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Marchand-Maillet, S.

Publications and source records attributed to Marchand-Maillet, S..

2 recordsLinked to original sources

TimeFlow 2: an unsupervised cell lineage detection method for flow cytometry data

Cell lineage detection refers to the inference of differentiation pathways from immature cells to distinct mature cell types. We developed TimeFlow 2, a new method for lineage inference in large flow cytometry datasets. It uses a single static snapshot of unordered cells and does not require prior knowledge of the number of pathways, cell type or temporal labels. TimeFlow 2 uses the cell orderings from TimeFlow and defines coarse cell states along pseudotime segments. By connecting these states, it constructs paths at cell state level. To approximate the trajectory structure, it further groups the paths based on an Optimal Transport-based cost function. We used TimeFlow 2 on three healthy bone marrow samples and accurately assigned monocytes, neutrophils, erythrocytes and B-cells of different maturation stages to four distinct pathways. Marker dynamics across the inferred pathways showed highly correlated patterns for the corresponding lineages in all three patients. We compared the performance of TimeFlow 2 and three other established methods using standard classification and correlation metrics. TimeFlow 2 outperformed the others on flow cytometry datasets and remained competitive on the challenging mass cytometry datasets. Overall, TimeFlow 2 detects biologically informative pathways, allowing bioinformaticians to model and compare marker dynamics across cell lineages in a data-driven way. Source code in Python and tutorials are available at https://github.com/MargaritaLiarou1/TimeFlow2.

bioinformatics↗

TimeFlow: a density-driven pseudotime method for flowcytometry data analysis

Pseudotime methods order cells undergoing differentiation from the least to most differentiated. We developed TimeFlow, a new method for computing pseudotime in multi-dimensional flow cytometry datasets. TimeFlow tracks the differentiation path of each cell on a graph by following smooth changes in the cell population density. To compute the probability density function of the cells, it uses a normalizing flow model. We profiled bone marrow samples from three healthy patients using a 20-color antibody panel for flow cytometry and prepared datasets that ranged from 5,000 to 600,000 cells and included monocytes, neutrophils, erythrocytes and B-cells at various maturation stages. TimeFlow computed fine-grained pseudotime for all the datasets, and the cell orderings were consistent with prior knowledge of human hematopoiesis. Experiments showed its potential in generalizing across patients and unseen cell states. We compared our method to 11 other pseudotime methods using in-house and public datasets and found very good performance for both linear and branching trajectories. TimeFlows pseudotemporal orderings are useful for modelling the dynamics of cell surface proteins along linear trajectories. The biologically meaningful results in branching trajectories suggest the possibility of future applications with automated cell lineage detection. Code is available at https://github.com/MargaritaLiarou1/TimeFlow and bone marrow data will be accessible upon acceptance.

bioinformatics↗