Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Bio.X2Y
    Member
    • Apr 2010
    • 46

    samtools picard SamFormatConverter

    Hi,

    I'm trying to run SamFormatConverter to convert a BAM to a SAM, and I'm getting an error (see below).

    The text suggests that samtools is trying to parse my BAM as a SAM. However, the file is definitely a BAM, has a '.bam' extension, and appears to have the necessary "magic number" at the top.

    Any ideas if I might be doing something wrong?

    Thanks!

    Command:
    java -jar <location>/SamFormatConverter.jar I=in.bam O=out.sam

    Head in.bam:
    BAM?@HD VN:1.0 GO:none SO:unsorted
    @SQ SN:chrM LN:16571 AS:HG18 UR:/seq/references/Homo_sapiens_assembly18/v0/Homo_sapiens_assembly18.fasta M5:d2ed829b8a1628d16cbeee88e88e39eb SP:Homo sapiens

    Exception:
    Exception in thread "main" net.sf.samtools.SAMFormatException: Error parsing text SAM file. Not enough fields; Line 1
    Line: BAM?@HD VN:1.0 GO:none SO:unsorted
    at net.sf.samtools.SAMTextReader.reportFatalErrorParsingLine(SAMTextReader.java:169)
    at net.sf.samtools.SAMTextReader.access$400(SAMTextReader.java:40)
    at net.sf.samtools.SAMTextReader$RecordIterator.parseLine(SAMTextReader.java:261)
    at net.sf.samtools.SAMTextReader$RecordIterator.next(SAMTextReader.java:224)
    at net.sf.samtools.SAMTextReader$RecordIterator.next(SAMTextReader.java:196)
    at net.sf.picard.sam.SamFormatConverter.doWork(SamFormatConverter.java:64)
    at net.sf.picard.cmdline.CommandLineProgram.instanceMain(CommandLineProgram.java:150)
    at net.sf.picard.sam.SamFormatConverter.main(SamFormatConverter.java:72)
  • bh1
    Junior Member
    • Feb 2011
    • 1

    #2
    Hi,
    Did you figure a solution for this problem? I'm getting exactly the same error message.
    thanks.

    Comment

    • Richard Finney
      Senior Member
      • Feb 2009
      • 701

      #3
      Validation_stringency=lenient

      Try VALIDATION_STRINGENCY=LENIENT in the java invocation.

      Example:

      java-Xmx67T -jar wherever/SamTowhatevernameis.jar \
      VALIDATION_STRINGENCY=LENIENT \ INPUT=uncle.sam O=nephew.sam


      That might shut up the error message and get Picard to accept the input.

      Comment

      • bw.
        Member
        • Mar 2012
        • 21

        #4
        In this case the issue is probably the
        "BAM?" on the 1st line in front of "@HD VN:1.0 GO:none SO:unsorted"
        I would try deleting it.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
          by SEQadmin2



          Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
          ...
          07-09-2026, 11:10 AM
        • SEQadmin2
          Cancer Drug Resistance: The Lingering Barrier to Rising Survival
          by SEQadmin2



          Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

          There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
          07-08-2026, 05:17 AM
        • GATTACAT
          Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by GATTACAT
          Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
          07-01-2026, 11:43 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 07-13-2026, 10:26 AM
        0 responses
        21 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-09-2026, 10:04 AM
        0 responses
        32 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-08-2026, 10:08 AM
        0 responses
        20 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-07-2026, 11:05 AM
        0 responses
        34 views
        0 reactions
        Last Post SEQadmin2  
        Working...