This study focuses on identifying immune, inflammatory, metabolic, and epigenetic drivers of post-infectious morbidity and mortality. It will evaluate how bacterial, viral, and TB pneumonia induce inflammation, metabolic perturbations, and epigenetic scars, leading to post-infectious morbidity and mortality. Single-cell technology will be implemented to identify drivers of post-infectious inflammation.
The successful candidate will receive training in analyses of single-cell and bulk-tissue multi-omics data and be expected to participate in multiple projects involving design, implementation, and integration of large-scale datasets and data processing pipelines
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