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80 stars written in R
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Friends don't let friends make certain types of data visualization - What are they and why are they bad.

R 6,523 253 Updated Dec 10, 2024

simple tools for data cleaning in R

R 1,398 130 Updated Dec 23, 2024

Apply Mapping Functions in Parallel using Futures

R 704 40 Updated Dec 29, 2024

A grammar of graphics for comparative genomics

R 632 65 Updated Dec 5, 2024

A geom for ggplot to create bump plots

R 539 31 Updated Apr 3, 2024

ggplot2 extension for alluvial plots

R 503 34 Updated Dec 13, 2024

Summarize, Analyze and Visualize MAF files from TCGA or in-house studies.

R 452 223 Updated Nov 7, 2024

Interactive Heat Maps for R Using plotly

R 380 73 Updated Jul 16, 2024

Combination matrix axis for 'ggplot2' to create 'UpSet' plots

R 354 25 Updated Jun 24, 2024

Easy memoisation for R

R 318 56 Updated Dec 5, 2023

An R package to simulate colorblindness on R figures.

R 307 29 Updated Jul 17, 2023

Get You to Your Desired Plot Faster

R 290 35 Updated Nov 16, 2021

Manipulate CSV files on the command line using dplyr

R 270 20 Updated Feb 9, 2022

Multi-Omics Factor Analysis

R 233 60 Updated Sep 30, 2020

Quality control for MinION sequencing data

R 215 41 Updated Jan 26, 2023

🚀 R package: future.apply - Apply Function to Elements in Parallel using Futures

R 212 17 Updated Dec 28, 2024

R package for the joint analysis of multiple single-cell RNA-seq datasets

R 203 39 Updated Feb 26, 2024

Automated, probabilistic assignment of cell types in scRNA-seq data

R 199 83 Updated Jan 9, 2023

Dark mode for ggplot2 themes

R 197 9 Updated Oct 10, 2019

Interfaces for Multivariate Analysis in R

R 193 13 Updated Sep 28, 2023

3d extension to ggplot

R 186 5 Updated Dec 21, 2020

Simple statistical identification and removal of contaminants in marker-gene and metagenomics sequencing data

R 150 25 Updated Mar 22, 2023

🌲 An easy-to-use and scalable toolkit for genomic alteration signature (a.k.a. mutational signature) analysis and visualization in R https://shixiangwang.github.io/sigminer/reference/index.html

R 149 19 Updated Oct 12, 2024

Algorithm to implement Fraction and Copy number Estimate from Tumor/normal Sequencing.

R 146 67 Updated Jun 4, 2023

deconstructSigs

R 140 47 Updated Apr 24, 2023

Copy number calling and variant classification using targeted short read sequencing

R 130 32 Updated Jan 3, 2025

Reference-free profiling of polyploid genomes

R 110 18 Updated Jul 10, 2024

Analysis pipeline for cancer sequencing data

R 110 33 Updated Jul 3, 2024

Genome Interval Arithmetic in R

R 89 25 Updated Dec 27, 2024
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