MSc or PhD in Bioinformatics, Computational Biology or related fields.
Solid knowledge of Python or R, and Unix shell.
Familiarity with high performance computing environments.
Familiarity with BWA, GATK and genetic variant annotation software (e.g. Annovar, VEP), in relation to whole exome and whole genome data analysis pipelines.
Good understanding of human genetics and interpretation of genetic variant data.
Elementary working knowledge of biostatistics.
At least 4 year post-graduate experience (academic or industrial).
