multiclassPairs: An R package to train multiclass pairbased classifier

Tumor Subtype ◽

Test Results ◽

Supplementary Data ◽

Classification Problems ◽

Excellent Performance ◽

Class Prediction

Abstract Motivation k–Top Scoring Pairs (kTSP) algorithms utilize in-sample gene expression feature pair rules for class prediction, and have demonstrated excellent performance and robustness. The available packages and tools primarily focus on binary prediction (i.e. two classes). However, many real-world classification problems e.g., tumor subtype prediction, are multiclass tasks. Results Here, we present multiclassPairs, an R package to train pair-based single sample classifiers for multiclass problems. multiclassPairs offers two main methods to build multiclass prediction models, either using a one-vs-rest kTSP scheme or through a novel pair-based Random Forest approach. The package also provides options for dealing with class imbalances, multiplatform training, missing features in test data, and visualization of training and test results. Availability ‘multiclassPairs’ package is available on CRAN servers and GitHub: https://github.com/NourMarzouka/multiclassPairs Supplementary information Supplementary data are available at Bioinformatics online.

PINSPlus: a tool for tumor subtype discovery in integrated genomic data

Bioinformatics ◽

10.1093/bioinformatics/bty1049 ◽

2018 ◽

Vol 35 (16) ◽

pp. 2843-2846 ◽

Cited By ~ 15

Author(s):

Hung Nguyen ◽

Sangam Shrestha ◽

Sorin Draghici ◽

Tin Nguyen

Keyword(s):

Personal Computer ◽

Genomic Data ◽

Omics Data ◽

Tumor Subtype ◽

Supplementary Data ◽

Significant Survival ◽

Survival Differences

Abstract Summary Since cancer is a heterogeneous disease, tumor subtyping is crucial for improved treatment and prognosis. We have developed a subtype discovery tool, called PINSPlus, that is: (i) robust against noise and unstable quantitative assays, (ii) able to integrate multiple types of omics data in a single analysis and (iii) dramatically superior to established approaches in identifying known subtypes and novel subgroups with significant survival differences. Our validation on 12,158 samples from 44 datasets shows that PINSPlus vastly outperforms other approaches. The software is easy-to-use and can partition hundreds of patients in a few minutes on a personal computer. Availability and implementation The package is available at https://cran.r-project.org/package=PINSPlus. Data and R script used in this manuscript are available at https://bioinformatics.cse.unr.edu/software/PINSPlus/. Supplementary information Supplementary data are available at Bioinformatics online.

DEsingle for detecting three types of differential expression in single-cell RNA-seq data

10.1101/173997 ◽

2017 ◽

Author(s):

Zhun Miao ◽

Ke Deng ◽

Xiaowo Wang ◽

Xuegong Zhang

Keyword(s):

Single Cell ◽

Differential Expression ◽

Negative Binomial ◽

Single Cells ◽

R Package ◽

Binomial Model ◽

Supplementary Data ◽

Rna Seq ◽

Real Zeros

AbstractSummaryThe excessive amount of zeros in single-cell RNA-seq data include “real” zeros due to the on-off nature of gene transcription in single cells and “dropout” zeros due to technical reasons. Existing differential expression (DE) analysis methods cannot distinguish these two types of zeros. We developed an R package DEsingle which employed Zero-Inflated Negative Binomial model to estimate the proportion of real and dropout zeros and to define and detect 3 types of DE genes in single-cell RNA-seq data with higher accuracy.Availability and ImplementationThe R package DEsingle is freely available at https://github.com/miaozhun/DEsingle and is under Bioconductor’s consideration [email protected] informationSupplementary data are available at bioRxiv online.

ngsReports: a Bioconductor package for managing FastQC reports and other NGS related log files

Bioinformatics ◽

10.1093/bioinformatics/btz937 ◽

2019 ◽

Vol 36 (8) ◽

pp. 2587-2588 ◽

Cited By ~ 10

Author(s):

Christopher M Ward ◽

Thu-Hien To ◽

Stephen M Pederson

Keyword(s):

Quality Control ◽

R Package ◽

Bioconductor Package ◽

Supplementary Data ◽

Large Sample ◽

Log Files ◽

Shiny App ◽

Next Generation Sequencing Ngs ◽

Generation Sequencing

Abstract Motivation High throughput next generation sequencing (NGS) has become exceedingly cheap, facilitating studies to be undertaken containing large sample numbers. Quality control (QC) is an essential stage during analytic pipelines and the outputs of popular bioinformatics tools such as FastQC and Picard can provide information on individual samples. Although these tools provide considerable power when carrying out QC, large sample numbers can make inspection of all samples and identification of systemic bias a challenge. Results We present ngsReports, an R package designed for the management and visualization of NGS reports from within an R environment. The available methods allow direct import into R of FastQC reports along with outputs from other tools. Visualization can be carried out across many samples using default, highly customizable plots with options to perform hierarchical clustering to quickly identify outlier libraries. Moreover, these can be displayed in an interactive shiny app or HTML report for ease of analysis. Availability and implementation The ngsReports package is available on Bioconductor and the GUI shiny app is available at https://github.com/UofABioinformaticsHub/shinyNgsreports. Supplementary information Supplementary data are available at Bioinformatics online.

