Resolving heterogeneity in Lymph Node Stromal Cells using high-dimensional analysis of non-optimized flow cytometry data

. However, LNSCs are challenging to work with due to their high heterogeneity. Here, we demonstrate the challenges of working with heterogeneous cell populations, where ratios between populations can change over time. We show how similar marker expression profiles between populations, along with non-optimized controls due to experimental limitations, can make flow cytometry analysis difficult. To better assess this heterogeneous population, we demonstrate how to use machine learning algorithms to identify changing populations while overcoming the limitations of any single algorithm. This approach reduces the effects of user bias when placing gates while also increasing confidence in population identification. This analysis method is robust, utilizes existing tools, and provides information that can inform various directions of future studies.