| Title: | Phenotype prediction using microarray data: approach of the best overall team in the IMPROVER Diagnostic Signature Challenge |
|---|---|
| Description: | This package implements the classification pipeline of the best overall team (Team221) in the IMPROVER Diagnostic Signature Challenge. Additional functionality is added to compare 27 combinations of data preprocessing, feature selection and classifier types. |
| Authors: | Adi Laurentiu Tarca <[email protected]> |
| Maintainer: | Adi Laurentiu Tarca <[email protected]> |
| License: | GPL-2 |
| Version: | 1.45.0 |
| Built: | 2024-12-20 02:44:00 UTC |
| Source: | https://github.com/bioc/maPredictDSC |
This function simply adds the posterior probabilities for a given class and sample from several models, and scales the resulting sums so that the sum over the classes is 1.0.
aggregateDSC(modlist)aggregateDSC(modlist)
modlist |
An object returned by predictDSC. |
See cited documents for more details.
A a data frame with the predicted class membership belief value (posterior probability) for each sample (row) and each class (column).
Adi Laurentiu Tarca <[email protected]>
Adi L. Tarca, Mario Lauria, Michael Unger, Erhan Bilal, Stephanie Boue, Kushal Kumar Dey,
Julia Hoeng, Heinz Koeppl, Florian Martin, Pablo Meyer, Preetam Nandy, Raquel Norel,
Manuel Peitsch, Jeremy J Rice, Roberto Romero, Gustavo Stolovitzky, Marja Talikka,
Yang Xiang, Christoph Zechner, and IMPROVER DSC Collaborators,
Strengths and limitations of microarray-based phenotype prediction: Lessons learned
from the IMPROVER Diagnostic Signature Challenge. Bioinformatics, submitted 2013.
Tarca AL, Than NG, Romero R, Methodological Approach from the Best Overall
Team in the IMPROVER Diagnostic Signature Challenge, Systems Biomedicine, submitted, 2013.
#see function predictDSC for example#see function predictDSC for example
This function implements the three metrics used in the IMPROVER Diagnostic Signature Challenge.
perfDSC(pred,gs)perfDSC(pred,gs)
pred |
A belief matrix, with rows coresponding to samples and columns to classes. The values are between 0 and 1 and sum on each row is 1. It needs to have row names. The belief values are the result of a prediction made by a model. |
gs |
A matrix, with rows coresponding to samples and columns to classes that give the true (gold standard) class membership of samples. |
See cited documents for more details.
A named vector that includes the BCM, CCEM, AUPR_avg and Accuracy.
Adi Laurentiu Tarca <[email protected]>
Adi L. Tarca, Mario Lauria, Michael Unger, Erhan Bilal, Stephanie Boue, Kushal Kumar Dey,
Julia Hoeng, Heinz Koeppl, Florian Martin, Pablo Meyer, Preetam Nandy, Raquel Norel,
Manuel Peitsch, Jeremy J Rice, Roberto Romero, Gustavo Stolovitzky, Marja Talikka,
Yang Xiang, Christoph Zechner, and IMPROVER DSC Collaborators,
Strengths and limitations of microarray-based phenotype prediction: Lessons learned
from the IMPROVER Diagnostic Signature Challenge. Bioinformatics, submitted 2013.
#asume a 3 class classification problem; gs is the gold standard and pred are predictions gs=cbind(A=c(1,1,1,1,0,0,0,0,0,0,0,0),B=c(0,0,0,0,1,1,1,1,0,0,0,0),C=c(0,0,0,0,0,0,0,0,1,1,1,1)) rownames(gs)<-paste("sample",1:12,sep="") pred=cbind(A=c(0.6,0.9,1,0.3,0,0,0,0,0,0,0,0),B=c(0.4,0.1,0,0.7,1,1,0.7,1,0,0,0,0),C=c(0,0,0,0,0,0,0.3,0,1,1,1,1)) rownames(pred)<-paste("sample",1:12,sep="") #male sure the sum per row is 1 is both gs and pred apply(gs,1,sum) apply(pred,1,sum) #compute perfromance perfDSC(pred,gs)#asume a 3 class classification problem; gs is the gold standard and pred are predictions gs=cbind(A=c(1,1,1,1,0,0,0,0,0,0,0,0),B=c(0,0,0,0,1,1,1,1,0,0,0,0),C=c(0,0,0,0,0,0,0,0,1,1,1,1)) rownames(gs)<-paste("sample",1:12,sep="") pred=cbind(A=c(0.6,0.9,1,0.3,0,0,0,0,0,0,0,0),B=c(0.4,0.1,0,0.7,1,1,0.7,1,0,0,0,0),C=c(0,0,0,0,0,0,0.3,0,1,1,1,1)) rownames(pred)<-paste("sample",1:12,sep="") #male sure the sum per row is 1 is both gs and pred apply(gs,1,sum) apply(pred,1,sum) #compute perfromance perfDSC(pred,gs)
This function implements the classification pipeline of the best overall team (Team221) in the IMPROVER Diagnostic Signature Challenge. The function ofers also eploring other combinations of data preprocessing, feature selection and classifier types.
