Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sowmyai
    Member
    • Jan 2010
    • 27

    #1

    SAM tools output question

    Column 3 in SAM output format is supposed to be "the name of the reference sequence where alignment occurs" - as per documentation.
    If I see an asterisk (*) in column 3, what does that indicate ? Did the read not map at all ?
  • ForeignMan
    Member
    • Jun 2010
    • 20

    #2
    Hi,

    hope you don't mind if I'll make it easy for myself and pass over to the the SAM Format Specification
    (you can download it via http://samtools.sourceforge.net/SAM1.pdf )

    "QNAME and FLAG are required for all alignments. If the mapping position of the query is not available, RNAME and CIGAR are set as *, and POS and MAPQ as 0. If the query is unpaired or pairing information is not available, MRNM equals *, and MPOS and ISIZE equal 0. SEQ and QUAL can both be absent, represented as a star *. If QUAL is not a star, it must be of the same length as SEQ."

    Thus, you're right and the read didn't map. Hope it helps.

    Comment

    • sowmyai
      Member
      • Jan 2010
      • 27

      #3
      Thank you. But that is for QNAME and FLAG, the first and second fields. I am talking about RNAME, the third field, which is supposed to contain the name of the reference sequence that the read mapped to. It makes sense that this field should be * if the read did not map to any reference, but I just wanted to be sure.

      Comment

      • misko
        Junior Member
        • Jun 2010
        • 7

        #4
        Hi,
        Was ForeignMan referring to this part of the note?,
        "If the mapping position of the query is not available, RNAME and CIGAR are set as *, and POS and MAPQ as 0."
        It does mention that RNAME can be '*', when the read did not map.

        Misko

        Comment

        • bpetersen
          Member
          • Mar 2010
          • 20

          #5
          I think the problem might also be different names used for your reference sequences in your reference and the sam header (or the origin of it). I've been using Bioscope and had the same problem when taking the samfile generated by Bioscope and converting it to bam with samtools. The problem for me was "chr1" in the reference and "Chr1" in the sam library file used to generate the sam header.
          But that would result in * everywhere in column 3, I don't know if that's the case with your data. Well, maybe this still helps.

          Comment

          • sowmyai
            Member
            • Jan 2010
            • 27

            #6
            Thanks guys. Sorry foreignman, I missed the RNAME part of your reply.

            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
              ...
              Yesterday, 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, Yesterday, 02:55 AM
            0 responses
            9 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            12 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-23-2026, 11:41 AM
            0 responses
            12 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...