 Methodology article
 Open Access
 Published:
IPCARF: improving lncRNAdisease association prediction using incremental principal component analysis feature selection and a random forest classifier
BMC Bioinformatics volume 22, Article number: 175 (2021)
Abstract
Background
Identifying lncRNAdisease associations not only helps to better comprehend the underlying mechanisms of various human diseases at the lncRNA level but also speeds up the identification of potential biomarkers for disease diagnoses, treatments, prognoses, and drug response predictions. However, as the amount of archived biological data continues to grow, it has become increasingly difficult to detect potential human lncRNAdisease associations from these enormous biological datasets using traditional biological experimental methods. Consequently, developing new and effective computational methods to predict potential human lncRNA diseases is essential.
Results
Using a combination of incremental principal component analysis (IPCA) and random forest (RF) algorithms and by integrating multiple similarity matrices, we propose a new algorithm (IPCARF) based on integrated machine learning technology for predicting lncRNAdisease associations. First, we used two different models to compute a semantic similarity matrix of diseases from a directed acyclic graph of diseases. Second, a characteristic vector for each lncRNAdisease pair is obtained by integrating disease similarity, lncRNA similarity, and Gaussian nuclear similarity. Then, the best feature subspace is obtained by applying IPCA to decrease the dimension of the original feature set. Finally, we train an RF model to predict potential lncRNAdisease associations. The experimental results show that the IPCARF algorithm effectively improves the AUC metric when predicting potential lncRNAdisease associations. Before the parameter optimization procedure, the AUC value predicted by the IPCARF algorithm under 10fold crossvalidation reached 0.8529; after selecting the optimal parameters using the grid search algorithm, the predicted AUC of the IPCARF algorithm reached 0.8611.
Conclusions
We compared IPCARF with the existing LRLSLDA, LRLSLDALNCSIM, TPGLDA, NPCMF, and ncPred prediction methods, which have shown excellent performance in predicting lncRNAdisease associations. The compared results of 10fold crossvalidation procedures show that the predictions of the IPCARF method are better than those of the other compared methods.
Background
Bioinformatics has received increasing attention from both the public and the scientific community as biomedicine and sequencing technology developed. In bioinformatics, regions of the human genome that do not encode protein sequences are usually transcribed as noncoding RNAs (ncRNAs) [1]. Based on the length of such transcripts, ncRNAs can be partitioned into small ncRNAs and long ncRNAs (lncRNAs). The difference is that lncRNAs are more than 200 nucleotides in length [2], and they comprise the vast majority of noncoding RNAs. In recent years, lncRNAs have attracted wide attention from researchers. Increasing evidence indicates that lncRNAs usually play carcinogenic or tumour suppressor roles in human cancers [3, 4], including prostate cancer [5], hepatocellular carcinoma (HCC) [6] , colon cancer [7] , lung cancer [8], bladder cancer [9], and others.
lncRNAs have attracted wide attention from researchers in recent years. However, many lncRNA characteristics are still unclear, including their transcriptional regulation, structures, various biological processes or functions, and the molecular mechanisms of various diseases. At present, some new lncRNAs are discovered every year. This increasing number of lncRNAs has made using biological experimental methods for identifying lncRNAdisease associations more challenging. The use of biological experiments to identify lncRNAdisease associations introduces bottlenecks due to their experimental time and cost requirements. Thus, predicting potential lncRNAdisease associations through computational methods could effectively reduce the screening range of biological experiments, thereby also reducing the time and cost of biological experiments. In addition, using predictive calculation methods will help to discover the causes and mechanisms of diseases as soon as possible, which is highly important in disease diagnosis, drug prognosis, and target discovery.
As this research field has deepened, several lncRNAdisease association databases have been compiled. The LncRNADisease [10] is an lncRNAdisease association database established in 2013, and it was the first database in this area. Lnc2Cancer [11] was established in 2015; this dataset mainly includes data associations between cancer and lncRNAs. Compared with LncRNADisease, the entries in Lnc2Cancer are more comprehensive and complete. NONCODE [12] is a comprehensive knowledge base containing almost all ncRNAs, and LNCipedia [13] is a comprehensive human lncRNA database. By integrating a variety of data, the current version contains 120,353 human lncRNA transcripts. Moreover, it provides a tool for predicting proteincoding capabilities.
