Cancer data analysis, NGS, epigenetics, Pipelines
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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 for cancer samples. His experiences include single-nucleotide and structural variant calling, epigenetics from bisulfite sequenced samples and method development for bioinformatics pipelines. As a former SNIC application expert he has a good understanding of UPPMAX and general HPC environments. He participates in SciLifeLab hosted courses such as “Introduction to Bioinformatics using NGS data”.