Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • hujiacun
    Member
    • Mar 2015
    • 17

    #1

    how to sort out mate no mapped reads

    Hi,
    I am now doing some analysis about chromosome structure Viaration. Please help me about following questions.
    1. Is there any method to sort out reads which mate is no mapped by IGV dispaly. I have dreamed that pair end all mapped reads are not displayed, so I could see what I wanted.
    2.If IGV can't do it, is there any methods to sort out single mapped reads from SAM or BAM files. As to the sinle mapped reads,some single mapped reads may scatter around the genome, some may concentrated on one loci. the later situation may reflect a real SV. So is there any method to find concentrated single mapped reads.
  • diego diaz
    Member
    • Oct 2013
    • 62

    #2
    with samtools you can perform the analysis :

    if you have paired-end reads : "samtools view -f 8 -F 4 file.bam" will give you mapped reads with unmapped mate.

    if you have unpaired + paired reads: "samtools view -F1 file.bam" will give you unpaired mapped reads

    reads concentration, as you say, means deep coverage. To check the coverage along the genome you could use genomeCoverageBed:

    genomeCoverageBed -ibam sortedBamFile.bam -g genome.txt > coverage.txt

    Paired reads with a bad insert size or mis-oriented also could be evidence of structural variation.

    please see this image:



    When you map your reads to some reference you will see similar patterns in regions with structural variation.

    Comment

    • hujiacun
      Member
      • Mar 2015
      • 17

      #3
      fastq indicate "table not found"

      Who can tell me why err like this after I enter "fastq-dump -X 5 -Z SRR616966"
      2015-04-13T15:23:47 fastq-dump.2.1.7 err: table not found while opening manager within database module - failed to open 'SRR616966'

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
        by SEQadmin2




        NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
        Today, 06:46 AM
      • SEQadmin2
        Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
        by SEQadmin2



        Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

        Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
        ...
        10-14-2026, 09:55 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 10-28-2026, 09:57 AM
      0 responses
      24 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-28-2026, 09:51 AM
      0 responses
      15 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 11:13 AM
      0 responses
      68 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 10:48 AM
      0 responses
      48 views
      0 reactions
      Last Post SEQadmin2  
      Working...