A semisupervised learning scheme called Laplacian regularized least squares for lncRNAdisease association (LRLSLDA) was proposed by Chen et al. [14] to predict new human lncRNAdisease associations. This was the first study to automatically predict lncRNAdisease associations. Later, Chen Xing made some improvements based on the LRLSLDA model. Sun et al. [15] proposed a global networkbased computing framework (RWRlncD), in which a potential lncRNAdisease association is predicted by executing a random walk with restart (RWR) method on the lncRNA functional similarity network. A method for predicting potential lncRNAdisease associations by constructing lncRNAdisease association networks and rnRNAdisease bipartite networks was proposed by Yang et al. [16]. In 2015, a new hypergeometric distribution model (HGLDA) was developed by Chen et al. [1] to predict potential lncRNAdisease associations. Zhou et al. [17] proposed the RWRHLD method, which integrated the miRNArelated lncRNAlncRNA crosstalk network, the disease similarity network, and the known lncRNAdiseaserelated network into a new network and then predicted potential lncRNAdisease associations based on the integrated network.
The above prediction models provide different perspectives and research ideas for the predicting lncRNAdisease associations and usher in the beginning of lncRNAdisease prediction. These methods provided reference data for the study of disease mechanisms and the functions of lncRNAs. However, the existing models still have some shortcomings; they are complex, suffer from high computational complexity, and neglect parameter selection. Therefore, considerable research on lncRNAdisease association prediction remains to be conducted.
The existing methods for predicting the lncRNAdisease associations have achieved solid results, but they have some limitations, and much room still exists for improvement. In this study, we develop a new automated method for predicting lncRNAdisease associations based on incremental principal component analysis (IPCA) and random forest (RF) technology, which we named IPCARF. First, we integrated disease semantic similarity, lncRNA functional similarity, and Gaussian interaction spectrum kernel similarity to obtain characteristic vectors of lncRNAdisease pairs. Second, we apply the IPCA method to effectively reduce the feature dimension of the dataset and obtain the best feature subspace from the original feature set. Finally, we train an RF model to predict potential lncRNAdisease associations.
Results
All the experiments were done in the Python 3.7 software on the Keras library with a TensorFlow background.
Selecting a classification algorithm
To choose an optimal classifier, we first compared the prediction results of several classic classifier algorithms on the experimental dataset. We compared RF classifiers with logistic regression (LR), knearest neighbor (KNN), linear discriminant analysis (LDA), naive bayes (NB), and support vector machine (SVM) algorithms. The parameters of all the algorithms were temporarily used as default parameter values.
First, we calculated and visualized confusion matrices based on the results of the six types of algorithms. The results are shown in Fig. 1. The horizontal axes of these confusion matrices denote the predicted label values, and the vertical axes denote the true label values. The dark colour on the diagonals indicates the classification accuracy. The darker the colour, the higher the accuracy. Figure 1 intuitively shows that among the six classification algorithms, the RF algorithm obtains the best results.
Crossvalidation is a commonly used method in machine learning that can greatly reduce errors caused by sample selection. In our experiments, we used 10fold crossvalidation (10CV) to assess the classification prediction ability of six different classification algorithms. The detailed results of these six different methods are shown in Fig. 2, where (a)–(e) show that the accuracy, precision, recall, F1score, and AUC values predicted by the RF algorithm are 0.868, 0.825, 0.916, 0.868, and 0.8147, respectively. Among the six algorithms, the RF algorithm achieves the highest values on all five evaluation indicators.
In the experiment, we also recorded the execution times of the six algorithms to compare and evaluate the runtime efficiency of each algorithm. The runtime comparison chart for the six algorithms in Fig. 2f shows that the SVM algorithm has the longest execution time, while the NB algorithm has the shortest, but the prediction results of these algorithms (such as the accuracy of the NB algorithm) are not as good as those of the RF algorithm. Therefore, we choose the RF algorithm as the experimental classifier. Figure 3 shows a box plot of the prediction results of the six classifiers using 10CV.
The results are further verified based on the experimental results shown in Fig. 3. The RF algorithm obtains the best prediction results among the six algorithms. Therefore, in our model, we chose the RF algorithm to integrate with the IPCA method to predict lncRNAdisease associations.
