Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Minimum number of transcripts in cufflinks GTF

    Hi all,

    Would like to know if there is a minimum number of transcripts required in a GTF file in order for cufflinks to run properly?

    I've also tried this with cuffdiff:-
    1) full genome GTF
    2) take 10 transcripts out of the full GTF

    the FPKMs seem to pile on in the results from the smaller GTF file.

    Am I doing something wrong? The reason I'm doing this is for screening some potentially novel transcripts / locations in the genome, and would likely be working with a much smaller set of GTF entries.

    Advise is much welcomed!!!

  • #2
    FPKM is Fragments Per Kilobase per Million reads sequenced. Currently, Cufflinks calculates this "million reads sequenced" as "million reads mapped to the annotation", which is something we are looking at switching in the next version. To put the FPKMs on the same scale for the different runs, simply multiply the FPKMs by the "Total Map Mass" that Cufflinks prints to the screen. You can then divide by the number of reads from the full data and everything will be on the same scale.

    Comment


    • #3
      adarob, thank you for the clarification.

      does this mean the cuffdiff results have already taken this into account when computing fold change between 2 samples?

      because if each run has its own map mass and number of reads, then i would think that their fpkms will not be on the same scale.

      Comment


      • #4
        Since they both are forced to use the same GTF in cuffdiff, they will be on the same scale.

        Comment

        Latest Articles

        Collapse

        • seqadmin
          Recent Advances in Sequencing Analysis Tools
          by seqadmin


          The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
          Yesterday, 07:48 AM
        • seqadmin
          Essential Discoveries and Tools in Epitranscriptomics
          by seqadmin




          The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
          04-22-2024, 07:01 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, Yesterday, 07:17 AM
        0 responses
        12 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 05-02-2024, 08:06 AM
        0 responses
        19 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-30-2024, 12:17 PM
        0 responses
        20 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-29-2024, 10:49 AM
        0 responses
        29 views
        0 likes
        Last Post seqadmin  
        Working...
        X