Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • orthodoc
    Junior Member
    • Oct 2013
    • 2

    cummeRbund scatterplot labels

    Hi Everyone,

    Disclaimer: I am very new to next gen sequencing / the Tuxedo suite of tools so please excuse gross incompetence!

    I am using cummeRbund to visualize the results of my Cuffdiff run and while it is very impressive, I have a few questions about the figures it generates. I have 3 replicates of 5 conditions, each condition was compared head-to-head in 4 individual cuffdiff runs (this was done by our university's bioinformatics core).

    I would like to take a selection of the most significant deferentially expressed genes and present it on a scatterplot. My workflow to accomplish this has been to look through gene_exp.diff in Excel, manually filter and sort as necessary, then pick my genes of interest and go back to R to create a gene set with these id's, then plot away. It works fine up to this point.

    I can create the scatterplot, but it is of limited utility unlabeled. I would like to label each of the points (I'm only using about 20 genes in each set) with what gene it represents. Is this possible?

    This would make my analysis much much easier than manually looking through the gene_exp.diff tables.

    Please let me know if anyone has any suggestions or if I'm approaching this in the wrong way.

    Thanks!

    -orthodoc
  • cbaudo
    Member
    • Jan 2013
    • 21

    #2
    Hello orthodoc,

    I was wondering if you found a solution to this problem.

    Thank you,
    cbaudo

    Comment

    • sindrle
      Senior Member
      • Aug 2013
      • 266

      #3
      I recommend the CummeRbund manuals section about "Creating Gene Set".

      You really don't need Excel for anything.

      Going this route you may then use ggplot2 commands on your gene set and alter your plot as you like, works like a charm.

      Comment

      • cbaudo
        Member
        • Jan 2013
        • 21

        #4
        Thanks sindrle,
        I've successfully imported by data into R and labeled the points on the scatterplot with gene IDs, but I am encountering another issue. I would like to modify the axis intervals in the same way cummeRbund does. Currently, a majority of my data points are clustered together with low FPKM values, but a few genes have large FPKM values which skew the graph to have larger axis. All of the points are then smooshed together.

        Do you know of an R function I can use or of a work around for this? Also, do you know if cummeRbund log transforms the data prior to plotting?

        cheers,
        cbaudo

        Comment

        • sindrle
          Senior Member
          • Aug 2013
          • 266

          #5
          I would read about ggplot2, its this package used by cummerbund. I can handle everything like this.

          see the help() function for the plot, it should be an option called log = TRUE, or something like that.

          Good luck!

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Nine Things a Sample Prep Scientist Thinks About Before Sequencing
            by SEQadmin2


            I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

            Here are nine questions we think about, in roughly the order they matter, before...
            06-18-2026, 07:11 AM
          • SEQadmin2
            From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
            by SEQadmin2


            Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


            The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
            ...
            06-02-2026, 10:05 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 06-17-2026, 06:09 AM
          0 responses
          36 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-09-2026, 11:58 AM
          0 responses
          99 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-05-2026, 10:09 AM
          0 responses
          120 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 06-04-2026, 08:59 AM
          0 responses
          113 views
          0 reactions
          Last Post SEQadmin2  
          Working...