Comparison of the proposed IPCARF and the traditional RF algorithm
Through the above experiment, we selected the RF classifier as the classifier in the improved algorithm. Next, we used the IPCA algorithm to improve the performance of the RF classifier. We compared the prediction effect of the IPCARF algorithm with that of the traditional RF algorithm using 10CV. The experimental results are shown in Fig. 4, which shows that the accuracy, precision, recall, and F1score values obtained when using the IPCARF algorithm for prediction are higher than those obtained when using only the RF algorithm for prediction. The ROC curve results verify that the prediction result of the IPCARF method is better than that of the RF method. In addition, the runtime of the IPCARF algorithm is lower than that of the RF. Therefore, it can be concluded that introducing the IPCA algorithm into the RF model effectively improves the performance of the classifier.
Discussion
Analysis of parameters
In the above experiment, we did not consider the effect of different parameter values on the prediction results of the algorithms; we used the default parameter settings for all the algorithms. In practical applications, after selecting a suitable model, the parameter settings are particularly important Because different parameters have different effects on model predictive ability.
The parameters used in IPCARF also affect its prediction performance. We have performed many experiments and found that, except for the n_estimators parameter, changes in the other parameters have relatively little impact on the prediction results of IPCARF. Therefore, here, we consider only the influence of the n_estimator parameter on the prediction results of the IPCARF algorithm. In this experiment, we set the value range of the n_estimators parameter to [100, 500, 1000, 1500, 2000, and 2500]; then, we selected the optimal n_estimator parameter value using the grid search (GS) method.
The grid search method is a commonly used parameter optimization algorithm [18]. A grid search is a method of finding parameters. Its core principle is to first define the parameter area to be searched and then divide the area into grids. The intersections in the grid form the parameter combinations to be searched. In other words, all the intersections in the grid are parameter combinations (c, g) that should be searched, and each combination (c, g) is retrieved during the grid search process. To obtain the best (c, g) combination, the kfold method is used to test the classification accuracy of each group (c, g), and the group with the highest accuracy among all selected (c, g) is selected as the parameters for building the model.
In our experiment, the best n_estimator parameter value found after executing the GS algorithm was 1500. Thus, we adopt n_estimators = 1500 to further compare the execution performances of the IPCARF and RF algorithms. The experimental results are shown in Fig. 5.
Figure 5a–d displays the accuracy, precision, recall, and F1score results of the two algorithms. Figure 5e shows that the AUC values predicted by the two algorithms are 0.8257 and 0.8611, and Fig. 5f shows that the running time of the IPCAFR algorithm is significantly lower than that of the RF algorithm.
Comparisons with existing works
Previous scholars have developed many effective prediction methods for the prediction of lncRNAdisease associations. However, because the data themselves have problems such as instability and because the evaluation methods used by various methods are inconsistent, the current methods still leave considerable room for improvement. To further verify the effect of IPCARF, we compared it with five other existing works, including LRLSLDA [14], LRLSLDALNCSIM [1], TPGLDA [19], NPCMF [20], and ncPred [21].The comparison results showing the AUC values of these algorithms are shown in Fig. 6.
Figure 6 shows that the AUC value obtained when using the IPCARF method to predict lncRNAdisease associations is better than that of the other comparison algorithms. Because of the instability of genetic data, the results of each experimental run differ to some degree. Consequently, we repeated the experiment 10 times and took the average as the final result. In the experiment, the highest value of AUC obtained when running the IPCARF algorithm was 0.906, and the lowest value was 0.861. These experimental results indicate that the prediction performance of the IPCARF method is slightly better than that of the comparative methods.
Case study
Lung cancer is a common malignant lung tumor. The top 5 long noncoding RNAs that use the IPCARF algorithm to predict lung cancer are: GAS5,XIST,CDKN2BAS1, PVT1 and HOTAIR. Four of the top 5 have the latest literature to verify. Ranked No. 1 is GAS5, and the research in the literature [22] shows that GAS5 may play a role in suppressing cancer. Ranked No. 2 is XIST, and the research in the literature [23] shows that XIST plays an important regulatory role in cancer biology. Ranked No. 4 is PVT1, and the research in the literature [24] shows that PVT1 can inhibit cell proliferation, migration and invasion. Ranked No. 5 is HOTAIR, and the literature [25] found that HOTAIR affects the drug resistance of small cell lung cancer cells by regulating the methylation of HOXA1.
