Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ardmore
    Member
    • Jun 2011
    • 51

    #1

    Wild output

    Hello, I am tring to generate the consensus sequence by using command
    Code:
    samtools pileup -cf ref.fa aln.bam | samtools.pl pileup2fq -D100 > cns.fastq
    However I found that in the output file there are a lot wild characters such as

    Code:
    ~~~~~~~~~~~~~~~~~{~~~~~~~~o~~~~~~~~~~~~{~~~{~~~{{{x{{{~{{xfr
    uuurru{{xux{{{{{{{~~~{~~~~~~~f~~n~~~~~~~~~~~~~~~~~~~~~~~~~~~
    ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~{c{{~x~~~~l{
    ~~~~~~~~~~~~~xxxxxuuuroloooooollolfffiiifffcfffff``Mc]]]``]`
    ]`````````cffiifiiiiillllllilllllllill3liiiiiffffffff```````
    ``]]]]]]]]]]ZZZWWWTTQQNNNNNQTTQEQKEKHEEEEEBBBEEHHHHKKQTWWWWW
    QTW]`fiiNllilillllliloolollrrrrrrrrrruuuux{{{{{{~~~~~~~~~~~~
    So what is wrong?
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    You made a fastq, and it has quality scores, exactly like a fastq is supposed to have.

    If you understood the programs you are running, you would not be so surprised when they function exactly as they are supposd to.

    Comment

    • ardmore
      Member
      • Jun 2011
      • 51

      #3
      I am not strong on perl. So could you please advise me the details?
      How can I get the right sequence?

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        Originally posted by ardmore View Post
        I am not strong on perl.
        You're question has nothing to do with perl.

        Originally posted by ardmore View Post
        So could you please advise me the details?
        How can I get the right sequence?
        swbarnes2 gave you enough to figure it out:
        Originally posted by swbarnes2 View Post
        You made a fastq, and it has quality scores, exactly like a fastq is supposed to have.
        So ardmore, did you actually read his reply? Have you looked at the fastq file format? Have you bothered looking up what a quality score is?

        Comment

        • ardmore
          Member
          • Jun 2011
          • 51

          #5
          Okay. Can we read quality scores based on the fasta file?
          I google search but no clue.

          Comment

          • dpryan
            Devon Ryan
            • Jul 2011
            • 3478

            #6
            Originally posted by ardmore View Post
            Okay. Can we read quality scores based on the fasta file?
            I google search but no clue.
            That's not a coherent question. Why are you asking about fasta files when you have a fastq file? I wonder if your problem is misreading fastq as fasta.

            Comment

            • ardmore
              Member
              • Jun 2011
              • 51

              #7
              Oop. I did make a mistake. I misread the command. My goal is to get a fasta file. I didn't pay attention to it.

              So how can I get the fasta file?
              Convert fastq to fasta?
              or using mpileup?
              Because I got an error by
              http://biostar.stackexchange.com/que...ric-in-numeric
              I am sad.

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                by SEQadmin2



                Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                ...
                10-14-2026, 09:55 AM
              • SEQadmin2
                New Genomics Technologies Take Aim at Long-Standing Limits
                by SEQadmin2


                Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

                We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
                ...
                09-28-2026, 10:25 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, Yesterday, 11:13 AM
              0 responses
              17 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, Yesterday, 10:48 AM
              0 responses
              18 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-15-2026, 10:52 AM
              0 responses
              36 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              42 views
              0 reactions
              Last Post SEQadmin2  
              Working...