Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • weird fpkm value

    Hi, all:

    when I checked my paired-end RNAseq data, I saw some weird result.

    http://www.freeimagehosting.net/o9akt

    basically two genome features have same coordinate(as highlighted in red), however, their fpkm value is different. I wonder anyone have some ideas why this occur?

    By the way,
    I am using Tophat v2.0.4, Cufflinks v2.0.2 and cummeRbund v2.0.0.

    Thanks.

    Best,
    Liye

  • #2
    Hi,
    I suppose there could be a couple of reasons for this. It could be two different transcripts from the same gene. Or it could be antisense transcription.

    If you look at the column gene_short_name and look up those names you will indeed see that the second one is an antisense transcript. What I find a bit strange is when I look up DDX11L10 it is listed on chromosome 16, not chromosome 1. The gene on chromosome 1 at this locus is called DDX11L1.

    Comment


    • #3
      Hi, Blanco:

      Thanks for checking that out.
      Yes, the annotation file I used have some potential problem(DDX11L1 gene have one annotation at chr1 and chr16 as well). But I think I know what is the reason.

      I check the annotation for DDX11L1 of chr1, which spans 11869 to 13670.
      And RP11-34P13.3 spans 29554 to 30039.
      And Has-mir-1302-2 starts from 30366 to 30503.

      Therefore, I think the locus represents a transcript contig defined by cufflinks, which may include multiple transcripts. And each can have an unique ID. Therefore, both XLOC0001 and XLOC_00002 is within contig chr1:11868-31109.

      Best,
      Liye

      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
      17 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
      46 views
      0 likes
      Last Post seqadmin  
      Working...
      X