Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Fastq to sam issues

    So, I've been trying to convert my .fastq files to .sam files in order to use scripture to align the reads without using a reference genome. To do this I've installed picard (along with samtools and the rest of the men's wear suite), however when I try to run the FastqToSam function I get an error I do not understand.

    My input:

    java -Xmx2g -jar FastqToSam.jar FASTQ=file1.fastq FASTQ2=file2.fastq OUTPUT=file3.sam PREDICTED_INSERT_SIZE=xx QUALITY_FORMAT=Illumina SAMPLE_NAME=file4

    and the error message:

    Exception in thread "main" java.lang.IllegalArgumentException: Cannot encode phred score: 253
    at net.sf.samtools.SAMUtils.phredToFastq(SAMUtils.java:255)
    at net.sf.samtools.SAMUtils.phredToFastq(SAMUtils.java:243)
    at net.sf.samtools.SAMUtils.phredToFastq(SAMUtils.java:229)
    at net.sf.samtools.SAMRecord.getBaseQualityString(SAMRecord.java:239)
    at net.sf.samtools.SAMTextWriter.writeAlignment(SAMTextWriter.java:100)
    at net.sf.samtools.SAMFileWriterImpl.close(SAMFileWriterImpl.java:178)
    at net.sf.picard.sam.FastqToSam.doUnpaired(FastqToSam.java:133)
    at net.sf.picard.sam.FastqToSam.doWork(FastqToSam.java:111)
    at net.sf.picard.cmdline.CommandLineProgram.instanceMain(CommandLineProgram.java:156)
    at net.sf.picard.sam.FastqToSam.main(FastqToSam.java:106)


    Can anyone help me with this?

    Is this something to do with installing ant? or SAM-JDK? I can't really figure it out and am working on a Mac OS X with all the developer tools installed. Please help.

  • #2
    Hi,

    It seems that the problem might be due to some illegale or out of range phred scores as the error message says "Cannot encode phred score: 253". You might want to have a look here http://en.wikipedia.org/wiki/FASTQ_format and check your FASTQ file if there are some strange quality score outliers or recheck the QUALITY_FORMAT option of FastqToSam.

    Cheers, D.

    Comment

    Latest Articles

    Collapse

    • 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
    • seqadmin
      Strategies for Sequencing Challenging Samples
      by seqadmin


      Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
      03-22-2024, 06:39 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    24 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    25 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    21 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    52 views
    0 likes
    Last Post seqadmin  
    Working...
    X