Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Reads mapped on junctions

    Hello everybody,


    I work with Tophat to align paired-end reads.

    By reading one of the log-files that it produces: reports.log,
    I can know the number of the Loaded junctions and the Found junctions.
    Does anyone know how can I count the reads mapping on the Found Junctions?


    Thanks,
    nike00

  • #2
    There should be a file "junctions.bed" that gives you a detailed information regarding the junction coordinates and the number of reads.

    Alternatively you could do it yourself from the SAM/BAM file, if you go through the SAM format manual. If you would like to do it by yourself, if necessary, I'll explain in detail.

    Comment


    • #3
      Dear cedance,

      thanks a lot for your reply and suggestions.
      I have checked the file "junctions.bed" and, as well as I have understood, there is a column (the fifth one) reporting a score. The score is the number of alignments spanning the junction (from the Tophat Manual).
      It exactly is the number of pairs (of reads) spanning the junctions, isn't it? or the total number of the reads?

      PS: For sure I'm going to explore the SAM file by myself, so I will post again if necessary.

      Thanks very much,
      nike00

      Comment


      • #4
        nike00, I am glad I could be of help.
        I think its the total number of reads that span the junction. The other pair of the read (that is mapped across this junction) need not span the same junction, as it depends on the fragment length (or inner distance as Tophat says it) you chose (after adapter + optionally barcode ligation).

        Therefore, the number given by junctions.bed is the number of reads spanning the junction and not necessarily its pairs.

        Paired end reads, imho, are used for better mapping efficiency. You could find out the number of reads where both pairs map to the same junction, but I don't see why or what is the use.

        I'm in bit of a hurry, if what I wrote is more confusing, please reply back and I'll try to explain better what I meant/think.

        Comment

        Latest Articles

        Collapse

        • seqadmin
          Best Practices for Single-Cell Sequencing Analysis
          by seqadmin



          While isolating and preparing single cells for sequencing was historically the bottleneck, recent technological advancements have shifted the challenge to data analysis. This highlights the rapidly evolving nature of single-cell sequencing. The inherent complexity of single-cell analysis has intensified with the surge in data volume and the incorporation of diverse and more complex datasets. This article explores the challenges in analysis, examines common pitfalls, offers...
          06-06-2024, 07:15 AM
        • seqadmin
          Latest Developments in Precision Medicine
          by seqadmin



          Technological advances have led to drastic improvements in the field of precision medicine, enabling more personalized approaches to treatment. This article explores four leading groups that are overcoming many of the challenges of genomic profiling and precision medicine through their innovative platforms and technologies.

          Somatic Genomics
          “We have such a tremendous amount of genetic diversity that exists within each of us, and not just between us as individuals,”...
          05-24-2024, 01:16 PM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, 06-07-2024, 06:58 AM
        0 responses
        13 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 06-06-2024, 08:18 AM
        0 responses
        23 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 06-06-2024, 08:04 AM
        0 responses
        20 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 06-03-2024, 06:55 AM
        0 responses
        14 views
        0 likes
        Last Post seqadmin  
        Working...
        X