Focus on decoding the causal rules of life by interpretable AI models from multi-omic perturbation data to predict how complex tissues respond to disease and therapy.
We live in an era of exploding biological data.
We can now sequence genomes, profile single cells, and map entire tissues with extraordinary precision—giving us a detailed “parts list” of life itself.
But here’s the challenge: seeing the parts is not the same as understanding the system. Despite all this data, biology still lacks the ability to predict how complex systems behave. We know the components, but the blueprint remains hidden.
The next frontier in biology is clear: 👉 move from static maps to dynamic models that can learn, forecast, and explain life’s processes. This means shifting from correlation to causality, description to prediction.
Explore how Johnson’s research program is tackling this challenge— while also sharing insights into the cutting-edge biotechnologies shaping tomorrow’s breakthroughs.
I am a computational systems biologist dedicated to building predictive models of life. I believe that the next era of biological discovery and therapeutic design will be driven by our ability to learn the causal rules that govern complex cellular systems.
My scientific blueprint is to build interpretable AI models from a synthesis of multi-modal data, from single-cell genomics to spatial proteomics. By focusing on perturbation-response experiments, my work moves beyond correlation to infer the causal logic of how cellular networks operate and adapt.
PhD Biochemistry, 2016-2021
University of Regina, Canada
MSc Bioinformatics, 2009-2010
Univeristy of Manchester, England
BSc Biotechnology, 2004-2008
Nanjing Agricultural University, P.R. China