Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Paired-end Bam from single-end aligned sam

    Hi,
    I have 2 sam(reverse and farward) files generated by bowtie.
    I would like to generate a paired-end bam file from the 2 sam files.
    using samtools merge -nr generate only a file with the concatenation of the singles reads from bothb file but do not do the pairing
    tried also samtools fixmate but it's not working.
    I've looked at the spec for SAM format, in 1.4.4. Storing paired-end reads the following is stated : "A tool is also provided to reconstruct mating information from BAM, although this is done at the cost of intensive computation and large disk space."
    Is there any tool that allow to do the pairing of single reads based on the read ID ?
    Thanks in advance for your help,
    Regards,
    Ramzi
    Last edited by ramouz87; 07-20-2010, 05:20 AM.
    Research Scientist - Bioinformatics
    Sidra Medical and Research Center

  • #2
    Hi everyone!
    Did you manage to get an answer for your question dear ramouz87?
    I have a similar questions except that I have two .bam files that include the pairs that are mapped, separately. I want to associate the pairs and have the results as a single .bam file.

    Does anyone know how that is possible?

    Comment


    • #3
      I just came to this site to ask the same question - I have two sam files from Bowtie that come from paired end reads and I want to create one sam or bam file that incorporates the paired end information.

      Eric

      Comment


      • #4
        Please redo the alignment with a mapper supporting proper paired-end mapping. Merging single-end alignment afterwards always gives you worse results.

        Comment


        • #5
          @ efoss, oghabian, ramouz87

          I don't think there's any reasonable way to get from one to the other. The alignments you got by treating the reads as singles are not the same as what you'll get if you align them as paired. You can either redo the alignment as paired (the best solution) or forge ahead with what you've got treating the reads as single end.

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Recent Advances in Sequencing Analysis Tools
            by seqadmin


            The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
            05-06-2024, 07:48 AM
          • 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

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, Yesterday, 06:57 AM
          0 responses
          12 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 05-06-2024, 07:17 AM
          0 responses
          16 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 05-02-2024, 08:06 AM
          0 responses
          19 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-30-2024, 12:17 PM
          0 responses
          24 views
          0 likes
          Last Post seqadmin  
          Working...
          X