Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • DESeq2 model design: dose and time effect

    i have three samples each with 3 biological replicates i.e. one control and other at dose 12ug/ml and 25ug/ml at 24hr

    > library('DESeq2')

    > directory<-"./data"

    > sampleFiles <- grep("Htseq",list.files(directory),value=TRUE)

    > sampleCondition<-c("treated","treated","treated","treated","treated","treated","untreated","untreated","untreated")

    > sampleGroup <-c ("A","A","A","B","B","B","C","C","C")

    > sampleTable<-data.frame(sampleName=sampleFiles, fileName=sampleFiles, condition=sampleCondition, group=sampleGroup)

    > sampleTable

    sampleName fileName condition group
    1 24h_12ug_1.count 24h_12ug_1.count treated A
    2 24h_12ug_2.count 24h_12ug_2.count treated A
    3 24h_12ug_3.count 24h_12ug_3.count treated A
    4 24h_25ug_1.count 24h_25ug_1.count treated B
    5 24h_25ug_2.count 24h_25ug_2.count treated B
    6 24h_25ug_3.count 24h_25ug_3.count treated B
    7 24h_ctrl_1.count 24h_ctrl_1.count untreated C
    8 24h_ctrl_2.count 24h_ctrl_2.count untreated C
    9 24h_ctrl_3.count 24h_ctrl_3.count untreated C

    what should be good design if i want to see the differential expressed genes between treated vs untreated as well between different groups ?

    ddsHTSeq<-DESeqDataSetFromHTSeqCount(sampleTable=sampleTable, directory=directory, design=~group)
    OR
    ddsHTSeq<-DESeqDataSetFromHTSeqCount(sampleTable=sampleTable, directory=directory, design=~condition)

    what will be the difference between the two designs?


    I tried the following design but it gave me error

    ddsHTSeq<-DESeqDataSetFromHTSeqCount(sampleTable=sampleTable, directory=directory, design=~group + condition + condition:group)

    Error in DESeqDataSet(se, design = design, ignoreRank) :
    the model matrix is not full rank, so the model cannot be fit as specified.
    one or more variables or interaction terms in the design formula
    are linear combinations of the others and must be removed



    how will the design will change if i add three samples each with 3 biological replicates i.e. one control and other at dose 12ug/ml and 25ug/ml at 6hr
    Last edited by imsharmanitin; 08-11-2015, 08:05 AM.

  • #2
    Refer to https://www.biostars.org/p/154250/ for answer.
    Last edited by GenoMax; 08-12-2015, 07:01 AM. Reason: Clarified that question has been answered

    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
    18 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
    17 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    49 views
    0 likes
    Last Post seqadmin  
    Working...
    X