Aim: This project aims to identify keystone species of the human gut microbiome, their functional niche and versatility.
Approach: We identify putative keystone species by analyzing publicly available metagenome and metatranscriptome datasets. Specifically, we assess topological features of correlation networks and functional profiles of microbial species in the human gut. We then use these characteristics to estimate each species potential for acting as a keystone species.
Student: Franziska Bauchinger
Faculty: David Berry (PI)
Funding: European Research Council