Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • how to combine pair end data into one file

    Hi guys,
    I am a new comer for this forum.
    I just run pair end sequencing on Illumina hiseq 2000 and got two files. I was wondering how can I combine each read and output into a single file.
    Thanks!

  • #2
    Search please!

    Comment


    • #3
      Linux: cat or sth...
      Samtools, merge bam...

      Comment


      • #4
        why would you want to do this?

        Comment


        • #5
          I guess if you want to use hmmSplicer, then you'll have to merge the paired end reads. The software doesn't support separately yet.

          You could just use a basic unix command: cat pe1.fq pe2.fq > pe_merged.fq

          Comment


          • #6
            Some assemblers also require paired-end reads in one file, like Velvet and SSAKE. You can check their scripts to combine the paired-end reads into a single file with the scripts shufflesequences.pl and makePairedOutput2UNEQUALfiles.pl.

            Comment


            • #7
              Hi forget1997,
              In an attempt to answer your question, I would imagine your aim is to generate a file to be used by velveth. Should this be the case, there are two sample perl scripts "shuffleSequences_fasta.pl" (FASTA) & "shuffleSequences_fastq.pl" (FASTQ) that come with the velveth pakage. Provide them with your files and create a third file of shuffled sequences. If this is not what you want, try and explain a little more. Do you want to join Read1 & Read2 into one read? Do you want to combine both files (cedance & lewewoo suggest something to do this). A respond to Simon's question would surely bring you help.

              Comment

              Latest Articles

              Collapse

              • 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
              • seqadmin
                Strategies for Sequencing Challenging Samples
                by seqadmin


                Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
                03-22-2024, 06:39 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by seqadmin, 04-11-2024, 12:08 PM
              0 responses
              31 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 04-10-2024, 10:19 PM
              0 responses
              32 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 04-10-2024, 09:21 AM
              0 responses
              28 views
              0 likes
              Last Post seqadmin  
              Started by seqadmin, 04-04-2024, 09:00 AM
              0 responses
              53 views
              0 likes
              Last Post seqadmin  
              Working...
              X