Cancer data analysis, NGS, epigenetics
Sebastian DiLorenzo has an MSc in Bioinformatics from Uppsala University and is located at the Biomedical Center in Uppsala. He primarily provides support on analysis and clinical use of data from cancer samples. Analyses include mutation analysis, allele-specific DNA copy number, DNA methylation and bioinformatics pipelines. As a previous SNIC application expert he has a good understanding of UPPMAX and general HPC environments. He participates in SciLifeLab hosted courses in Basic Bioinformatics and Computational Methods in Massively Parallel Sequencing where he occasionally lectures on allele-specific copy number analysis in cancer data.