Conclusions
Biological experiments have continuously been the primary means of identifying lncRNAdisease associations. However, the number of newly discovered lncRNAs increases every year, and this growing amount of data functions as a bottleneck to the experimental identification methods. Fortunately, several publicly available databases have emerged that have introduced greater opportunities for predicting potential lncRNAdisease associations through computational methods. Using computational methods to predict potential lncRNAdisease associations is important, because such associations can effectively improve our understanding of disease pathogenesis and guide treatments. In this study, we proposed a novel model called IPCARF to predict lncRNAdisease associations and compared it with the existing LRLSLDA, LRLSLDALNCSIM, TPGLDA, NPCMF, and ncPred prediction methods using 10CV. These methods have achieved excellent performances for predicting lncRNAdisease associations. The comparison results show that the prediction results of the IPCARF method are better than those of the compared methods.
Although the IPCARF method has achieved good prediction results, it still has some limitations that should be improved in future studies. First, the experimental data are still not rich enough, which limits the predicted results. As more data related to lncRNA diseases becomes available, the IPCARF method will improve. The complexity and inconsistency of biological data also cause certain difficulties in improving and comparing algorithms, especially the inability to obtain completely consistent data sources. In future work, we will consider integrating data from different sources to improve the prediction performance of IPCARF by improving the integrity and quality of the experimental data.
Methods
Data collection
Disease similarity data
The data on disease similarity compiled by different scientific researchers are not the same. Among them, the data compiled by van Driel et al. [26] is the most often cited; it is also the most recognized and is considered to be relatively authoritative disease similarity data. A similarity network of 5080 human genetic diseases is constructed by this database, which is available at http://www.cmbi.ru.nl/MimMiner/. The database has a matrix file format.
lncRNAdisease association data
In 2013, Chen et al. [10] established the LncRNADisease database (http://210.73.221.6/lncrnadisease), which was the first database of lncRNAdisease association data, and it was manually collected and experimentally verified. Over time and the continuous expansion of lncRNA research, the LncRNADisease database has also continuously expanded, and the number of entries increases yearly. In this study, we used the v2017 data from the LncRNADisease database. The datasets generated and analyzed during the current study are presented in Additional file 1.
Disease semantic similarity
Disease semantic similarity model
Referring to the calculation method in [1], two models are used on the directed acyclic graph (DAG) of diseases to compute a disease semantic similarity score.
First, the contribution of the disease term t in DAG(D) to the semantic value of disease D is defined as follows:
where \(\Delta\) represents a semantic contribution attenuation factor.
Then, all the contributions of the ancestral disease and disease D itself are summed, and the semantic value of disease D is defined as follows:
The semantic similarity between two diseases \(D_1\) and \(D_2\) is defined as follows:
where sim1 denotes the disease semantic similarity matrix.
Moreover, the method for calculating disease similarity refers to the calculation method proposed in [27], which provides a detailed description.
Gaussian interaction profile kernel similarity for disease
Similar diseases may have similar related lncRNAs. The similarity of Gaussian interaction kernels can be computed from the known lncRNAdisease association network. The Gaussian interaction kernel similarity between diseases D1 and D2 is computed as follows:
where \(k_{dis}\) represents the standardized core width, which is calculated by
where m represents the disease number.
Gaussian interaction profile kernel similarity for lncRNA
The Gaussian interaction kernel similarity between lncRNAs \(L_1\) and \(L_2\) is computed as
where n represents the lncRNA number.
The IPCA algorithm
The PCA algorithm
Principal Component Analysis (PCA) is a commonly used data analysis algorithm and an unsupervised linear feature extraction algorithm. PCA has been widely used in applications such as lossy data compression, feature selection, and dimensionality reduction [28]. PCA methods can reduce data from a highdimensional space to a lowdimensional space because it merges similar features due to the variance. Thus, PCA can reduce both data and the number of data features, which helps to prevent model overfitting.
