Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Determine paired end overlapping

    I have a paired end Illumina exome data set that might have overlapped at the ends. My fragment size has 105 bp. I aligned my samples with bwa and generated my bam files with samtools.
    My question is:

    Is there any way to determine how many reads overlapped?

    How can I determine the distance between the paired ends (in case they didn´t overlap) or how much they overlapped?

    If this percentage is high, I am thinking about reanalyzing my data generating fragments of 75 or 50bp. Do you think that’s correct? Which percentage could be the cut-off to consider it high?

    Thanks
    Last edited by chariko; 04-13-2011, 08:29 AM.

  • #2
    in the SAM/BAM the TLEN column will tell you the template length. if it is smaller than 2*105bp you have overlapping ends (if there are no indels).

    try this to see the template length distribution of the first million reads: samtools view PEalignment.bam | head -n 1000000 | cut -f 9 | sort -n | uniq -c

    why would you want to generate fragments?

    Comment


    • #3
      Originally posted by volks View Post
      in the SAM/BAM the TLEN column will tell you the template length. if it is smaller than 2*105bp you have overlapping ends (if there are no indels).

      try this to see the template length distribution of the first million reads: samtools view PEalignment.bam | head -n 1000000 | cut -f 9 | sort -n | uniq -c

      why would you want to generate fragments?
      Thanks for your answer, with the TLEN column I could manage it.

      Regarding your question, the problem of having too much overlap is that I will miss the advantages of an paired end experiment that is detection of structural variants in the genome between the pairs for example. So if I generated 75 bases fragments I would have less overlapping. I know it's better if you work with longer reads but I thought this could be a solution. Also I think there are softwares that can get this info even if pairs overlap but I don´t know yet which of them. Do you have an idea?
      Last edited by chariko; 04-28-2011, 11:57 PM.

      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
      18 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      22 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      16 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      47 views
      0 likes
      Last Post seqadmin  
      Working...
      X