ahmetz/oncoprint
Create beautilful oncoprints in R
R package to generate onco prints of genomic and clinical data of patient cohorts
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Create beautilful oncoprints in R
Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms
iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Generation DNA sequencing data.
All graphs in “Creating More Effective Graphs”, made with R package ggplot2.