Reproducible home ranges (rhr): A new, user-friendly R package for analyses of wildlife telemetry data

2015 ◽  
Vol 39 (2) ◽  
pp. 358-363 ◽  
Author(s):  
Johannes Signer ◽  
Niko Balkenhol
Keyword(s):  
R Package ◽  
Home Ranges ◽  
Telemetry Data ◽  
User Friendly ◽  
Wildlife Telemetry

scholarly journals DIscBIO: A User-Friendly Pipeline for Biomarker Discovery in Single-Cell Transcriptomics

2021 ◽  
Vol 22 (3) ◽  
pp. 1399
Author(s):  
Salim Ghannoum ◽  
Waldir Leoncio Netto ◽  
Damiano Fantini ◽  
Benjamin Ragan-Kelley ◽  
Amirabbas Parizadeh ◽  
...  
Keyword(s):  
Single Cell ◽  
Biomarker Discovery ◽  
Enrichment Analysis ◽  
Myxoid Liposarcoma ◽  
R Package ◽  
Differential Analysis ◽  
A Cell ◽  
Reproducible Analysis ◽  
Transcriptomic Level ◽  
User Friendly

The growing attention toward the benefits of single-cell RNA sequencing (scRNA-seq) is leading to a myriad of computational packages for the analysis of different aspects of scRNA-seq data. For researchers without advanced programing skills, it is very challenging to combine several packages in order to perform the desired analysis in a simple and reproducible way. Here we present DIscBIO, an open-source, multi-algorithmic pipeline for easy, efficient and reproducible analysis of cellular sub-populations at the transcriptomic level. The pipeline integrates multiple scRNA-seq packages and allows biomarker discovery with decision trees and gene enrichment analysis in a network context using single-cell sequencing read counts through clustering and differential analysis. DIscBIO is freely available as an R package. It can be run either in command-line mode or through a user-friendly computational pipeline using Jupyter notebooks. We showcase all pipeline features using two scRNA-seq datasets. The first dataset consists of circulating tumor cells from patients with breast cancer. The second one is a cell cycle regulation dataset in myxoid liposarcoma. All analyses are available as notebooks that integrate in a sequential narrative R code with explanatory text and output data and images. R users can use the notebooks to understand the different steps of the pipeline and will guide them to explore their scRNA-seq data. We also provide a cloud version using Binder that allows the execution of the pipeline without the need of downloading R, Jupyter or any of the packages used by the pipeline. The cloud version can serve as a tutorial for training purposes, especially for those that are not R users or have limited programing skills. However, in order to do meaningful scRNA-seq analyses, all users will need to understand the implemented methods and their possible options and limitations.

scholarly journals BREC: an R package/Shiny app for automatically identifying heterochromatin boundaries and estimating local recombination rates along chromosomes

2021 ◽  
Vol 22 (S6) ◽  
Author(s):  
Yasmine Mansour ◽  
Annie Chateau ◽  
Anna-Sophie Fiston-Lavier
Keyword(s):  
Data Quality ◽  
Data Science ◽  
Fruit Fly ◽  
R Package ◽  
Model Organisms ◽  
Data Quality Control ◽  
Recombination Rates ◽  
Functional Dynamics ◽  
Shiny App ◽  
User Friendly

Abstract Background Meiotic recombination is a vital biological process playing an essential role in genome's structural and functional dynamics. Genomes exhibit highly various recombination profiles along chromosomes associated with several chromatin states. However, eu-heterochromatin boundaries are not available nor easily provided for non-model organisms, especially for newly sequenced ones. Hence, we miss accurate local recombination rates necessary to address evolutionary questions. Results Here, we propose an automated computational tool, based on the Marey maps method, allowing to identify heterochromatin boundaries along chromosomes and estimating local recombination rates. Our method, called BREC (heterochromatin Boundaries and RECombination rate estimates) is non-genome-specific, running even on non-model genomes as long as genetic and physical maps are available. BREC is based on pure statistics and is data-driven, implying that good input data quality remains a strong requirement. Therefore, a data pre-processing module (data quality control and cleaning) is provided. Experiments show that BREC handles different markers' density and distribution issues. Conclusions BREC's heterochromatin boundaries have been validated with cytological equivalents experimentally generated on the fruit fly Drosophila melanogaster genome, for which BREC returns congruent corresponding values. Also, BREC's recombination rates have been compared with previously reported estimates. Based on the promising results, we believe our tool has the potential to help bring data science into the service of genome biology and evolution. We introduce BREC within an R-package and a Shiny web-based user-friendly application yielding a fast, easy-to-use, and broadly accessible resource. The BREC R-package is available at the GitHub repository https://github.com/GenomeStructureOrganization.

scholarly journals Introducing bdclean: a user friendly biodiversity data cleaning pipeline

2018 ◽  
Vol 2 ◽  
pp. e25564
Author(s):  
Tomer Gueta ◽  
Vijay Barve ◽  
Thiloshon Nagarajah ◽  
Ashwin Agrawal ◽  
Yohay Carmel
Keyword(s):  
Data Cleaning ◽  
Control Process ◽  
R Package ◽  
Modular Approach ◽  
Data Validation ◽  
Biodiversity Data ◽  
Quality Control Process ◽  
Cleaning Procedures ◽  
R Packages ◽  
User Friendly