The main idea underlying the PCA algorithm is to describe things using fewer data features that represent most of the main information. PCA is a statistical method that recombines characteristic variables with linear associations into fewer characteristic variables. The PCA algorithm is essentially a transformation of the variables that introduces a set of new variables that are not related to the original variables; instead, these new variables are linear functions of the original variables. Each new variable is called a principal component. This group of principle is sorted based on variance; the first principal component is the one with the largest variance in the linear function. The second principal component is the linear function with the secondlargest variance, and the first and second principal components are not correlated with each other. The third principal component is also uncorrelated with the first and second principal components and constitutes the linear function with the thirdlargest variance. By analogy, the original data are transformed using \(KL\) to obtain new data after dimensionality reduction.
Assume that the size of the original data sample matrix is \(m\times n\). The matrix has m dimensions, and each dimension has n samples. The sample matrix [29] can be expressed as follows:
Find the zeroaverage of each row in the matrix D , that is, subtract the average value of each column, expressed as follows:
where \(a_{i}\) represents the average of each column of samples, expressed as follows:
Then, calculate the covariance matrix of the sample matrix. For an \(m\times n\) sample matrix, the covariance matrix C is an \(m\times m\) matrix, and each element \(C_{ij}\) of the covariance matrix represents the covariance of the variable \(d_{i},d_{j}\).
Next, compute the eigenvalues of the covariance matrix and sort the calculated eigenvalues in descending order. The eigenvectors relevant to the first k eigenvalues are adopted to form a new matrix.
Finally, the projection of the original data sample matrix D on the new eigenvector matrix is calculated to obtain the data eigenvectors after dimensionality reduction.
The IPCA algorithm
The IPCA algorithm mainly improves the covariance matrix and reconstructs the original covariance matrix into a lowdimensional matrix that retains most of the information of the original covariance matrix.
First, the \(l_{2}\text {}norm\) of each column vector of the original covariance matrix is calculated as follows:
Next, form a new matrix B with the largest top k column vectors in the obtained norm.
Perform QR decomposition on the new matrix B to obtain the lowdimensional matrix C1.
Perform singular value decomposition on the C1 matrix. Arrange the obtained singular value representations in order of importance, discard the unimportant eigenvectors, and retain the eigenvalues of the data set after dimensionality reduction.
In short, in the IPCA algorithm, the singular value decomposition of the central data is used for linear dimensionality reduction, and only the most important singular vectors are retained to project the data into a lowerdimensional space.
The RF classification algorithm
The RF classification algorithm belongs to the supervised learning subfield of the machine learning field. It uses samples from a dataset for training and the trained model is applied to perform predictions on real data to evaluate whether the results meet expectations.
The traditional classification algorithms mainly include knearest neighbour (KNN) [30] algorithms, naive Bayes (NB) [31] algorithms, decision tree algorithms and support vector machine (SVM) [32] algorithms. Most of these algorithms are relatively mature, and each has a range of suitable application scenarios, but they also leave space for corresponding algorithm classification performance improvements. The decision tree algorithm is a type of split tree approach based on data attribute characteristics. As research has deepened, improved decision trees such as ID3, C4.5, classification and regression tree (CART), and regression trees have gradually been developed. The decision tree algorithm has advantages such as an easy way to understand the decision results and powerful functions, but it may exhibit problems such as weak fitting. The NB algorithm comes from the field of statistics and predicts the posterior probability based on the prior probability. The advantage of the NB algorithm is its fast calculation speed, while its disadvantage is that there may be dependencies between attributes, which often leads to lower classification accuracy. The SVM algorithm performs highdimensional and nonlinear classification by constructing a hyperplane. The advantages of the SVM algorithm are that it is highly efficient and provides good classification accuracy. Its disadvantages are the complex structure of its kernel function and a lack of data sensitivity.
