scholarly journals EMSaov: An R Package for the Analysis of Variance with the Expected Mean Squares and its Shiny Application

The R Journal ◽  
2017 ◽  
Vol 9 (1) ◽  
pp. 252 ◽  
Author(s):  
Hye-Min Choe ◽  
Mijeong Kim ◽  
Eun-Kyung Lee
2018 ◽  
Author(s):  
Jianfeng Li ◽  
Bowen Cui ◽  
Yuting Dai ◽  
Ling Bai ◽  
Jinyan Huang

The number of bioinformatics resources, such as tools/scripts and databases are growing exponentially. This poses a great challenge for users to access, manage, and integrate the corresponding bioinformatics resources. To facilitate the request, we proposed a comprehensive R package, BioInstaller, which includes the R functions, Shiny application, and the HTTP representational state transfer (REST) application programming interfaces (APIs). We also established a community-based configuration pool to collect, access and share bioinformatics resources. The source code of BioInstaller is freely available at our lab website http://bioinfo.rjh.com.cn/labs/jhuang/tools/bioinstaller or popular package host GitHub at: https://github.com/JhuangLab/BioInstaller. Also, a docker image can be downloaded from DockerHub (https://hub.docker.com/r/bioinstaller).


2020 ◽  
Author(s):  
Na Liu ◽  
Yanhong Zhou ◽  
J. Jack Lee

Abstract BackgroundWhen applying secondary analysis on published survival data, it is critical to obtain each patient’s raw data, because the individual patient data (IPD) approach has been considered as the gold standard of data analysis. However, researchers often lack access to the IPD. We aim to propose a straightforward and robust approach to help researchers to obtain IPD from published survival curves with a friendly software platform. ResultsImproving upon the existing methods, we proposed an easy-to-use, two-stage approach to reconstruct IPD from published Kaplan-Meier (K-M) curves. Stage 1 extracts raw data coordinates and Stage 2 reconstructs IPD using the proposed method. To facilitate the use of the proposed method, we develop the R package IPDfromKM and an accompanied web-based Shiny application. Both the R package and Shiny application can be used to extract raw data coordinates from published K-M curves, reconstruct IPD from data coordinates extracted, visualize the reconstructed IPD, assess the accuracy of the reconstruction, and perform secondary analysis on the IPD. We illustrate the use of the R package and the Shiny application with K-M curves from published studies. Extensive simulations and real world data applications demonstrate that the proposed method has high accuracy and great reliability in estimating the number of events, number of patients at risk, survival probabilities, median survival times, as well as hazard ratios. ConclusionsIPDfromKM has great flexibility and accuracy to reconstruct IPD from published K-M curves with different shapes. We believe that the R package and the Shiny application will greatly facilitate the potential use of quality IPD data and advance the use of secondary data to make informed decision in medical research.


2019 ◽  
Vol 35 (22) ◽  
pp. 4827-4829 ◽  
Author(s):  
Xiao-Fei Zhang ◽  
Le Ou-Yang ◽  
Shuo Yang ◽  
Xing-Ming Zhao ◽  
Xiaohua Hu ◽  
...  

Abstract Summary Imputation of dropout events that may mislead downstream analyses is a key step in analyzing single-cell RNA-sequencing (scRNA-seq) data. We develop EnImpute, an R package that introduces an ensemble learning method for imputing dropout events in scRNA-seq data. EnImpute combines the results obtained from multiple imputation methods to generate a more accurate result. A Shiny application is developed to provide easier implementation and visualization. Experiment results show that EnImpute outperforms the individual state-of-the-art methods in almost all situations. EnImpute is useful for correcting the noisy scRNA-seq data before performing downstream analysis. Availability and implementation The R package and Shiny application are available through Github at https://github.com/Zhangxf-ccnu/EnImpute. Supplementary information Supplementary data are available at Bioinformatics online.


Author(s):  
Janina Reeder ◽  
Mo Huang ◽  
Joshua S Kaminker ◽  
Joseph N Paulson

Abstract Summary We developed the MicrobiomeExplorer R package to facilitate the analysis and visualization of microbial communities. The MicrobiomeExplorer R package allows a user to perform typical microbiome analytic workflows and visualize their results, either through the command line or an interactive Shiny application included with the package. In addition to applying common analytical workflows, the application enables automated analysis report generation. Availability and implementation Available at https://github.com/zoecastillo/microbiomeExplorer. Supplementary information Supplementary data are available at Bioinformatics online.