A new R package for biodiversity data cleaning, 'bdclean', was initiated in the Google Summer of Code (GSoC) 2017 and is available on github. Several R packages have great data validation and cleaning functions, but 'bdclean' provides features to manage a complete pipeline for biodiversity data cleaning; from data quality explorations, to cleaning procedures and reporting. Users are able go through the quality control process in a very structured, intuitive, and effective way. A modular approach to data cleaning functionality should make this package extensible for many biodiversity data cleaning needs. Under GSoC 2018, 'bdclean' will go through a comprehensive upgrade. New features will be highlighted in the demonstration.

scholarly journals FIREcaller: Detecting Frequently Interacting Regions from Hi-C Data

2019 ◽  
Author(s):  
Cheynna Crowley ◽  
Yuchen Yang ◽  
Yunjiang Qiu ◽  
Benxia Hu ◽  
Armen Abnousi ◽  
...  
Keyword(s):  
Gene Regulation ◽  
Spatial Organization ◽  
R Package ◽  
Specific Gene ◽  
List Type ◽  
Cell Type ◽  
R Software ◽  
Computational Tools ◽  
Cell Type Specific ◽  
User Friendly

AbstractHi-C experiments have been widely adopted to study chromatin spatial organization, which plays an essential role in genome function. We have recently identified frequently interacting regions (FIREs) and found that they are closely associated with cell-type-specific gene regulation. However, computational tools for detecting FIREs from Hi-C data are still lacking. In this work, we present FIREcaller, a stand-alone, user-friendly R package for detecting FIREs from Hi-C data. FIREcaller takes raw Hi-C contact matrices as input, performs within-sample and cross-sample normalization, and outputs continuous FIRE scores, dichotomous FIREs, and super-FIREs. Applying FIREcaller to Hi-C data from various human tissues, we demonstrate that FIREs and super-FIREs identified, in a tissue-specific manner, are closely related to gene regulation, are enriched for enhancer-promoter (E-P) interactions, tend to overlap with regions exhibiting epigenomic signatures of cis-regulatory roles, and aid the interpretation or GWAS variants. The FIREcaller package is implemented in R and freely available at https://yunliweb.its.unc.edu/FIREcaller.Highlights– Frequently Interacting Regions (FIREs) can be used to identify tissue and cell-type-specific cis-regulatory regions.– An R software, FIREcaller, has been developed to identify FIREs and clustered FIREs into super-FIREs.

scholarly journals ctmmweb: A graphical user interface for autocorrelation-informed home range estimation

2020 ◽  
Author(s):  
Justin M. Calabrese ◽  
Christen H. Fleming ◽  
Michael J. Noonan ◽  
Xianghui Dong
Keyword(s):  
Home Range ◽  
Kernel Density ◽  
R Package ◽  
Home Ranges ◽  
Tracking Data ◽  
Sampled Data ◽  
Convex Polygons ◽  
Range Estimation ◽  
Empirical Reality ◽  
Range Overlap

ABSTRACTEstimating animal home ranges is a primary purpose of collecting tracking data. All conventional home range estimators in widespread usage, including minimum convex polygons and kernel density estimators, assume independently sampled data. In stark contrast, modern GPS animal tracking datasets are almost always strongly autocorrelated. This incongruence between estimator assumptions and empirical reality leads to systematically underestimated home ranges. Autocorrelated kernel density estimation (AKDE) resolves this conflict by modeling the observed autocorrelation structure of tracking data during home range estimation, and has been shown to perform accurately across a broad range of tracking datasets. However, compared to conventional estimators, AKDE requires additional modeling steps and has heretofore only been accessible via the command-line ctmm R package. Here, we introduce ctmmweb, which provides a point-and-click graphical interface to ctmm, and streamlines AKDE, its prerequisite autocorrelation modeling steps, and a number of additional movement analyses. We demonstrate ctmmweb’s capabilities, including AKDE home range estimation and subsequent home range overlap analysis, on a dataset of four jaguars from the Brazilian Pantanal. We intend ctmmweb to open AKDE and related autocorrelation-explicit analyses to a wider audience of wildlife and conservation professionals.

PITR: A New Open Source R Package for PIT Telemetry Data

Fisheries ◽  
2018 ◽  
Vol 43 (1) ◽  
pp. 5-5 ◽  
Author(s):  
Joel M. S. Harding ◽  
Douglas C. Braun ◽  
Nicholas J. Burnett ◽  
Annika Putt
Keyword(s):  
Open Source ◽  
R Package ◽  
Telemetry Data ◽  
Pit Telemetry

Joint DNA-based Disaster Victim Identification

2021 ◽  
Author(s):  
Magnus Dehli Vigeland ◽  
Thore Egeland
Keyword(s):  
A Priori ◽  
Search Space ◽  
R Package ◽  
Individual Identification ◽  
Disaster Victim Identification ◽  
Data Set ◽  
Victim Identification ◽  
Joint Identification ◽  
Available Information ◽  
User Friendly

