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  • 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?

  • #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


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

      Comment


      • #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


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

          Comment


          • #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


            • #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

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