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ter Huurne, M.

Publications and source records attributed to ter Huurne, M..

2 recordsLinked to original sources

FlowWeb, a free, web-based platform for flow cytometry data analysis

Flow cytometry is widely used for high-throughput single-cell analysis. However, its data analysis relies on either costly commercial software or programming-intensive open-source tools. To bridge this gap, we developed FlowWeb, a freely accessible, web-based platform that combines the flexibility of the R/Bioconductor ecosystem with an intuitive graphical user interface. FlowWeb enables integrated workflows for data handling, quality control, gating, visualization and statistical analysis within a unified environment. FlowWeb integrates raw data, metadata, and analytical state within synchronized Bioconductor structures, enabling coherent analysis and visualization workflows. FlowWeb supports both manual and automated data-driven gating workflows. To evaluate its performance, we applied FlowWeb to an in-house flow cytometry dataset and compared its automated cell cycle and gating workflows to established commercial tools. FlowWebs automated cell cycle workflow produced consistent and reproducible results across replicates and demonstrated high concordance with reference analyses, highlighting the platforms robustness. FlowWebs advanced visualization tools include a wide range of fully customizable individual, overlay, and statistical plots. To enhance usability and reproducibility, the FlowWeb platform provides optional user-accounts that allow storage of reusable configurations, including quality control presets, gating definitions, and plot templates. By lowering technical barriers without compromising analytical rigor, FlowWeb facilitates accessible, reproducible, and scalable flow cytometry data analysis for a broad range of users in research and clinical settings.

cell biology↗

Critical role for P53 in regulating the cell cycle of ground state embryonic stem cells

Mouse Embryonic Stem Cells (ESCs) grown in serum-supplemented conditions are characterized by an extremely short G1-phase due to the lack of G1-phase control. Concordantly, the G1-phase-specific P53-P21 pathway is compromised in serum ESCs. Here we provide evidence that P53 is activated upon transition of serum ESCs to their pluripotent ground state using serum-free 2i conditions and modulates G1-phase progression. Our data shows that the elongated G1-phase characteristic of ground state ESCs is dependent on P53. RNA-seq and ChIP-seq analyses reveal that P53 directly regulates the expression of the Retinoblastoma (RB) protein and that the hypo-phosphorylated, active RB protein plays a key role in G1-phase control. Our findings suggest that the P53-P21 pathway is active in ground state 2i ESCs and that its role in the G1-checkpoint is abolished in serum ESCs. Taken together, the data reveals a mechanism by which inactivation of P53 can lead to loss of RB and uncontrolled cell proliferation.

molecular biology↗