iMIRAGE: an R package to impute microRNA expression using protein-coding genes

Bioinformatics ◽

10.1093/bioinformatics/btz939 ◽

2019 ◽

Vol 36 (8) ◽

pp. 2608-2610

Author(s):

Aritro Nath ◽

Jeremy Chang ◽

R Stephanie Huang

Keyword(s):

Gene Expression ◽

Small Rnas ◽

Transcriptional Regulators ◽

R Package ◽

Machine Learning Algorithms ◽

Expression Data ◽

Protein Coding ◽

Altered Protein ◽

Independent Test

Abstract Summary MicroRNAs (miRNAs) are critical post-transcriptional regulators of gene expression. Due to challenges in accurate profiling of small RNAs, a vast majority of public transcriptome datasets lack reliable miRNA profiles. However, the biological consequence of miRNA activity in the form of altered protein-coding gene (PCG) expression can be captured using machine-learning algorithms. Here, we present iMIRAGE (imputed miRNA activity from gene expression), a convenient tool to predict miRNA expression using PCG expression of the test datasets. The iMIRAGE package provides an integrated workflow for normalization and transformation of miRNA and PCG expression data, along with the option to utilize predicted miRNA targets to impute miRNA activity from independent test PCG datasets. Availability and implementation The iMIRAGE package for R, along with package documentation and vignette, is available at https://aritronath.github.io/iMIRAGE/index.html. Supplementary information Supplementary data are available at Bioinformatics online.

CPS analysis: self-contained validation of biomedical data clustering

Bioinformatics ◽

10.1093/bioinformatics/btaa165 ◽

2020 ◽

Vol 36 (11) ◽

pp. 3516-3521 ◽

Author(s):

Lixiang Zhang ◽

Lin Lin ◽

Jia Li

Keyword(s):

Data Clustering ◽

State Of The Art ◽

R Package ◽

Research Community ◽

Biomedical Data ◽

Data Generation ◽

Supplementary Data ◽

Point Set ◽

Class Labels

Abstract Motivation Cluster analysis is widely used to identify interesting subgroups in biomedical data. Since true class labels are unknown in the unsupervised setting, it is challenging to validate any cluster obtained computationally, an important problem barely addressed by the research community. Results We have developed a toolkit called covering point set (CPS) analysis to quantify uncertainty at the levels of individual clusters and overall partitions. Functions have been developed to effectively visualize the inherent variation in any cluster for data of high dimension, and provide more comprehensive view on potentially interesting subgroups in the data. Applying to three usage scenarios for biomedical data, we demonstrate that CPS analysis is more effective for evaluating uncertainty of clusters comparing to state-of-the-art measurements. We also showcase how to use CPS analysis to select data generation technologies or visualization methods. Availability and implementation The method is implemented in an R package called OTclust, available on CRAN. Contact [email protected] or [email protected] Supplementary information Supplementary data are available at Bioinformatics online.

RMTL: an R library for multi-task learning

Bioinformatics ◽

10.1093/bioinformatics/bty831 ◽

2018 ◽

Vol 35 (10) ◽

pp. 1797-1798 ◽

Cited By ~ 2

Author(s):

Han Cao ◽

Jiayu Zhou ◽

Emanuel Schwarz

Keyword(s):

Biological Networks ◽

Simulated Data ◽

R Package ◽

Low Rank ◽

Supplementary Data ◽

Software Environment ◽

Machine Learning Technique ◽

Task Learning ◽

Learning Technique

Abstract Motivation Multi-task learning (MTL) is a machine learning technique for simultaneous learning of multiple related classification or regression tasks. Despite its increasing popularity, MTL algorithms are currently not available in the widely used software environment R, creating a bottleneck for their application in biomedical research. Results We developed an efficient, easy-to-use R library for MTL (www.r-project.org) comprising 10 algorithms applicable for regression, classification, joint predictor selection, task clustering, low-rank learning and incorporation of biological networks. We demonstrate the utility of the algorithms using simulated data. Availability and implementation The RMTL package is an open source R package and is freely available at https://github.com/transbioZI/RMTL. RMTL will also be available on cran.r-project.org. Supplementary information Supplementary data are available at Bioinformatics online.

schex avoids overplotting for large single-cell RNA-sequencing datasets

Bioinformatics ◽

10.1093/bioinformatics/btz907 ◽

2019 ◽

Vol 36 (7) ◽

pp. 2291-2292 ◽

Author(s):

Saskia Freytag ◽

Ryan Lister

Keyword(s):

Single Cell ◽

Rna Sequencing ◽

R Package ◽

Supplementary Data ◽

Sequencing Data ◽

Single Cell Rna Sequencing

Abstract Summary Due to the scale and sparsity of single-cell RNA-sequencing data, traditional plots can obscure vital information. Our R package schex overcomes this by implementing hexagonal binning, which has the additional advantages of improving speed and reducing storage for resulting plots. Availability and implementation schex is freely available from Bioconductor via http://bioconductor.org/packages/release/bioc/html/schex.html and its development version can be accessed on GitHub via https://github.com/SaskiaFreytag/schex. Supplementary information Supplementary data are available at Bioinformatics online.

