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41 stars written in R
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Easy interactive web applications with R

R 5,309 1,871 Updated Jun 13, 2024

dplyr: A grammar of data manipulation

R 4,698 2,116 Updated Jun 30, 2024

🎓 A collection of interactive courses for the swirl R package.

R 4,259 7,246 Updated Jan 10, 2024

Code accompanying the book "Machine Learning for Hackers"

R 3,662 2,216 Updated May 26, 2019

An interactive graphing library for R

R 2,522 621 Updated Jun 7, 2024

RStudio add-in to make plots interactively with ggplot2

R 1,757 227 Updated Jul 5, 2024

Simple web scraping for R

R 1,485 341 Updated Feb 26, 2024

Circular visualization in R

R 953 141 Updated Nov 11, 2023

Interactive grammar of graphics for R

R 715 174 Updated Feb 9, 2024

A template utility for R projects that provides a skeletal project.

R 623 159 Updated Jul 1, 2024

Creates Page Layout Visualizations in R 📄📄📄

R 331 12 Updated Jun 13, 2019

karyoploteR - An R/Bioconductor package to plot arbitrary data along the genome

R 293 42 Updated Jan 11, 2024

CanvasXpress: A JavaScript Library for Data Analytics with Full Audit Trail Capabilities.

R 287 44 Updated Jun 28, 2024

Quick mining and visualization of NGS data by integrating genomic databases

R 251 64 Updated May 5, 2023

Personal Cancer Genome Reporter (PCGR)

R 247 47 Updated Jul 5, 2024

Grid and ggplot2 based visualization for biological data

R 110 24 Updated Oct 30, 2023

Analysis pipeline for cancer sequencing data

R 107 33 Updated Jul 3, 2024

R client for Redis

R 93 25 Updated Jan 3, 2022

R package for genomic feature analysis and visualization

R 71 22 Updated Mar 6, 2020

Nozzle is a report generation toolkit for data analysis pipelines implemented in R.

R 68 22 Updated Apr 2, 2016

An R client for broads firehose pipeline, providing TCGA data sets

R 60 30 Updated Jun 25, 2019

a Shiny/R application to view and annotate copy number variations

R 26 12 Updated Mar 8, 2023

ONCOCNV - a package to detect copy number changes in Targeted Deep Sequencing and Exome-seq data

R 23 12 Updated Nov 2, 2022

create word cloud using the abstract from PubMed

R 22 7 Updated Feb 28, 2019

VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number variants (CNVs) from targeted next-generation sequencing data.…

R 22 12 Updated Dec 13, 2019

An online pedigree tool for research applications. Build pedigrees interactively and store as images or text files in ped format. QuickPed also computes a variety of relatedness coefficients and of…

R 20 3 Updated May 10, 2024

Easy Copy Number !

R 20 14 Updated Oct 18, 2021

Composable Functional Programming in R

R 16 3 Updated Jul 26, 2020

NExt generation Analysis Toolbox

R 13 7 Updated Oct 18, 2015
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