Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • srma-0.1.8 error - Cannot check readability of null file.

    Trying to use srma for the first time, version 0.1.8. Here's the invocation:

    Code:
    java -jar ./srma-0.1.8.jar INPUT=x.sam REFERENCE=chr22.fa OUTPUT=x.out
    ...and the output:

    Code:
    [Sat Oct 09 05:26:25 UTC 2010] srma.SRMA REFERENCE=chr22.fa    OFFSET=20 MIN_MAPQ=0 MINIMUM_ALLELE_PROBABILITY=0.1 MINIMUM_ALLELE_COVERAGE=3 MAXIMUM_TOTAL_COVERAGE=100 CORRECT_BASES=false USE_SEQUENCE_QUALITIES=true QUIET_STDERR=false MAX_HEAP_SIZE=8192 MAX_QUEUE_SIZE=65536 NUM_THREADS=1 TMP_DIR=/tmp/ec2-user VERBOSITY=INFO QUIET=false VALIDATION_STRINGENCY=STRICT COMPRESSION_LEVEL=5 MAX_RECORDS_IN_RAM=500000 CREATE_INDEX=false
    java.lang.IllegalArgumentException: Cannot check readability of null file.
    	at net.sf.picard.io.IoUtil.assertFileIsReadable(IoUtil.java:48)
    	at net.sf.picard.reference.FastaSequenceIndex.<init>(FastaSequenceIndex.java:54)
    	at net.sf.picard.reference.IndexedFastaSequenceFile.<init>(IndexedFastaSequenceFile.java:95)
    	at srma.SRMA.doWork(SRMA.java:125)
    	at net.sf.picard.cmdline.CommandLineProgram.instanceMain(CommandLineProgram.java:160)
    	at srma.SRMA.main(SRMA.java:92)
    Please report bugs to [email protected]
    ... and yes, the inputs exist:

    Code:
    ls -l x.sam chr22.fa 
    -rw-rw-r-- 1 ec2-user ec2-user 50685268 Oct  9 05:23 chr22.fa
    -rw-rw-r-- 1 ec2-user ec2-user    25181 Oct  9 05:32 x.sam
    Help appreciated.

  • #2
    Originally posted by allenday View Post
    Trying to use srma for the first time, version 0.1.8. Here's the invocation:

    Code:
    java -jar ./srma-0.1.8.jar INPUT=x.sam REFERENCE=chr22.fa OUTPUT=x.out
    ...and the output:

    Code:
    [Sat Oct 09 05:26:25 UTC 2010] srma.SRMA REFERENCE=chr22.fa    OFFSET=20 MIN_MAPQ=0 MINIMUM_ALLELE_PROBABILITY=0.1 MINIMUM_ALLELE_COVERAGE=3 MAXIMUM_TOTAL_COVERAGE=100 CORRECT_BASES=false USE_SEQUENCE_QUALITIES=true QUIET_STDERR=false MAX_HEAP_SIZE=8192 MAX_QUEUE_SIZE=65536 NUM_THREADS=1 TMP_DIR=/tmp/ec2-user VERBOSITY=INFO QUIET=false VALIDATION_STRINGENCY=STRICT COMPRESSION_LEVEL=5 MAX_RECORDS_IN_RAM=500000 CREATE_INDEX=false
    java.lang.IllegalArgumentException: Cannot check readability of null file.
    	at net.sf.picard.io.IoUtil.assertFileIsReadable(IoUtil.java:48)
    	at net.sf.picard.reference.FastaSequenceIndex.<init>(FastaSequenceIndex.java:54)
    	at net.sf.picard.reference.IndexedFastaSequenceFile.<init>(IndexedFastaSequenceFile.java:95)
    	at srma.SRMA.doWork(SRMA.java:125)
    	at net.sf.picard.cmdline.CommandLineProgram.instanceMain(CommandLineProgram.java:160)
    	at srma.SRMA.main(SRMA.java:92)
    Please report bugs to [email protected]
    ... and yes, the inputs exist:

    Code:
    ls -l x.sam chr22.fa 
    -rw-rw-r-- 1 ec2-user ec2-user 50685268 Oct  9 05:23 chr22.fa
    -rw-rw-r-- 1 ec2-user ec2-user    25181 Oct  9 05:32 x.sam
    Help appreciated.
    There is a potential bug in Picard that I am investigating right now giving this cryptic error message. Try running "samtools faidx chr22.fa". You need to index the reference FASTA file.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      04-22-2024, 07:01 AM
    • 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

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, Today, 08:47 AM
    0 responses
    10 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    60 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    59 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    53 views
    0 likes
    Last Post seqadmin  
    Working...
    X