featureEvaluate {BioSeqClass} | R Documentation

## Evaluate Different Feature Coding Schemas

### Description

Feature sets from different feature coding schemas are used as input of classification models, and the model performance are given in the result.

### Usage

      featureEvaluate(seq, classLable, fileName, ele.type, featureMethod,
                cv=10, classifyMethod="libsvm",
                group=c("aaH", "aaV", "aaZ", "aaP", "aaF", "aaS", "aaE"), k, g,
                hydro.methods=c("kpm", "SARAH1"), hydro.indexs=c("hydroE", "hydroF", "hydroC"),
                aaindex.name, n, d, w=0.05, start.pos, stop.pos, psiblast.path,
                database.path, hmmpfam.path, pfam.path, Evalue=10^-5,
                na.type="all", na.strand="all", diprodb.method="all", diprodb.type="all",
                svm.kernel="linear", svm.scale=FALSE, svm.path, svm.options="-t 0",
                knn.k=1, nnet.size=2, nnet.rang=0.7, nnet.decay=0, nnet.maxit=100)

### Arguments

`seq` | a string vector for the protein, DNA, or RNA sequences.
`classLable` | a factor or vector for the class lable of sequences in seq.
`fileName` | a string for the output file name.
`ele.type` | a string for the type of biological sequence. This must be one of the strings "rnaBase", "dnaBase", "aminoacid" or "aminoacid2".
`featureMethod` | a string vector for the name of feature coding. The alternative names are "Binary", "CTD", "FragmentComposition", "GapPairComposition", "CKSAAP", "Hydro", "ACH", "AAindex", "ACI", "ACF", "PseudoAAComp", "PSSM", "DOMAIN", "BDNAVIDEO", and "DIPRODB".
`classifyMethod` | a string for the classification method. This must be one of the strings "libsvm", "svmlight", "NaiveBayes", "randomForest", "knn", "tree", "nnet", "rpart", "ctree", "ctreelibsvm", "bagging".
`cv` | an integer for the time of cross validation, or a string "leave\_one\_out" for the jacknife test.
`group` | a string vector for the group of amino acids. This alternative groups are: "aaH", "aaV", "aaZ", "aaP", "aaF", "aaS" or "aaE".
`k` | an integer indicating the length of sequence fragment (k>=1).
`g` | an integer indicating the distance between two aminoacids/bases (g>=0).
`hydro.methods` | a string vector for the methods of coding protein hydrophobic effect. This alternative groups are: "kpm" or "SARAH1".
`hydro.indexs` | a string vector for the methods of coding protein hydrophobic effect. This alternative groups are: "hydroE", "hydroF" or "hydroC".
`aaindex.name` | a string for the name of physicochemical and biochemical properties in AAindx.
`n` | an integer used as paramter of `featureACF` (1<=n<=L-2, L is the the length of sequence). featureACF takes the auto-correlation between fragment X(1)...X(L-m) and X(m+1)...X(L) (1<=m<=n) as features.
`d` | an integer used as paramter of `featurePseudoAAComp` (d>=1). Coupling between amino acids X(i) and X(i+d) are considered as features.
`w` | a numeric value for the weight factor of sequence order effect in `featurePseudoAAComp`.
`start.pos` | a integer vector denoting the start position of the fragment window. If it is missing, it is 1 by default.
`stop.pos` | a integer vector denoting the stop position of the fragment window. If it is missing, it is the length of sequence by default.
`psiblast.path` | a string for the path of PSI-BLAST program blastpgp. blastpgp will be employed to iteratively search database and generate position-specific scores for each position in the alignment.
`database.path` | a string for the path of formatted protein database. Database can be formatted by formatdb program.
`hmmpfam.path` | a string for the path of hammpfam program in HMMER. hammpfam will be employed to predict domains using models in Pfam database.
`pfam.path` | a string for the path of pfam domain database.
`Evalue` | a numeric value for the E-value cutoff of perdicted Pfam domain.
`na.type` | a string for nucleic acid type. It must be "DNA", "DNA/RNA", "RNA", or "all".
`na.strand` | a string for strand information. It must be "double", "single", or "all".
`diprodb.method` | a string for mode of property determination. It can be "experimental", "calculated", or "all".
`diprodb.type` | a string for property type. It can be "physicochemical", "conformational", "letter based", or "all".
`svm.kernel` | a string for kernel function of SVM.
`svm.scale` | a logical vector indicating the variables to be scaled.
`svm.path` | a character for path to SVMlight binaries (required, if path is unknown by the OS).
`svm.options` | Optional parameters to SVMlight. For further details see: "How to use" on http://svmlight.joachims.org/. (e.g.: "-t 2 -g 0.1"))
`nnet.size` | number of units in the hidden layer. Can be zero if there are skip-layer units.
`nnet.rang` | Initial random weights on [-rang, rang]. Value about 0.5 unless the inputs are large, in which case it should be chosen so that rang * max(|x|) is about 1.
`nnet.decay` | parameter for weight decay.
`nnet.maxit` | maximum number of iterations.
`knn.k` | number of neighbours considered in function `classifyModelKNN`.

