An R package for detecting cell-to-cell variably methylated regions (VMRs) from single-cell bisulfite sequencing leveraging probabilistic models.

Epigenomics workflow system for the semi-automated analysis of NGS data

Project based on bash, python and R that contains all the tasks entrusted on the Epigenomics subject. All the instructions can be found on the "Wiki" access, as well as in the README.txt file.