Expertise in Python, particularly in using pandas data frames for data wrangling. Familiarity with standard bioinformatics NGS data formats and annotations. Proficiency in Unix/Linux environments and Bash scripting. Understanding of different assays and modes of sequencing (WGS vs. Exome, RNA-seq, Tumor vs. Normal, Somatic vs. Germline, etc.). Understanding of NGS biomarkers related to cancer (e.g. copy numbers, fusions, SNV and INDELs).