Unconfigured Ad

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

    #1

    Fastq to Fasta

    Hello I want to convert fastq to fasta, by google search I got a perl code.

    However my perl knowledge is almost zero, I don't know how to run this script. Do I need to input arguments for input or output file?
    Please give me an example.


    Thanks.
  • NicoBxl
    not just another member
    • Aug 2010
    • 264

    #2
    use awk :
    awk 'BEGIN{P=1}{if(P==1||P==2){gsub(/^[@]/,">");print}; if(P==4)P=0; P++}' input.fastq > output.fasta

    Comment

    • nickloman
      Senior Member
      • Jul 2009
      • 355

      #3
      Ardmore, you are cluttering the forum with questions that can be resolved by looking at existing, easily located resources on the Internet. I've previously voiced my concerns in another thread that you are trying to use the forum to solve coursework problems which in my opinion is not a legitimate use for it.

      My feeling is there's only so much time and effort the community should be prepared to put into newbie questions like yours. I would suggest you enrol in a basic course on scripting and/or bioinformatics, read some basic bioinformatics tutorials, or find a mentor at your institution who can help you.

      If you feel I am being unfair, perhaps you can explain what your project is and why we should help you with basics like running perl scripts.

      Comment

      • ardmore
        Member
        • Jun 2011
        • 51

        #4
        I understand your concern. But I am not a student for my course worker. Actually my major is not bioinformatics but I am doing daily bioinformatics project. Maybe I selected a wrong career? I don't have a time to enroll a perl course because the work is due very soon and perl is rarely used.

        I hope this forum can have a subforum for newbie. Thanks for your time and advice. I will keep quite in this forum.

        Comment

        • swbarnes2
          Senior Member
          • May 2008
          • 910

          #5
          It's not that you are a newbie. This field is only a few years old, everyone here started as a newbie just a few years ago. But everyone else started by reading some documentation, so that they understood what the hell they were talking about. You don't even know what a fastq file is!

          By posting here, you are asking people to spend their own time to answer your questions. People are by and large willing to do that, but not when you have demonstrated that you haven't invested a lick of your own time to understand even the basics of the work you are trying to do.

          Comment

          • bioBob
            Member
            • Mar 2011
            • 72

            #6
            I like the awk script. I modified a perl snip I found to also convert '.' to 'N' I found in some Illumina fastqs:

            cat FILEIN | perl -e '$i=0;while(<>){if(/^\@/&&$i==0){s/^\@/\>/;print;}elsif($i==1){s/\./N/g;print;$i=-3}$i++;}' > FILEOUT

            Just change filein and fileout as appropriate.
            Good luck.

            Comment

            • mgogol
              Senior Member
              • Mar 2008
              • 197

              #7
              Also try the fastx toolkit.

              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, 10:52 AM
              0 responses
              9 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              19 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-13-2026, 09:56 AM
              0 responses
              16 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-09-2026, 11:14 AM
              0 responses
              27 views
              0 reactions
              Last Post SEQadmin2  
              Working...