Search for: All records

ategorizing individual cells into one of many known cell-type categories, also known as cell-type annotation, is a critical step in the analysis of single-cell genomics data. The current process of annotation is time intensive and subjective, which has led to different studies describing cell types with labels of varying degrees of resolution. While supervised learning approaches have provided automated solutions to annotation, there remains a significant challenge in fitting a unified model for multiple datasets with inconsistent labels. In this article we propose a new multinomial logistic regression estimator which can be used to model cell-type probabilities by integrating multiple datasets with labels of varying resolution. To compute our estimator, we solve a nonconvex optimization problem using a blockwise proximal gradient descent algorithm. We show through simulation studies that our approach estimates cell-type probabilities more accurately than competitors in a wide variety of scenarios. We apply our method to 10 single-cell RNA-seq datasets and demonstrate its utility in predicting fine resolution cell-type labels on unlabeled data as well as refining cell-type labels on data with existing coarse resolution annotations. Finally, we demonstrate that our method can lead to novel scientific insights in the context of a differential expression analysis comparing peripheral blood gene expression before and after treatment with interferon-β. An R package implementing the method is available in the Supplementary Material and at https://github.com/keshav-motwani/IBMR, and the collection of datasets we analyze is available at https://github.com/keshav-motwani/AnnotatedPBMC.