The RF method, first proposed by Breiman [33]is a machine learning algorithm consisting of many decision trees. It is a combination of the Bagging [34] and Random Subspaces [35]methods. The RF algorithm [35] is considered to be an ensemble learning and supervised classification method. It first randomly establishes a forest composed of multiple unrelated decision trees; these multiple decision tree classifier models each learn and perform prediction separately. Then, the prediction results of the multiple decision tree classifier models are combined to obtain a final prediction result. There are two typical ways of combining the prediction results from different decision tree classifiers in RF. One is to average the prediction results of all the decision tree classifiers to obtain a prediction result for the entire forest. The other is to conduct a vote on the prediction results from all decision tree classifiers to select an optimal prediction result as the prediction result of the entire forest. A general flowchart of the RF algorithm is shown in Fig. 7.
The RF algorithm first selects n samples from the original training set as a training subset and then generates a decision tree for each subset. The above steps are repeated a total of n times to generate n decision trees that form the random forest. Finally, the random forest obtained by training is used to predict test samples, and an optimal classification result is selected using either the mean method or the voting method.
The hospital has a large amount of data after the diagnosis of the patient, how to extract the data that has a high correlation with the patient’s disease from this large and complex data set for analysis. If we can use some highperformance algorithms to efficiently classify these data and make predictions for some diseases, such as the predictive analysis of cancer and other diseases, it will have very important and farreaching significance. The data processed in the medical field are usually highdimensional, and many data sets are extremely unbalanced. Traditional analysis methods cannot get a good diagnosis effect. The random forest can efficiently process highdimensional data, so it is widely used in the medical field.
Long noncoding RNAdisease prediction based on IPCA and RF
In this study, we developed an algorithm called IPCARF based on the IPCA and RF methods. First, two semantic similarity matrices, a Gaussian kernel similarity matrix for diseases and a Gaussian kernel similarity matrix for lncRNAs are established. Second, a feature vector is extracted from the similarity matrix to construct an adjacency matrix. Then, the positive samples and negative samples are extracted from the adjacency matrix to construct the dataset for prediction. Next, the IPCA method is applied to select features and reduce the dataset dimensionality. Finally, the FR classifier is used to make predictions. The IPCARF process is shown in Fig. 8.
Evaluation metrics
To assess the potential classification prediction ability of the IPCARF algorithm, we adopted the metrics of precision, accuracy, F1score, recall, and the receiver operating characteristic (ROC) curve to represent the abilities of the six candidate algorithms. The calculation formulas for several of these metrics are defined below:
where TP is the number of positive samples correctly classified as positive samples by the classifier; TN is the number of negative samples correctly classified as negative samples by the classifier; FP is the number of negative samples incorrectly classified as positive samples by the classifier; and FN is the number of positive samples incorrectly classified as negative samples by the classifier.
Recall is the proportion of positive examples that are accurately predicted (it can be called TPR or recall), that is, the proportion of positive examples correctly predicted by the classification model to the total number of correctly classified samples. The higher the accuracy, precision, recall, and F1score are, the better the classification performance is.
The ROC curve is a characteristic of classifier performance. The abscissa of this curve is the false positive rate (FPR), and the ordinate is TPR (recall). The formula for calculating the FPR is shown below:
The area under the curve (AUC) represents the area under the ROC curve enclosed by the coordinate axis. The value of this area cannot exceed 1. Usually, the ROC curves are located above the straight line \(y=x\). Generally, the AUC value should range between 0.5 and 1. An AUC value closer to 1.0 represents a better classifier performance. An \(AUC <= 0.5\) has no application value. Because the ROCs evaluate model results in an objective manner, this metric is widely used in practical applications.
Availability of data and materials
This database is available at http://www.cuilab.cn/lncrnadisease. Source code is available at https://github.com/zhurong1942/IPCARF_zr1.
Abbreviations
 IPCA:

