.sf.picard.illumina.IlluminaBasecallsToSam.populateWritersFromLibraryParams(IlluminaBasecallsToSam.java:962)
    	at net.sf.picard.illumina.IlluminaBasecallsToSam.initialize(IlluminaBasecallsToSam.java:839)
    	at net.sf.picard.illumina.IlluminaBasecallsToSam.doWork(IlluminaBasecallsToSam.java:754)
    	at net.sf.picard.cmdline.CommandLineProgram.instanceMain(CommandLineProgram.java:177)
    	at net.sf.picard.illumina.IlluminaBasecallsToSam.main(IlluminaBasecallsToSam.java:1038)
    I have tried different versions of the program, with and without 'snappy' and checked that all the required files are there (e.g. library_params.txt) and point to the correct directories, etc. Everything appears to be correct.

    Before this command I extract barcodes using:

    Code:
    java -Xmx2g -jar /seq/software/picard/1.465/bin/ExtractIlluminaBarcodes.jar BASECALLS_DIR=/broad/hptmp/andersen/130130.C1E4YACXX/Data/Intensities/BaseCalls/ LANE=5 READ_STRUCTURE=101T8B101T BARCODE_FILE=/idi/sabeti-data/kandersen/analysis/130130_sarah_rerun/_logs/barcodeData.5 METRICS_FILE=/idi/sabeti-data/kandersen/analysis/130130_sarah_rerun/_logs/barcode.metrics.txt MAX_MISMATCHES=0 MINIMUM_BASE_QUALITY=25 NUM_PROCESSORS=1
    which completes and generates bar-code files correctly (as far as I can tell).

    Any ideas what is going on here?

    Thanks

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
    ...
    10-14-2026, 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, 10-22-2026, 11:13 AM
0 responses
26 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
20 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
36 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
43 views
0 reactions
Last Post SEQadmin2  
Working...