Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts

  • zsanli
    replied
    how to delete most 0 values

    Originally posted by Greg Deakin View Post
    I had the same issue as well - it was caused by some extremely low dispersion (and count) values. Some were of the order of 10e-308, which is lower than the minimum floating point value supported by R (on my architecture anyway). I set these to 0 and the plot then worked.

    I need to read up a bit more about cuffdiff - obviously it normalises the count values, but I can't see why any should be much less than 1.

    Greg
    I have same trouble when I draw disperse graph. Do you know how to code to delete most small values and small counts e.g. 2e-168

    Leave a comment:


  • Greg Deakin
    replied
    I had the same issue as well - it was caused by some extremely low dispersion (and count) values. Some were of the order of 10e-308, which is lower than the minimum floating point value supported by R (on my architecture anyway). I set these to 0 and the plot then worked.

    I need to read up a bit more about cuffdiff - obviously it normalises the count values, but I can't see why any should be much less than 1.

    Greg

    Leave a comment:


  • chodar
    replied
    Same issue for me. In other forum I read that "#" character in gtf file have to be removed. In my case I dont have # but still have the error.

    Thanks.
    Last edited by chodar; 03-09-2015, 09:44 AM.

    Leave a comment:


  • jake13
    replied
    I'm having the same issue if anyone has a solution?

    Leave a comment:


  • frymor
    started a topic error in cummeRbund dispersionPlot

    error in cummeRbund dispersionPlot

    Hi,

    I am trying to run cummeRbund with the cuffdiff results.
    these is my workflow:

    Code:
    library(cummeRbund)
    
    setwd("cummeRbund/")
    
    cuff <- readCufflinks(dir=cuffFile_dir, gtfFile="merged.gtf", genome="dm3" , rebuild=TRUE)
    everything seems to run good. all tables are ok, but I am getting these warnings:
    Code:
    Warning messages:
    
    1: attributes are not identical across measure variables; they will be dropped 
    ...
    8: attributes are not identical across measure variables; they will be dropped
    I have read here, that these messages can be ignored, so I am not sure they're connected to my problem.

    I am than trying to execute the DispersionPlot commend. But this gives me an error:

    Code:
    > disp<-dispersionPlot(genes(cuff))
    > disp
    [B]Error in seq.default(min, max, by = by) : 
      'from' cannot be NA, NaN or infinite[/B]

    Does anyone have an idea why I get this error?
    How can I prevent this from happening?

    thanks

    Assa

    #####
    > sessionInfo()
    R version 3.1.1 (2014-07-10)
    Platform: x86_64-apple-darwin13.1.0 (64-bit)

    locale:
    [1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

    attached base packages:
    [1] grid stats4 parallel stats graphics grDevices utils
    [8] datasets methods base

    other attached packages:
    [1] mgcv_1.8-3 nlme_3.1-118 cummeRbund_2.8.2
    [4] Gviz_1.10.2 rtracklayer_1.26.1 GenomicRanges_1.18.1
    [7] GenomeInfoDb_1.2.2 IRanges_2.0.0 S4Vectors_0.4.0
    [10] fastcluster_1.1.13 reshape2_1.4 ggplot2_1.0.0
    [13] RSQLite_1.0.0 DBI_0.3.1 BiocGenerics_0.12.0

    loaded via a namespace (and not attached):
    [1] acepack_1.3-3.3 AnnotationDbi_1.28.1 base64enc_0.1-2
    [4] BatchJobs_1.5 BBmisc_1.8 Biobase_2.26.0
    [7] BiocParallel_1.0.0 biomaRt_2.22.0 Biostrings_2.34.0
    [10] biovizBase_1.14.0 bitops_1.0-6 brew_1.0-6
    [13] BSgenome_1.34.0 checkmate_1.5.0 cluster_1.15.3
    [16] codetools_0.2-9 colorspace_1.2-4 dichromat_2.0-0
    [19] digest_0.6.4 fail_1.2 foreach_1.4.2
    [22] foreign_0.8-61 Formula_1.1-2 GenomicAlignments_1.2.1
    [25] GenomicFeatures_1.18.2 gtable_0.1.2 Hmisc_3.14-5
    [28] iterators_1.0.7 labeling_0.3 lattice_0.20-29
    [31] latticeExtra_0.6-26 MASS_7.3-35 Matrix_1.1-4
    [34] matrixStats_0.10.3 munsell_0.4.2 nnet_7.3-8
    [37] plyr_1.8.1 proto_0.3-10 R.methodsS3_1.6.1
    [40] RColorBrewer_1.0-5 Rcpp_0.11.3 RCurl_1.95-4.3
    [43] rpart_4.1-8 Rsamtools_1.18.1 scales_0.2.4
    [46] sendmailR_1.2-1 splines_3.1.1 stringr_0.6.2
    [49] survival_2.37-7 tools_3.1.1 VariantAnnotation_1.12.3
    [52] XML_3.98-1.1 XVector_0.6.0 zlibbioc_1.12.0
    Last edited by frymor; 11-10-2014, 05:22 AM.

Latest Articles

Collapse

  • SEQadmin2
    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
    by SEQadmin2



    Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

    Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
    ...
    10-14-2026, 09:55 AM
  • SEQadmin2
    New Genomics Technologies Take Aim at Long-Standing Limits
    by SEQadmin2


    Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

    We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
    ...
    09-28-2026, 10:25 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Yesterday, 11:13 AM
0 responses
19 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, Yesterday, 10:48 AM
0 responses
18 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
36 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
42 views
0 reactions
Last Post SEQadmin2  
Working...