Incremental principal component analysis
 RF:

Random forests
 lncRNA:

Long noncoding RNA
 DAG:

Directed acyclic graph
 GS:

Grid search
 AUC:

Area under curve
 10CV:

10Fold crossvalidation
 ROC:

Receiver operating characteristic
 LR:

Logistic regression
 KNN:

Knearest neighbor
 NB:

Naive Bayes
 LDA:

Linear discriminant analysis
 SVM:

Support vector machine
 CART:

Classification and regression tree
 FN:

False negative
 FP:

False positive
 TN:

True negative
 TP:

True positive
 FPR:

False positive rate
 CART:

Classification and regression tree
 TCGA:

The Cancer Genome Atlas
 LRLSLDA:

Laplacian Regularized Least Squares for LncRNADisease Association
 LNCSIM:

lncRNA functional similarity calculation models
 TPGLDA:

lncRNAdiseasegene tripartite graph
 NPCMF:

Nearest profilebased collaborative matrix factorization
 ncPred:

ncRNAdisease association prediction
References
Chen X. Predicting lncRNAdisease associations and constructing lncRNA functional similarity network based on the information of miRNA. Sci Rep. 2015;5(1):13186–13186.
Ponting CP, Oliver PL, Reik W. Evolution and functions of long noncoding RNAs. Cell. 2009;136(4):629–41.
Youness RA, Gad MZ. Long noncoding RNAs: functional regulatory players in breast cancer. Noncoding RNA Res. 2019;4(1):36–44.
Taheri M, Omrani MD, Ghafourifard S. Long noncoding RNA expression in bladder cancer. Biophys Rev. 2018;10(4):1205–13.
Chung S, Nakagawa H, Uemura M, Piao L, Ashikawa K, Hosono N, Takata R, Akamatsu S, Kawaguchi T, Morizono T, et al. Association of a novel long noncoding rna in 8q24 with prostate cancer susceptibility. Cancer Sci. 2011;102(1):245–52.
Wang J, Liu X, Wu H, Ni P, Gu Z, Qiao Y, Chen N, Sun F, Fan Q. CREB upregulates long noncoding RNA, HULC expression through interaction with microRNA372 in liver cancer. Nucleic Acids Res. 2010;38(16):5366–83.
Pibouin L, Villaudy J, Ferbus D, Muleris M, Prosperi M, Remvikos Y, Goubin G. Cloning of the mRNA of overexpression in colon carcinoma1: a sequence overexpressed in a subset of colon carcinomas. Cancer Genet Cytogenet. 2002;133(1):55–60.
Zhang X, Zhou Y, Mehta KR, Danila DC, Scolavino S, Johnson SR, Klibanski A. A pituitaryderived MEG3 isoform functions as a growth suppressor in tumor cells. J Clin Endocrinol Metab. 2003;88(11):5119–26.
Zhang Z, Hao H, Zhang CJ, Yang XY, He Q, Lin J. Evaluation of novel gene UCA1 as a tumor biomarker for the detection of bladder cancer. Natl Med J China. 2012;92(6):384–7.
Chen G, Wang Z, Wang D, Qiu C, Liu M, Chen X, Zhang Q, Yan G, Cui Q. LncRNA disease: a database for longnoncoding RNAassociated diseases. Nucleic Acids Res. 2012;41:983–6.
Ning S, Zhang J, Wang P, Zhi H, Wang J, Liu Y, Gao Y, Guo M, Yue M, Wang L, et al. Lnc2cancer: a manually curated database of experimentally supported lncRNAs associated with various human cancers. Nucleic Acids Res. 2016;44:980–5.
Bu D, Yu K, Sun S, Xie C, Skogerbo G, Miao R, Xiao H, Liao Q, Luo H, Zhao G, et al. Noncode v30: integrative annotation of long noncoding RNAs. Nucleic Acids Res. 2012;40:210–5.
Volders P, Helsens K, Wang X, Menten B, Martens L, Gevaert K, Vandesompele J, Mestdagh P. Lncipedia: a database for annotated human lncRNA transcript sequences and structures. Nucleic Acids Res. 2013;41:246–51.
Chen X, Yan G. Novel human lncRNAdisease association inference based on lncRNA expression profiles. Bioinformatics. 2013;29(20):2617–24.
Sun J, Shi H, Wang Z, Zhang C, Liu L, Wang L, He W, Hao D, Liu S, Zhou M. Inferring novel lncRNAdisease associations based on a random walk model of a lncRNA functional similarity network. Mol BioSyst. 2014;10(8):2074–81.
Yang X, Gao L, Guo X, Shi X, Wu H, Song F, Wang B. A network based method for analysis of lncRNAdisease associations and prediction of lncRNAs implicated in diseases. PLOS ONE. 2014;9(1):e87797.
Zhou M, Wang X, Li J, Hao D, Wang Z, Shi H, Han L, Zhou H, Sun J. Prioritizing candidate diseaserelated long noncoding RNAs by walking on the heterogeneous lncRNA and disease network. Mol BioSyst. 2015;11(3):760–9.
Kennedy J, Eberhart R. Particle swarm optimization. In: Icnn95International Conference on Neural Networks. IEEE, 2002.
