| Literature DB >> 33229441 |
Masato Ogishi1, Rui Yang2, Conor Gruber3,4,5,6, Peng Zhang2, Simon J Pelham2, András N Spaan2, Jérémie Rosain7,8, Marwa Chbihi2, Ji Eun Han2, V Koneti Rao9, Leena Kainulainen10,11, Jacinta Bustamante2,7,8,12, Bertrand Boisson2,7,8, Dusan Bogunovic3,4,5,6, Stéphanie Boisson-Dupuis2,7,8, Jean-Laurent Casanova2,7,8,13,14.
Abstract
High-dimensional cytometry is a powerful technique for deciphering the immunopathological factors common to multiple individuals. However, rational comparisons of multiple batches of experiments performed on different occasions or at different sites are challenging because of batch effects. In this study, we describe the integration of multibatch cytometry datasets (iMUBAC), a flexible, scalable, and robust computational framework for unsupervised cell-type identification across multiple batches of high-dimensional cytometry datasets, even without technical replicates. After overlaying cells from multiple healthy controls across batches, iMUBAC learns batch-specific cell-type classification boundaries and identifies aberrant immunophenotypes in patient samples from multiple batches in a unified manner. We illustrate unbiased and streamlined immunophenotyping using both public and in-house mass cytometry and spectral flow cytometry datasets. The method is available as the R package iMUBAC (https://github.com/casanova-lab/iMUBAC).Entities:
Mesh:
Year: 2020 PMID: 33229441 PMCID: PMC7855665 DOI: 10.4049/jimmunol.2000854
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422