Abstract We address computational and statistical aspects of DNA-based identification of victims in the aftermath of disasters. Current methods and software for such identification typically consider each victim individually, leading to suboptimal power of identification and potential inconsistencies in the statistical summary of the evidence. We resolve these problems by performing joint identification of all victims, using the complete genetic data set. Individual identification probabilities, conditional on all available information, are derived from the joint solution in the form of posterior pairing probabilities. A closed formula is obtained for the a priori number of possible joint solutions to a given DVI problem. This number increases quickly with the number of victims and missing persons, posing computational challenges for brute force approaches. We address this complexity with a preparatory sequential step aiming to reduce the search space. The examples show that realistic cases are handled efficiently. User-friendly implementations of all methods are provided in the R package dvir, freely available on all platforms.

scholarly journals DiscoRhythm: an easy-to-use web application and R package for discovering rhythmicity

2019 ◽  
Author(s):  
Matthew Carlucci ◽  
Algimantas Kriščiūnas ◽  
Haohan Li ◽  
Povilas Gibas ◽  
Karolis Koncevičius ◽  
...  
Keyword(s):  
Web Application ◽  
Statistical Significance ◽  
R Package ◽  
Biological Data ◽  
Supplementary Information ◽  
Statistical Knowledge ◽  
Health And Disease ◽  
Phase Amplitude ◽  
Almost All ◽  
User Friendly

Abstract Motivation Biological rhythmicity is fundamental to almost all organisms on Earth and plays a key role in health and disease. Identification of oscillating signals could lead to novel biological insights, yet its investigation is impeded by the extensive computational and statistical knowledge required to perform such analysis. Results To address this issue, we present DiscoRhythm (Discovering Rhythmicity), a user-friendly application for characterizing rhythmicity in temporal biological data. DiscoRhythm is available as a web application or an R/Bioconductor package for estimating phase, amplitude, and statistical significance using four popular approaches to rhythm detection (Cosinor, JTK Cycle, ARSER, and Lomb-Scargle). We optimized these algorithms for speed, improving their execution times up to 30-fold to enable rapid analysis of -omic-scale datasets in real-time. Informative visualizations, interactive modules for quality control, dimensionality reduction, periodicity profiling, and incorporation of experimental replicates make DiscoRhythm a thorough toolkit for analyzing rhythmicity. Availability and Implementation The DiscoRhythm R package is available on Bioconductor (https://bioconductor.org/packages/DiscoRhythm), with source code available on GitHub (https://github.com/matthewcarlucci/DiscoRhythm) under a GPL-3 license. The web application is securely deployed over HTTPS (https://disco.camh.ca) and is freely available for use worldwide. Local instances of the DiscoRhythm web application can be created using the R package or by deploying the publicly available Docker container (https://hub.docker.com/r/mcarlucci/discorhythm). Supplementary information Supplementary data are available at Bioinformatics online.

scholarly journals NanoR: A user-friendly R package to analyze and compare nanopore sequencing data

PLoS ONE ◽  
2019 ◽  
Vol 14 (5) ◽  
pp. e0216471 ◽  
Author(s):  
Davide Bolognini ◽  
Niccolò Bartalucci ◽  
Alessandra Mingrino ◽  
Alessandro Maria Vannucchi ◽  
Alberto Magi
Keyword(s):  
R Package ◽  
Nanopore Sequencing ◽  
Sequencing Data ◽  
User Friendly

MetENP/MetENPWeb: An R package and web application for metabolomics enrichment and pathway analysis in Metabolomics Workbench

2020 ◽  
Author(s):  
Kumari Sonal Choudhary ◽  
Eoin Fahy ◽  
Kevin Coakley ◽  
Manish Sud ◽  
Mano R Maurya ◽  
...  
Keyword(s):  
Pathway Analysis ◽  
Web Application ◽  
Enrichment Analysis ◽  
R Package ◽  
Pathway Enrichment Analysis ◽  
Pathway Enrichment ◽  
Kegg Pathways ◽  
Link Type ◽  
Species Specific ◽  
User Friendly

ABSTRACTWith the advent of high throughput mass spectrometric methods, metabolomics has emerged as an essential area of research in biomedicine with the potential to provide deep biological insights into normal and diseased functions in physiology. However, to achieve the potential offered by metabolomics measures, there is a need for biologist-friendly integrative analysis tools that can transform data into mechanisms that relate to phenotypes. Here, we describe MetENP, an R package, and a user-friendly web application deployed at the Metabolomics Workbench site extending the metabolomics enrichment analysis to include species-specific pathway analysis, pathway enrichment scores, gene-enzyme information, and enzymatic activities of the significantly altered metabolites. MetENP provides a highly customizable workflow through various user-specified options and includes support for all metabolite species with available KEGG pathways. MetENPweb is a web application for calculating metabolite and pathway enrichment analysis.Availability and ImplementationThe MetENP package is freely available from Metabolomics Workbench GitHub: (https://github.com/metabolomicsworkbench/MetENP), the web application, is freely available at (https://www.metabolomicsworkbench.org/data/analyze.php)

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