Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • why doesn't this linux command work for me?

    Hi every one,
    I'd like merging the following two HTSeq-count outputs using the following command--- paste UHR1_htseq-count.out UHR2_htseq-count.out brain1_htseq-
    count.out brain2_htseq-count.out | awk -F "\t" '{print
    $1"\t"$2"\t"$4"\t"$6"\t"$8 }' > All_htseqCounts.txt


    head UHR1_htseq-count.out
    A1BG 67
    A1CF 31
    A2BP 3

    head UHR2_htseq-count.out
    A1BG 67
    A1CF 39
    A2BP 1
    -----
    I got the following output.

    A1BG 67 A1BG 67
    A1CF 31 A1CF 39
    A2BP 3 A2BP 1
    ----
    In fact I want to get the folloing one.

    A1BG 67 67
    A1CF 31 39
    A2BP 3 1

    Is there any one who know what is wrong with the command?

    Thanks a lot?

    Richard

  • #2
    paste file1 file2 | awk '{print $1" "$2" "$4}'

    Comment


    • #3
      Richard,
      I still got the same output---just merged the two files with ID of each kept.

      Comment


      • #4
        Perhaps tab isn't the default delimiter for paste on your system? Maybe then

        Code:
        paste -d "\t" file1 file2 | awk '{OFS="\t"; print $1,$2,$4}'
        Alternatively, perhaps the files aren't actually tab delimited to begin with (try running "cut -f 1" on one of them).

        Comment


        • #5
          Are you using bash?
          Run this command ...

          set | grep FS

          Also, look at the actual bytes ...
          od -x UHR1_htseq-count.out | head

          to see if that's a space or a tab.

          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...
            Yesterday, 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, 04-11-2024, 12:08 PM
          0 responses
          55 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          52 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          45 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          55 views
          0 likes
          Last Post seqadmin  
          Working...
          X