| Literature DB >> 30067990 |
Zicheng Hu1, Chethan Jujjavarapu1, Jacob J Hughey2, Sandra Andorf3, Hao-Chih Lee4, Pier Federico Gherardini5, Matthew H Spitzer6, Cristel G Thomas7, John Campbell7, Patrick Dunn7, Jeff Wiser7, Brian A Kidd4, Joel T Dudley4, Garry P Nolan8, Sanchita Bhattacharya1, Atul J Butte9.
Abstract
While meta-analysis has demonstrated increased statistical power and more robust estimations in studies, the application of this commonly accepted methodology to cytometry data has been challenging. Different cytometry studies often involve diverse sets of markers. Moreover, the detected values of the same marker are inconsistent between studies due to different experimental designs and cytometer configurations. As a result, the cell subsets identified by existing auto-gating methods cannot be directly compared across studies. We developed MetaCyto for automated meta-analysis of both flow and mass cytometry (CyTOF) data. By combining clustering methods with a silhouette scanning method, MetaCyto is able to identify commonly labeled cell subsets across studies, thus enabling meta-analysis. Applying MetaCyto across a set of ten heterogeneous cytometry studies totaling 2,926 samples enabled us to identify multiple cell populations exhibiting differences in abundance between demographic groups. Software is released to the public through Bioconductor (http://bioconductor.org/packages/release/bioc/html/MetaCyto.html).Entities:
Keywords: CyTOF; flow cytometry; human immunology; immune cells; meta-analysis
Mesh:
Year: 2018 PMID: 30067990 PMCID: PMC6583920 DOI: 10.1016/j.celrep.2018.07.003
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423