About our team
We study mutational processes and mechanisms of genome instability driving tumourigenesis, immune evasion, and drug response through high-throughput sequencing data from clinical samples.
Our group develops novel approaches for early cancer detection using long-read sequencing.
We invite applications for a Postdoctoral Fellow position in early detection, cancer genomics, and long-read sequencing data analysis.
Lead scalable and innovative computational solutions for sequencing data analysis.
Develop methods for analysing hundreds of long-read whole-genome sequencing data sets from human tumours and cell-free DNA samples.
This role requires PhD degree in life sciences, strong analytical skills, experience in computational genomics, Unix-based environments, high-performance computing, and reproducible data analysis pipelines.