Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Pol8
    Member
    • Aug 2014
    • 33

    #1

    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
  • dschika
    Member
    • Mar 2010
    • 56

    #2
    You could try:

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

    at least if you have a *nix operating system.

    Comment

    • Pol8
      Member
      • Aug 2014
      • 33

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

      Comment

      • blancha
        Senior Member
        • May 2013
        • 367

        #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

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #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

          • dschika
            Member
            • Mar 2010
            • 56

            #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

            • blancha
              Senior Member
              • May 2013
              • 367

              #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

              • dschika
                Member
                • Mar 2010
                • 56

                #8
                Also quite nice!

                Comment

                Latest Articles

                Collapse

                • SEQadmin2
                  Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                  by SEQadmin2



                  CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                  Despite this, “CRISPR helped turn genome editing from a specialized technique into
                  ...
                  07-31-2026, 11:01 AM
                • SEQadmin2
                  Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                  by SEQadmin2


                  Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                  The systematic characterization of the human proteome has
                  ...
                  07-20-2026, 11:48 AM
                • SEQadmin2
                  Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
                  by SEQadmin2



                  Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
                  ...
                  07-09-2026, 11:10 AM

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by SEQadmin2, 07-31-2026, 02:55 AM
                0 responses
                18 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-24-2026, 12:17 PM
                0 responses
                16 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-23-2026, 11:41 AM
                0 responses
                16 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-20-2026, 11:10 AM
                0 responses
                26 views
                0 reactions
                Last Post SEQadmin2  
                Working...