Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • silentio
    Junior Member
    • Jul 2012
    • 4

    #1

    BWA aligned sam file missing "QNAME" format

    Hi all,
    I am using BWA to align pair-end read to hg19 genome.
    Command line are as follows:

    bwa aln $ref_dir/hg19 -t 4 $work_dir/${sample}_human_1.fastq.gz > $sai_dir/${sample}_1.sai
    bwa aln $ref_dir/hg19 -t 4 $work_dir/${sample}_human_2.fastq.gz > $sai_dir/${sample}_2.sai
    bwa sampe -r "@RG\tID:$sample\tLB:$sample\tSM:$sample\tPL:ILLUMINA" $ref_dir/hg19 $sai_dir/${sample}_1.sai $sai_dir/${sample}_2.sai $work_dir/${sample}_human_1.fastq.gz $work_dir/${sample}_human_2.fastq.gz | gzip > $sam_dir/$sample.sam.gz


    However, some lines in the generated sam file are missing the "QNAME" field, starting from the FLAG field directly. As a result, the downstream command such as converting sam to bam cannot be done, giving information such as "Error parsing text SAM file. Not enough fields".

    I wonder if it is the problem of bwa, or the problem of my fastq files?

    Thanks in advance for your suggestions!
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    Is gzipping the .sam really the right way to make a bam?

    Try

    Code:
    bwa sampe all that stuff | samtools view -bSh - > sample.bam

    Comment

    • maubp
      Peter (Biopython etc)
      • Jul 2009
      • 1544

      #3
      Originally posted by silentio View Post
      However, some lines in the generated sam file are missing the "QNAME" field, starting from the FLAG field directly. As a result, the downstream command such as converting sam to bam cannot be done, giving information such as "Error parsing text SAM file. Not enough fields".

      I wonder if it is the problem of bwa, or the problem of my fastq files?
      Can you show us some of these bad SAM lines? Perhaps they have empty strings as the QNAME (which is bad), in which case can you look at the FASTQ file to see if that had records without an identifier?

      Comment

      • silentio
        Junior Member
        • Jul 2012
        • 4

        #4
        I found the problem. It is because of the fastq files. Normally a fastq file starts with '"@" in the ID line. However, before running bwa, I used another software to do some preprocessing, which removed the "@". After adding "@" back, all return to normal.
        Thanks for your reply anyway!

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM
        • 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

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 07-31-2026, 02:55 AM
        0 responses
        15 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        15 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-23-2026, 11:41 AM
        0 responses
        13 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-20-2026, 11:10 AM
        0 responses
        24 views
        0 reactions
        Last Post SEQadmin2  
        Working...