Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • forget1997
    Junior Member
    • Jun 2011
    • 1

    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!
  • ECO
    --Site Admin--
    • Oct 2007
    • 1360

    #2
    Search please!

    Comment

    • lewewoo
      Member
      • Apr 2011
      • 60

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

      Comment

      • Simon Anders
        Senior Member
        • Feb 2010
        • 995

        #4
        why would you want to do this?

        Comment

        • cedance
          Senior Member
          • Feb 2011
          • 108

          #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

          • boetsie
            Senior Member
            • Feb 2010
            • 245

            #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

            • Apexy
              Member
              • Apr 2011
              • 62

              #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

              • 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
              • SEQadmin2
                Cancer Drug Resistance: The Lingering Barrier to Rising Survival
                by SEQadmin2



                Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

                There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
                07-08-2026, 05:17 AM
              • GATTACAT
                Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
                by GATTACAT
                Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
                07-01-2026, 11:43 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 07-09-2026, 10:04 AM
              0 responses
              24 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-08-2026, 10:08 AM
              0 responses
              15 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-07-2026, 11:05 AM
              0 responses
              33 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-02-2026, 11:08 AM
              0 responses
              31 views
              0 reactions
              Last Post SEQadmin2  
              Working...