Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • cut reads befor N

    Hi,

    I have reads with final Ns. Let's say, how can I get from this :

    >R1
    GGGGGGGTTTTTTTTTTTTTTTNT
    >R2
    GGGGGGGGGGTTTTTTTTTTNTTNT

    to this (basically I want to cut the reads before the first N):

    >R1
    GGGGGGGTTTTTTTTTTTTTTT
    >R2
    GGGGGGGGGGTTTTTTTTTT

  • #2
    You could try:

    sed 's/^\([ATGC]*\)N\([ATGCN]*\)/\1/g' YOURFILE > NEWFILE

    at least if you have a *nix operating system.

    Comment


    • #3
      Thanks, that works only for the first hit of my fasta file. How can I do that for all the sequences?

      Comment


      • #4
        This command is cute and simple.
        If there any Ns in the sequence identifiers of your FASTA file, they will also be trimmed off, however.

        Code:
        cut -d N -f 1 test.fa
        Code:
        [blancha@lg-1r17-n04 ~]$ more test.fa 
        >R1
        GGGGGGGTTTTTTTTTTTTTTTNT
        >R2
        GGGGGGGGGGTTTTTTTTTTNTTNT
        [blancha@lg-1r17-n04 ~]$ cut -d N -f 1 test.fa 
        >R1
        GGGGGGGTTTTTTTTTTTTTTT
        >R2
        GGGGGGGGGGTTTTTTTTTT
        Last edited by blancha; 10-19-2015, 06:48 AM.

        Comment


        • #5
          Originally posted by Pol8 View Post
          Thanks, that works only for the first hit of my fasta file. How can I do that for all the sequences?
          Do you have a dos/OS X formatted file? You may need to pass it through dos2unix/mac2unix utility before using @dschika's code.

          @dschika's code works for me.

          Comment


          • #6
            Is GenoMax's assumption right? That may cause problems...

            Just in case:
            Code:
            sed 's/^\([ATGC]*\)N\([ATGCN]*\)/\1/g' test.fa
            >R1
            GGGGGGGTTTTTTTTTTTTTTT
            >R2
            GGGGGGGGGGTTTTTTTTTT
            ... and this solution does not alter the sequence identifiers
            Last edited by dschika; 10-19-2015, 07:06 AM.

            Comment


            • #7
              I hadn't realised the sed command worked.
              @dscika, better than my cut example too.

              I'm posting my awk command anyway, since I spent a bit of time researching it.
              It will not trim the N in the sequence identifier, like my simpler cut command.

              Code:
              awk -F "N" '{if (NR % 2==0) {print $1} else {print}}' test2.fa
              Code:
              [blancha@lg-1r17-n04 ~]$ more test2.fa 
              >R1 N in the sequence identifier.
              GGGGGGGTTTTTTTTTTTTTTTNT
              >R2
              GGGGGGGGGGTTTTTTTTTTNTTNT
              [blancha@lg-1r17-n04 ~]$ awk -F "N" '{if (NR % 2==0) {print $1} else {print}}' test2.fa 
              >R1 N in the sequence identifier.
              GGGGGGGTTTTTTTTTTTTTTT
              >R2
              GGGGGGGGGGTTTTTTTTTT

              Comment


              • #8
                Also quite nice!

                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...
                  04-22-2024, 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, Today, 11:49 AM
                0 responses
                8 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, Yesterday, 08:47 AM
                0 responses
                16 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 04-11-2024, 12:08 PM
                0 responses
                61 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 04-10-2024, 10:19 PM
                0 responses
                60 views
                0 likes
                Last Post seqadmin  
                Working...
                X