RADseq Data Exploration, Manipulation and Visualization using R

Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata

The Visualization Multitool for Molecular Epidemiology and Bioinformatics

simple coverage distribution profile of aligned samples. useful for sequencing center feedback and topoffs.

Analysis of SNP variants, derived from chip array genotyping and HTS sequencing

Visualization recommender and UI for complex non-tabular data and linked static charts

UC Davis: Data Science for Biologists - R markdown

Frontend web application for wally to visualize aligned sequencing reads

Motif Visualisation and multi-omic integration tool

R-Shiny App displaying the GC Skew of bacterial genomes

DataViz 2.0 | Spring 2020 workshop

Host a UCSC trackhub on GitHub

learn R by rote

My personal website