[BioC] warnings or potential problems in limma procedure

Gordon K Smyth smyth at wehi.EDU.AU
Sat Apr 16 05:16:30 CEST 2011


Dear Ming,

You are getting a warning because your linear model is overparametrized. 
The AccNum factor already allows every patient to be different, so the 
extra variables Race and ER are redundant in a linear model sense.  You 
are including effects for every combination of Race and ER, that's four 
levels, so three extra degrees of freedom, so there must be three 
coefficients in your design matrix that are not estimable.  You can't 
estimate more coefficients for the patients than you have patients.  This 
really has to do a with linear models and model formula in R, rather than 
specifically with limma.

I expect that your results are nevertheless correct.  The linear model 
correctly removes the redundancies from the model and, fortunately for 
you, all the coefficients needed for your contrasts are retained.

Best wishes
Gordon


> Date: Wed, 13 Apr 2011 15:23:45 -0400
> From: "Yi, Ming (NIH/NCI) [C]" <yiming at mail.nih.gov>
> To: "bioconductor at r-project.org" <bioconductor at r-project.org>
> Subject: [BioC] warnings or potential problems in limma procedure
>
> Hi, Dear List:
>
> I am still looking for some explanation or diagnosis about the following 
> potential issue that I am not sure what I did is wrong or fine (I 
> apologize if my previous post is not quite clear to the list)
>
>
> I am using limma to do the paired test on the following setting, my tar 
> object looks like as below:
>
>> tar[1:5,]
>   AccNum Patient_Type_Comb Type RACE  ER
> 67 S10184    S10184_N_W_NEG    N    W NEG
> 66 S10184    S10184_T_W_NEG    T    W NEG
> 68 S10330    S10330_N_B_NEG    N    B NEG
> 69 S10330    S10330_T_B_NEG    T    B NEG
> 74 S10601    S10601_N_W_POS    N    W POS
>
> AccNum is the patient ID and the same patient have two types of samples: 
> "N" for normal, "T" for tumor,
>
> Two Races in the sample population: W for "White", B for "Black"
>
> ER is for ER status: NEG for negative, POS for positive
>
> Patient_Type_Comb column is for showing the sample phenotype in one 
> string
>
> The goal of the analysis is looking for the differential gene lists for 
> each of the contrasts including ER positive tumor vs ER positive normal 
> for matched same patient of only Black population (Africa America 
> population), ER negative tumor vs ER negative normal for matched same 
> patients of only White population (Caucasian population) etc as you can 
> see more details in my design and contrast matrix setting (the key is 
> need to consider the paired samples for the same patient with both tumor 
> and normal samples (normal is surrounding normal tissue of the tumor 
> tissue for the same patient), which is well controlled study.
>
>
> My data matrix (Partial, Array data) looks like the following:
>
>> mydata[1:5,1:4]
>        S10184_N_W_NEG S10184_T_W_NEG S10330_N_B_NEG S10330_T_B_NEG
> 7936596      10.079810      10.810695      10.733401      11.369506
> 8037331      10.076718      10.217359      10.921994      10.389894
> 8023672       8.503989       8.786565       8.936260       9.384205
> 8128282       5.423744       4.826185       5.872070       4.486140
> 8063634       5.909231       6.773356       6.653584       6.408861
>
> Here is how I set up my design and contrast matrix:
>
>> group1<-paste(tar$RACE,tar$Type,tar$ER, sep=".");
>> unique(group1)
> [1] "W.N.NEG" "W.T.NEG" "B.N.NEG" "B.T.NEG" "W.N.POS" "W.T.POS" "B.N.POS" "B.T.POS"
>> group<-factor(group1, levels=c(  "W.N.NEG","W.T.NEG", "B.N.NEG",
>> "B.T.NEG", "W.N.POS", "W.T.POS", "B.N.POS", "B.T.POS"))
>> Samples<-factor(tar$AccNum);
>
> design<-model.matrix(~-1+group+Samples);
>> colnames(design)<-sub("group","",colnames(design));
>> colnames(design)<-sub("Samples","",colnames(design));
>> con.matrix<-makeContrasts(T.POS_N.POS=B.T.POS+W.T.POS-B.N.POS-W.N.POS,
> + B.T.POS_B.N.POS=B.T.POS-B.N.POS,W.T.POS_W.N.POS=W.T.POS-W.N.POS,
> + T.NEG_N.NEG=B.T.NEG+W.T.NEG-B.N.NEG-W.N.NEG,
