Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • amos bank-transact show err

    Anyone tell me why ?

    running:

    bank-transact -c -b S1-S2.bnk -m S1-S2.afg

    log file show:

    AFG ..ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:1, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:2, message ignored
    ERROR: Sequence and quality lengths disagree
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:4, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:5, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:6, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:7, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:8, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:9, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:10, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:11, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:12, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:13, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:14, message ignored
    ERROR: Sequence and quality lengths disagree
    could not parse 'RED' message with iid:15, message ignored
    .
    .
    .
    .
    .
    .
    Last edited by bah; 02-22-2011, 01:35 PM.

  • #2
    afg file :

    {RED
    iid:8680569
    eid:ChrX_ctg150561
    seq:
    CTAGCCTCTGTACCTTTGCAGTAATTTAAAGTGTTAGCCAATGTGAGCATTCTAAGTATG
    TAATTCTCTTTCTGTGTCATTTGGACTATTCCAATACTCGGTGTGTCAGTAAACGTTGTA
    AAATTGTCTT
    .
    qlt:
    NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
    NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
    NNNNNNNNNN
    .
    frg:24678678
    clr:0,130
    }

    Comment


    • #3
      Did you changed the iid?? Perhaps that is the error when you're running the bank-transact. The programm not founded the iid to execute the parsing. Change the iid by 1, 2, 3, and so on. A little script in PERL can handle with this. But what is the size of the afg file?? The assembly file was generated by what assembler??


      Best regards,
      André

      Comment


      • #4
        yes, you are right. Each read name in the fasta file have two whitespace which lead to err. I had renamed them , then reproduced AFG file and the err was disappear.
        Thanks
        Hengxing

        Comment


        • #5
          We're welcome

          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...
            Yesterday, 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, 04-11-2024, 12:08 PM
          0 responses
          57 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          53 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          45 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          55 views
          0 likes
          Last Post seqadmin  
          Working...
          X