### Details

`featureEvaluate` can test feature coding methods for short peptide, protein, DNA or RNA. It returns a ranked list based on the accuracy of classification result. Each element in the list has three components: "data", "model", and "performance". "data" is a data.frame object, which stores feature matrix and its last column is the class label. "model" is a vector for feature coding method, which contains 6 elements: "Feature\_Function", "Feature\_Parameter", "Feature\_Number", "Model", "Model\_Parameter", and "Cross_Validataion". "performance" is a vector for the performance result of classification model, which contains 10 elements: "tp", "tn", "fp", "fn", "prcc", "sn", "sp", "acc", "mcc", "pc".

### Author(s)

Hong Li

### Examples

      ## read positive/negative sequence from files.
      tmpfile1 = file.path(path.package("BioSeqClass"), "example", "acetylation_K.pos40.pep")
      tmpfile2 = file.path(path.package("BioSeqClass"), "example", "acetylation_K.neg40.pep")
      posSeq = as.matrix(read.csv(tmpfile1,header=FALSE,sep="\t",row.names=1))[,1]
      negSeq = as.matrix(read.csv(tmpfile2,header=FALSE,sep="\t",row.names=1))[,1]
      seq=c(posSeq,negSeq)
      classLable=c(rep("+1",length(posSeq)),rep("-1",length(negSeq)) )
      if(interactive()){
       ## test various feature coding methods.
       ## it may be time consuming.
        fileName = tempfile()
        testFeatureSet = featureEvaluate(seq, classLable, fileName, ele.type="aminoacid",
                  featureMethod=c("Binary", "CTD", "FragmentComposition", "GapPairComposition",
                  "Hydro"), cv=5, classifyMethod="libsvm",
                  group=c("aaH", "aaV", "aaZ", "aaP", "aaF", "aaS", "aaE"), k=3, g=7,
                  hydro.methods=c("kpm", "SARAH1"), hydro.indexs=c("hydroE", "hydroF", "hydroC") )
        summary = read.csv(fileName,sep="\t",header=T)
        fix(summary)

        ## Evaluate features from different feature coding functions
        feature.index = 1:5
        tmp <- testFeatureSet[[1]]$data
        colnames(tmp) <- paste(testFeatureSet[[feature.index[1]]]$model["Feature_Function"],testFeatureSet[[feature.index[1]]]$model["Feature_Parameter"],colnames(tmp),sep=" ; ")
        data <- tmp[,-ncol(tmp)]
        for(i in 2:length(feature.index) ){
          tmp <- testFeatureSet[[feature.index[i]]]$data
          colnames(tmp) <- paste(testFeatureSet[[feature.index[i]]]$model["Feature_Function"],testFeatureSet[[feature.index[i]]]$model["Feature_Parameter"],colnames(tmp),sep=" ; ")
          data <- data.frame(data, tmp[,-ncol(tmp)] )
        }
        name <- colnames(data)
        data <- data.frame(data, tmp[,ncol(tmp)] )
        ## feature forward selection by 'cv_FFS_classify'
        ## it is very time consuming.
        combineFeatureResult = fsFFS(data,stop.n=50,classifyMethod="knn",cv=5)
        tmp = sapply(combineFeatureResult,function(x){c(length(x$features),x$performance["acc"])})
        plot(tmp[1,],tmp[2,],xlab="featureNumber",ylab="Accuracy",main="result of FFS_KNN",pch=19)
        lines(tmp[1,],tmp[2,])

        ## compare the prediction accuracy based on different feature coding methods and different classification models.
        ## it is very time consuming.
        testResult = lapply(c("libsvm", "randomForest", "knn", "tree"),
          function(x){
                  tmp = featureEvaluate(seq, classLable, fileName = tempfile(),
                  ele.type="aminoacid", featureMethod=c("Binary", "CTD", "FragmentComposition",
                  "GapPairComposition", "Hydro"), cv=5, classifyMethod=x,
                  group=c("aaH", "aaV", "aaZ", "aaP", "aaF", "aaS", "aaE"), k=3, g=7,
                  hydro.methods=c("kpm", "SARAH1"), hydro.indexs=c("hydroE", "hydroF", "hydroC") );
                  sapply(tmp,function(y){c(y$model[["Feature_Function"]], y$model[["Feature_Parameter"]], y$model[["Model"]], y$performance[["acc"]])})
        })
        tmpFeature = as.factor(c(sapply(testResult,function(x){apply(x[1:2,],2,function(y){paste(y,collapse="; ")})})))
        tmpModel = as.factor(c(sapply(testResult,function(x){x[3,]})))
        tmp1 = data.frame(as.integer(tmpFeature), as.integer(tmpModel), as.numeric(c(sapply(testResult,function(x){x[4,]}))) )
        require(scatterplot3d)
        s3d=scatterplot3d(tmp1,color=c("red","blue","green","yellow")[tmp1[,2]],pch=19,
            xlab="Feature Coding", ylab="Classification Model",
            zlab="Accuracy under 5-fold cross validation",lab=c(10,6,7),
            y.ticklabs=c("",as.character(sort(unique(tmpModel))),"") )
      }

[Package BioSeqClass version 1.45.0 Index]