> + B.T.NEG_B.N.NEG=B.T.NEG-B.N.NEG, W.T.NEG_W.N.NEG=W.T.NEG-W.N.NEG,
> + levels=design)
>
>
> Here is the partial contrast matrix:
>> con.matrix[,]
>         Contrasts
> Levels    T.POS_N.POS B.T.POS_B.N.POS W.T.POS_W.N.POS T.NEG_N.NEG B.T.NEG_B.N.NEG W.T.NEG_W.N.NEG
>  W.N.NEG           0               0               0          -1               0              -1
>  W.T.NEG           0               0               0           1               0               1
>  B.N.NEG           0               0               0          -1              -1               0
>  B.T.NEG           0               0               0           1               1               0
>  W.N.POS          -1               0              -1           0               0               0
>  W.T.POS           1               0               1           0               0               0
>  B.N.POS          -1              -1               0           0               0               0
>  B.T.POS           1               1               0           0               0               0
>  S10330            0               0               0           0               0               0
>  S10601            0               0               0           0               0               0
>  S10618            0               0               0           0               0               0
>  S10929            0               0               0           0               0               0
>  S10940            0               0               0           0               0               0
>
>
> However, when I tried to fit the data into the limma model, I run into the following warnings, which is what I am trying asking about:
>
>> lmFit(mydata,design)->fit1;
> Coefficients not estimable: S14697 S14730 S14810 Warning message:
> Partial NA coefficients for 26804 probe(s)
>
> This warning seems not bothering the subsequent steps as shown below, but I am not sure why I get warning here, could the list provide some insights or clues for me? that would be highly appreciated!
>
>> contrasts.fit(fit1, con.matrix)->fit2
>> eBayes(fit2)->fit3
>> allContrast<-colnames(fit3);
>> allContrast
> [1] "T.POS_N.POS"     "B.T.POS_B.N.POS" "W.T.POS_W.N.POS" "T.NEG_N.NEG"     "B.T.NEG_B.N.NEG" "W.T.NEG_W.N.NEG"
>
> I also did check specifically for the samples listed in the warning message
>
>> tar[tar$AccNum %in% c("S14697", "S14730", "S14810"),]
>   AccNum Patient_Type_Comb Type RACE  ER
> 57 S14697    S14697_N_W_POS    N    W POS
> 58 S14697    S14697_T_W_POS    T    W POS
> 55 S14730    S14730_N_B_NEG    N    B NEG
> 56 S14730    S14730_T_B_NEG    T    B NEG
> 59 S14810    S14810_N_B_POS    N    B POS
> 60 S14810    S14810_T_B_POS    T    B POS
>
> They appear to be common, which of all have paired samples (T vs N) and some of which are white/black and some are ER Negative and positive, seems not fall into any of the special category of the phenotype.
>
> I also check specifically for their data as below:
>
>> mydata[1:5,c("S14697_N_W_POS", "S14697_T_W_POS", "S14730_N_B_NEG",
>> "S14730_T_B_NEG", "S14810_N_B_POS", "S14810_T_B_POS")]
>        S14697_N_W_POS S14697_T_W_POS S14730_N_B_NEG S14730_T_B_NEG S14810_N_B_POS S14810_T_B_POS
> 7936596      11.024855      10.954703      10.832579      10.917364      10.631019      10.842098
> 8037331       9.807050      10.366058      10.285187       9.955208      10.410920      10.620751
> 8023672       8.734080       8.359230       8.559288       8.245623       8.613978       8.614790
> 8128282       5.489218       5.703427       5.026220       4.738774       5.362589       5.193500
> 8063634       6.562237       6.784427       6.632752       6.757525       6.887120       7.095357
>
>
> Which also look normal to me.
>
> Thanks a lot in advance for your advice and suggestion!
>
> Best
>
> Ming
>
> Ming Yi, Ph.D.
> Information System Program
> SAIC-Frederick, Inc.
> National Cancer Institute at Frederick
> Post Office Box B,
> Frederick, MD 21702

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