TY - JOUR
T1 - Multibatch Cytometry Data Integration for Optimal Immunophenotyping
AU - Ogishi, Masato
AU - Yang, Rui
AU - Gruber, Conor
AU - Zhang, Peng
AU - Pelham, Simon J
AU - Spaan, András N
AU - Rosain, Jérémie
AU - Chbihi, Marwa
AU - Han, Ji Eun
AU - Rao, V Koneti
AU - Kainulainen, Leena
AU - Bustamante, Jacinta
AU - Boisson, Bertrand
AU - Bogunovic, Dusan
AU - Boisson-Dupuis, Stéphanie
AU - Casanova, Jean-Laurent
N1 - Publisher Copyright:
Copyright © 2020 by The American Association of Immunologists, Inc.
PY - 2021/1/1
Y1 - 2021/1/1
N2 - 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).
AB - 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).
KW - Algorithms
KW - Computational Biology
KW - Flow Cytometry
KW - Humans
KW - Immunophenotyping/methods
KW - Leukocytes, Mononuclear/physiology
KW - Software
UR - http://www.scopus.com/inward/record.url?scp=85097887715&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.2000854
DO - 10.4049/jimmunol.2000854
M3 - Article
C2 - 33229441
SN - 0022-1767
VL - 206
SP - 206
EP - 213
JO - Journal of immunology (Baltimore, Md. : 1950)
JF - Journal of immunology (Baltimore, Md. : 1950)
IS - 1
ER -