Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Cufflinks FPKM inconsistent with reads in IGV

    I have 6 samples the FPKM is as following:
    0 0 0.23 0.15 0.56 0.3

    however, when I used IGV to double checked the reads mapped, there are a lot of reads and the amounts mapped in the loci are pretty same; the total reads are not very different.

    Any suggestions?

  • #2
    All those FPKMs are very low. Do you have any better examples ? I've seen this before in my data.

    The FPKM estimates make no sense. For one, the second transcript from the top has no reads spanning the last intron. I scrolled all the way to the bottom. But it has a FPKM of 53.

    I'm also not sure why the bottom-most transcript has a FPKM of 272. There are very few reads in the exonic part that is unique to it.

    In summary, you don't want to trust Cufflinks estimates. They make no sense. Have you tried NEUMA instead ?

    Comment


    • #3
      I found NEUMA work great and the results do make sense at many genes mannually checked.

      Originally posted by Dario1984 View Post
      All those FPKMs are very low. Do you have any better examples ? I've seen this before in my data.

      The FPKM estimates make no sense. For one, the second transcript from the top has no reads spanning the last intron. I scrolled all the way to the bottom. But it has a FPKM of 53.

      I'm also not sure why the bottom-most transcript has a FPKM of 272. There are very few reads in the exonic part that is unique to it.

      In summary, you don't want to trust Cufflinks estimates. They make no sense. Have you tried NEUMA instead ?

      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
      30 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      32 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      28 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      53 views
      0 likes
      Last Post seqadmin  
      Working...
      X