JAMIA Open ◽  
2021 ◽  
Vol 4 (3) ◽  
Author(s):  
David M Miller ◽  
Sophia Z Shalhout

Abstract Objectives Clinico-genomic data (CGD) acquired through routine clinical practice has the potential to improve our understanding of clinical oncology. However, these data often reside in heterogeneous and semistructured data, resulting in prolonged time-to-analyses. Materials and Methods We created GENETEX: an R package and Shiny application for text mining genomic reports from electronic health record (EHR) and direct import into Research Electronic Data Capture (REDCap). Results GENETEX facilitates the abstraction of CGD from EHR and streamlines the capture of structured data into REDCap. Its functions include natural language processing of key genomic information, transformation of semistructured data into structured data, and importation into REDCap. When evaluated with manual abstraction, GENETEX had >99% agreement and captured CGD in approximately one-fifth the time. Conclusions GENETEX is freely available under the Massachusetts Institute of Technology license and can be obtained from GitHub (https://github.com/TheMillerLab/genetex). GENETEX is executed in R and deployed as a Shiny application for non-R users. It produces high-fidelity abstraction of CGD in a fraction of the time.


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e5853 ◽  
Author(s):  
Jianfeng Li ◽  
Bowen Cui ◽  
Yuting Dai ◽  
Ling Bai ◽  
Jinyan Huang

The increase in bioinformatics resources such as tools/scripts and databases poses a great challenge for users seeking to construct interactive and reproducible biological data analysis applications. Here, we propose an open-source, comprehensive, flexible R package named BioInstaller that consists of the R functions, Shiny application, the HTTP representational state transfer application programming interfaces, and a docker image. BioInstaller can be used to collect, manage and share various types of bioinformatics resources and perform interactive and reproducible data analyses based on the extendible Shiny application with Tom’s Obvious, Minimal Language and SQLite format databases. The source code of BioInstaller is freely available at our lab website, http://bioinfo.rjh.com.cn/labs/jhuang/tools/bioinstaller, the popular package host GitHub, https://github.com/JhuangLab/BioInstaller, and the Comprehensive R Archive Network, https://CRAN.R-project.org/package=BioInstaller. In addition, a docker image can be downloaded from DockerHub (https://hub.docker.com/r/bioinstaller/bioinstaller).


2018 ◽  
Author(s):  
Jianfeng Li ◽  
Bowen Cui ◽  
Yuting Dai ◽  
Ling Bai ◽  
Jinyan Huang

The number of bioinformatics resources, such as tools/scripts and databases are growing exponentially. This poses a great challenge for users to access, manage, and integrate the corresponding bioinformatics resources. To facilitate the request, we proposed a comprehensive R package, BioInstaller, which includes the R functions, Shiny application, and the HTTP representational state transfer (REST) application programming interfaces (APIs). We also established a community-based configuration pool to collect, access and share bioinformatics resources. The source code of BioInstaller is freely available at our lab website http://bioinfo.rjh.com.cn/labs/jhuang/tools/bioinstaller or popular package host GitHub at: https://github.com/JhuangLab/BioInstaller. Also, a docker image can be downloaded from DockerHub (https://hub.docker.com/r/bioinstaller).


2021 ◽  
Vol 4 (1) ◽  
pp. 251524592095150
Author(s):  
Daniël Lakens ◽  
Aaron R. Caldwell

Researchers often rely on analysis of variance (ANOVA) when they report results of experiments. To ensure that a study is adequately powered to yield informative results with an ANOVA, researchers can perform an a priori power analysis. However, power analysis for factorial ANOVA designs is often a challenge. Current software solutions do not allow power analyses for complex designs with several within-participants factors. Moreover, power analyses often need [Formula: see text] or Cohen’s f as input, but these effect sizes are not intuitive and do not generalize to different experimental designs. We have created the R package Superpower and online Shiny apps to enable researchers without extensive programming experience to perform simulation-based power analysis for ANOVA designs of up to three within- or between-participants factors. Predicted effects are entered by specifying means, standard deviations, and, for within-participants factors, the correlations. The simulation provides the statistical power for all ANOVA main effects, interactions, and individual comparisons. The software can plot power across a range of sample sizes, can control for multiple comparisons, and can compute power when the homogeneity or sphericity assumption is violated. This Tutorial demonstrates how to perform a priori power analysis to design informative studies for main effects, interactions, and individual comparisons and highlights important factors that determine the statistical power for factorial ANOVA designs.


2021 ◽  
Vol 4 (1) ◽  
pp. 251524592096511
Author(s):  
Lisa M. DeBruine ◽  
Dale J. Barr

Experimental designs that sample both subjects and stimuli from a larger population need to account for random effects of both subjects and stimuli using mixed-effects models. However, much of this research is analyzed using analysis of variance on aggregated responses because researchers are not confident specifying and interpreting mixed-effects models. This Tutorial explains how to simulate data with random-effects structure and analyze the data using linear mixed-effects regression (with the lme4 R package), with a focus on interpreting the output in light of the simulated parameters. Data simulation not only can enhance understanding of how these models work, but also enables researchers to perform power calculations for complex designs. All materials associated with this article can be accessed at https://osf.io/3cz2e/ .


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