MetaCyto
MetaCyto performs automated meta-analysis of flow and mass cytometry (CyTOF) datasets to integrate heterogeneous studies and identify comparable cell subsets for cross-study comparison.
Key Features:
- Automated Meta-Analysis: Performs automated meta-analysis across heterogeneous cytometry studies despite varying marker sets and inconsistent marker values caused by different experimental designs and instrument configurations.
- Clustering and Silhouette Scanning Methodology: Combines clustering methods with silhouette scanning to identify cell subsets commonly labeled across multiple studies.
- Cross-Study Comparability: Enables direct comparison of cytometry data by identifying consistently labeled cell subsets across studies, addressing limitations of traditional auto-gating methods.
Scientific Applications:
- Meta-analysis of cytometry cohorts: Applied to ten heterogeneous cytometry studies comprising 2,926 samples to identify multiple cell populations with differing abundance between demographic groups.
Methodology:
MetaCyto integrates clustering methods with silhouette scanning to identify common cell subsets across studies and accommodate variability in marker usage and detection values.
Topics
Collections
Details
- License:
- GPL-2.0
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- R
- Added:
- 7/12/2018
- Last Updated:
- 11/24/2024
Operations
Data Inputs & Outputs
Publications
Hu Z, Jujjavarapu C, Hughey JJ, Andorf S, Lee H, Gherardini PF, Spitzer MH, Dunn P, Thomas CG, Campbell J, Wiser J, Kidd BA, Dudley JT, Nolan GP, Bhattacharya S, Butte AJ. Meta-analysis of Cytometry Data Reveals Racial Differences in Immune Cells. Unknown Journal. 2017. doi:10.1101/130948.
Hu Z, Jujjavarapu C, Hughey JJ, Andorf S, Lee H, Gherardini PF, Spitzer MH, Thomas CG, Campbell J, Dunn P, Wiser J, Kidd BA, Dudley JT, Nolan GP, Bhattacharya S, Butte AJ. MetaCyto: A Tool for Automated Meta-analysis of Mass and Flow Cytometry Data. Cell Reports. 2018;24(5):1377-1388. doi:10.1016/j.celrep.2018.07.003. PMID:30067990. PMCID:PMC6583920.