predictDSC(ano,celfile.path,annotation,preprocs=c("rma","gcrma","mas5"), filters=c("mttest","ttest","wilcox"),classifiers=c("LDA","kNN","svm"),FCT=1.0, CVP=4,NF=10,by=ifelse(NF>10,2,1), NR=5)predictDSC(ano,celfile.path,annotation,preprocs=c("rma","gcrma","mas5"), filters=c("mttest","ttest","wilcox"),classifiers=c("LDA","kNN","svm"),FCT=1.0, CVP=4,NF=10,by=ifelse(NF>10,2,1), NR=5)
ano |
A data frame with two columns: |
celfile.path |
The location of the directory where the .cel files are located. |
annotation |
The names of a package that can be used to map the probesets to the ENTREZ
gene IDS in order to deal with duplicate probesets pre gene. E.g. |
preprocs |
A character vector giving the names of the normalization methods to try. Supported options are "rma","gcrma","mas5" |
filters |
A character vector giving the names of the methods to use to rank features. Supported options are "mttest" for moderated t-test using limma package,"ttest" for regular t-test, and "wilcox" for wilcoxon test. |
classifiers |
A character vector giving the names of the classifier types to use for learning the relation between expression levels and phenotype. Supported options are "LDA","kNN","svm". |
FCT |
A numeric value giving the fold change threshokd to be used to filter out non-relevant
features. Note, setting it to a too large value can produce an error as there need to be at least
|
CVP |
The number of cross-validation partitions to create (minimum is 2). Do use a CVP value which ensures that at least two samples from the smalest group are kept for testing at each fold. E.g. If you have 10 samples in the smalest of the 2 groups a CVP of 4 would be maximum. |
NF |
The maximum number of features that would make sense to consider using as predcitors in the models. NF should be less than the number of training samples. |
by |
The size of the step when searching for the number of features to include. By default th esearch starts with the top 2 features, and a number of "by" features are added up to NF. |
NR |
An integer number between 1 and Inf giving the number of times the cross-validation should be repeated to ensure a robust solution to the question: how many features to use as predictors in the model?. |
See cited documents for more details.
A list object containing one item for each possible combination between the elements of preprocs,
filters, and classifiers. Each item of the list contains the following information:
predictions - a data frame with the predicted class membership belief value
(posterior probability) for each sample (row) and each class (column).
features - Names of the Affy probesets used as predictors by the model. A letter "F" is
added as suffix to the probeset names.
model - A fitted model object as produced by the lda, svm and kNN functions.
performanceTr - A matrix giving the number of features tested (NN) mean AUC over
all folds and repetitions (meanAUC), and the standard deviation of AUC values accross folds and
repeats of the cross-validation.
bestAUC - The value of mean AUC corresponding to the optimal number of features chosen.
Adi Laurentiu Tarca <[email protected]>
Adi L. Tarca, Mario Lauria, Michael Unger, Erhan Bilal, Stephanie Boue, Kushal Kumar Dey,
Julia Hoeng, Heinz Koeppl, Florian Martin, Pablo Meyer, Preetam Nandy, Raquel Norel,
Manuel Peitsch, Jeremy J Rice, Roberto Romero, Gustavo Stolovitzky, Marja Talikka,
Yang Xiang, Christoph Zechner, and IMPROVER DSC Collaborators,
Strengths and limitations of microarray-based phenotype prediction: Lessons learned
from the IMPROVER Diagnostic Signature Challenge. Bioinformatics, submitted 2013.
Tarca AL, Than NG, Romero R, Methodological Approach from the Best Overall
Team in the IMPROVER Diagnostic Signature Challenge, Systems Biomedicine, submitted, 2013.
library(maPredictDSC) library(LungCancerACvsSCCGEO) data(LungCancerACvsSCCGEO) anoLC gsLC table(anoLC$group) #run a series of methods combinations modlist=predictDSC(ano=anoLC,celfile.path=system.file("extdata/lungcancer",package="LungCancerACvsSCCGEO"), annotation="hgu133plus2.db", preprocs=c("rma"),filters=c("mttest","wilcox"),FCT=1.0,classifiers=c("LDA","kNN"), CVP=2,NF=4, NR=1) #rank combinations by the performance on training data (AUC) trainingAUC=sort(unlist(lapply(modlist,"[[","best_AUC")),decreasing=TRUE) trainingAUC #optional step; since we know the class of the test samples, let's see how the #methods combinations perform on the test data perfTest=function(out){ perfDSC(pred=out$predictions,gs=gsLC) } testPerf=t(data.frame(lapply(modlist,perfTest))) testPerf=testPerf[order(testPerf[,"AUC"],decreasing=TRUE),] testPerf #aggregate predictions from top 3 combinations of methods best3=names(trainingAUC)[1:3] aggpred=aggregateDSC(modlist[best3]) #test the aggregated model on the test data perfDSC(aggpred,gsLC)library(maPredictDSC) library(LungCancerACvsSCCGEO) data(LungCancerACvsSCCGEO) anoLC gsLC table(anoLC$group) #run a series of methods combinations modlist=predictDSC(ano=anoLC,celfile.path=system.file("extdata/lungcancer",package="LungCancerACvsSCCGEO"), annotation="hgu133plus2.db", preprocs=c("rma"),filters=c("mttest","wilcox"),FCT=1.0,classifiers=c("LDA","kNN"), CVP=2,NF=4, NR=1) #rank combinations by the performance on training data (AUC) trainingAUC=sort(unlist(lapply(modlist,"[[","best_AUC")),decreasing=TRUE) trainingAUC #optional step; since we know the class of the test samples, let's see how the #methods combinations perform on the test data perfTest=function(out){ perfDSC(pred=out$predictions,gs=gsLC) } testPerf=t(data.frame(lapply(modlist,perfTest))) testPerf=testPerf[order(testPerf[,"AUC"],decreasing=TRUE),] testPerf #aggregate predictions from top 3 combinations of methods best3=names(trainingAUC)[1:3] aggpred=aggregateDSC(modlist[best3]) #test the aggregated model on the test data perfDSC(aggpred,gsLC)