GladiaTOX: GLobal Assessment of Dose-IndicAtor in TOXicology

Bioinformatics ◽

10.1093/bioinformatics/btz187 ◽

2019 ◽

Vol 35 (20) ◽

pp. 4190-4192 ◽

Cited By ~ 4

Author(s):

Vincenzo Belcastro ◽

Stephane Cano ◽

Diego Marescotti ◽

Stefano Acali ◽

Carine Poussin ◽

...

Keyword(s):

Quality Control ◽

Data Processing ◽

Web Service ◽

Biomedical Research ◽

Global Assessment ◽

R Package ◽

High Content Screening ◽

Supplementary Data ◽

Severity Scores

Abstract Summary GladiaTOX R package is an open-source, flexible solution to high-content screening data processing and reporting in biomedical research. GladiaTOX takes advantage of the ‘tcpl’ core functionalities and provides a number of extensions: it provides a web-service solution to fetch raw data; it computes severity scores and exports ToxPi formatted files; furthermore it contains a suite of functionalities to generate PDF reports for quality control and data processing. Availability and implementation GladiaTOX R package (bioconductor). Also available via: git clone https://github.com/philipmorrisintl/GladiaTOX.git. Supplementary information Supplementary data are available at Bioinformatics online.

DataRemix: a universal data transformation for optimal inference from gene expression datasets

Bioinformatics ◽

10.1093/bioinformatics/btaa745 ◽

2020 ◽

Author(s):

Weiguang Mao ◽

Javad Rahimikollu ◽

Ryan Hausler ◽

Maria Chikina

Keyword(s):

Gene Expression ◽

R Package ◽

Eqtl Analysis ◽

Thompson Sampling ◽

Normalization Methods ◽

Special Cases ◽

Biological Signals ◽

Gene Correlation ◽

Value Decomposition

Abstract Motivation RNA-seq technology provides unprecedented power in the assessment of the transcription abundance and can be used to perform a variety of downstream tasks such as inference of gene-correlation network and eQTL discovery. However, raw gene expression values have to be normalized for nuisance biological variation and technical covariates, and different normalization strategies can lead to dramatically different results in the downstream study. Results We describe a generalization of singular value decomposition-based reconstruction for which the common techniques of whitening, rank-k approximation and removing the top k principal components are special cases. Our simple three-parameter transformation, DataRemix, can be tuned to reweigh the contribution of hidden factors and reveal otherwise hidden biological signals. In particular, we demonstrate that the method can effectively prioritize biological signals over noise without leveraging external dataset-specific knowledge, and can outperform normalization methods that make explicit use of known technical factors. We also show that DataRemix can be efficiently optimized via Thompson sampling approach, which makes it feasible for computationally expensive objectives such as eQTL analysis. Finally, we apply our method to the Religious Orders Study and Memory and Aging Project dataset, and we report what to our knowledge is the first replicable trans-eQTL effect in human brain. Availabilityand implementation DataRemix is an R package which is freely available at GitHub (https://github.com/wgmao/DataRemix). Supplementary information Supplementary data are available at Bioinformatics online.

RCytoGPS: An R Package for Reading and Visualizing Cytogenetics Data

Bioinformatics ◽

10.1093/bioinformatics/btab683 ◽

2021 ◽

Author(s):

Zachary B Abrams ◽

Dwayne G Tally ◽

Lynne V Abruzzo ◽

Kevin R Coombes

Keyword(s):

Large Scale ◽

International System ◽

Genetic Data ◽

R Package ◽

Supplementary Data ◽

Computational Tools ◽

Text Format ◽

Karyotype Analyses ◽

Computational Analyses

Abstract Summary Cytogenetics data, or karyotypes, are among the most common clinically used forms of genetic data. Karyotypes are stored as standardized text strings using the International System for Human Cytogenomic Nomenclature (ISCN). Historically, these data have not been used in large-scale computational analyses due to limitations in the ISCN text format and structure. Recently developed computational tools such as CytoGPS have enabled large-scale computational analyses of karyotypes. To further enable such analyses, we have now developed RCytoGPS, an R package that takes JSON files generated from CytoGPS.org and converts them into objects in R. This conversion facilitates the analysis and visualizations of karyotype data. In effect this tool streamlines the process of performing large-scale karyotype analyses, thus advancing the field of computational cytogenetic pathology. Availability and Implementation Freely available at https://CRAN.R-project.org/package=RCytoGPS. The code for the underlying CytoGPS software can be found at https://github.com/i2-wustl/CytoGPS. Supplementary information There is no supplementary data.