Ding L, Wang M, Sun D, Li A. TPGLDA: novel prediction of associations between lncRNAs and diseases via lncRNAdiseasegene tripartite graph. Sci Rep. 2018;8(1):1065–1065.
Gao Y, Cui Z, Liu J, Wang J, Zheng C. NPCMF: nearest profilebased collaborative matrix factorization method for predicting miRNAdisease associations. BMC Bioinform. 2019;20(1):1–10.
Alaimo S, Giugno R, Pulvirenti A. ncPred: ncRNAdisease association prediction through tripartite networkbased inference. Front Bioeng Biotechnol. 2014;2(71):71–71.
Shi X, Sun M, Liu H, Yao Y, Kong R, Chen F, Song Y. A critical role for the long noncoding RNA gas5 in proliferation and apoptosis in nonsmallcell lung cancer. Mol Carcinog. 2015;54:1–12. https://doi.org/10.1002/mc.22120.
Tantai J, Hu D, Yang Y, Geng J. Combined identification of long noncoding RNA XIST and HIF1AAS1 in serum as an effective screening for nonsmall cell lung cancer. Int J Clin Exp Pathol. 2015;8(7):7887–95.
Yang YR, Zang SZ, Zhong CL, Li YX, Zhao SS, Feng XJ. Increased expression of the incRNA PVT1 promotes tumorigenesis in nonsmall cell lung cancer. Int J Clin Exp Pathol. 2014;7(10):6929–35.
Fang S, Gao H, Tong Y, Yang J, Tang R, Niu Y, Li M, Guo L. Long noncoding RNAHOTAIR affects chemoresistance by regulating HOXA1 methylation in small cell lung cancer cells. Lab Invest. 2016;96(1):60–8. https://doi.org/10.1038/labinvest.2015.123.
Van Driel MA, Bruggeman J, Vriend G, Brunner HG, Leunissen JAM. A textmining analysis of the human phenome. Eur J Hum Genet. 2006;14(5):535–42.
Xuan P, Han K, Guo M, Guo Y, Li J, Ding J, Liu Y, Dai Q, Li J, Teng Z, et al. Prediction of microRNAs associated with human diseases based on weighted k most similar neighbors. PLOS ONE. 2013;8(8):e70204.
Lowe DG. Distinctive image features from scaleinvariant keypoints. Int J Comput Vision. 2004;60(2):91–110.
Luo J, Xiao Q, Liang C, Ding P. Predicting microRNAdisease associations using Kronecker regularized least squares based on heterogeneous omics data. IEEE Access. 2017;5:2503–13.
Nigsch F, Bender A, Van Buuren B, Tissen J, Nigsch EA, Mitchell JBO. Melting point prediction employing knearest neighbor algorithms and genetic parameter optimization. J Chem Inf Model. 2006;46(6):2412–22.
He Q, Shahabi H, Shirzadi A, Li S, Chen W, Wang N, Chai H, Bian H, Ma J, Chen Y, et al. Landslide spatial modelling using novel bivariate statistical based Naïve Bayes, RBF classifier, and RBF network machine learning algorithms. Sci Total Environ. 2019;663:1–15.
Cherkassky V. The nature of statistical learning theory. IEEE Trans Neural Netw. 1997;8(6):1564–1564.
Breiman L. Random forests. Mach Learn. 2001;45(1):5–32.
Breiman L. Bagging predictors. Mach Learn. 1996;24(2):123–40. https://doi.org/10.1007/BF00058655.
Ho TK. The random subspace method for constructing decision forests. IEEE Trans Pattern Anal Mach Intell. 1998;20(8):832–44.
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This work was supported by the Jiangsu Key Construction Laboratory of IoT Application Technology. This work is supported in part by the grants of the National Natural Science Foundation of China, Nos. 61902215, 61872220. The funding bodies played no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
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RZ and LYD performed the analysis and prepared the manuscript. YW designed the project and reviewed the manuscript. JXL designed and supervised the project and reviewed the manuscript. The authors read and approved the final version of the manuscript.
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Additional file 1
. LncRNA name, Disease name, Dysfunction type.
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Zhu, R., Wang, Y., Liu, JX. et al. IPCARF: improving lncRNAdisease association prediction using incremental principal component analysis feature selection and a random forest classifier. BMC Bioinformatics 22, 175 (2021). https://doi.org/10.1186/s12859021041049
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DOI: https://doi.org/10.1186/s12859021041049
Keywords
 LncRNAdisease
 Association prediction
 Incremental principal component analysis
 Random forests