Vincent Cabeli

ORCID: 0000-0003-0818-2518
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About
Contact & Profiles
Research Areas
  • Cell Image Analysis Techniques
  • Advanced Fluorescence Microscopy Techniques
  • Bayesian Modeling and Causal Inference
  • Single-cell and spatial transcriptomics
  • Bioinformatics and Genomic Networks
  • Biomedical Text Mining and Ontologies
  • Cancer-related molecular mechanisms research
  • Hematopoietic Stem Cell Transplantation
  • Genomics and Phylogenetic Studies
  • Hippo pathway signaling and YAP/TAZ
  • Molecular Biology Techniques and Applications
  • Mesenchymal stem cell research
  • Neural Networks and Applications
  • Breast Cancer Treatment Studies
  • AI in cancer detection
  • Computational Drug Discovery Methods
  • Genetics, Bioinformatics, and Biomedical Research
  • Cardiovascular Effects of Exercise
  • Immune cells in cancer
  • AI-based Problem Solving and Planning
  • Machine Learning in Healthcare
  • Cancer Genomics and Diagnostics
  • Cancer Cells and Metastasis
  • Data Quality and Management
  • Opinion Dynamics and Social Influence

Sorbonne Université
2020-2025

Université Paris Sciences et Lettres
2019-2025

Institut Curie
2019-2025

Centre National de la Recherche Scientifique
2020-2025

Daikin (United States)
2024

Physique des Cellules et Cancers
2019-2020

Institut de Mathématiques de Jussieu-Paris Rive Gauche
2020

Université Paris Cité
2018

We present PyDESeq2, a python implementation of the DESeq2 workflow for differential expression analysis on bulk RNA-seq data. This re-implementation yields similar, but not identical, results: it achieves higher model likelihood, allows speed improvements large datasets, as shown in experiments TCGA data, and can be more easily interfaced with modern python-based data science tools.PyDESeq2 is released an open-source software under MIT license. The source code available GitHub at...

10.1093/bioinformatics/btad547 article EN cc-by Bioinformatics 2023-09-01

Discovering causal effects is at the core of scientific investigation but remains challenging when only observational data are available. In practice, networks difficult to learn and interpret, limited relatively small datasets. We report a more reliable scalable discovery method (iMIIC), based on general mutual information supremum principle, which greatly improves precision inferred relations while distinguishing genuine causes from putative latent effects. showcase iMIIC synthetic...

10.1016/j.isci.2024.109736 article EN cc-by iScience 2024-04-16

Abstract Summary We present PyDESeq2, a python implementation of the DESeq2 workflow for differential expression analysis on bulk RNA-seq data. This achieves better precision, allows speed improvements large datasets, as shown in experiments TCGA data, and can be more easily interfaced with modern python-based data science tools. Availability Implementation PyDESeq2 is released an open-source software under MIT license. The source code available GitHub at https://github.com/owkin/PyDESeq2 ....

10.1101/2022.12.14.520412 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-12-16

Live-cell microscopy routinely provides massive amounts of time-lapse images complex cellular systems under various physiological or therapeutic conditions. However, this wealth data remains difficult to interpret in terms causal effects. Here, we describe CausalXtract, a flexible computational pipeline that discovers and possibly time-lagged effects from morphodynamic features cell–cell interactions live-cell imaging data. CausalXtract methodology combines network-based information-based...

10.7554/elife.95485.3 article EN cc-by eLife 2025-01-17

The precise diagnostics of complex diseases require to integrate a large amount information from heterogeneous clinical and biomedical data, whose direct indirect interdependences are notoriously difficult assess. To this end, we propose an efficient computational approach simultaneously compute assess the significance multivariate between any combination mixed-type (continuous/categorical) variables. method is then used uncover direct, possibly causal relationships data medical records, by...

10.1371/journal.pcbi.1007866 article EN cc-by PLoS Computational Biology 2020-05-18

The cardinal property of bone marrow (BM) stromal cells is their capacity to contribute hematopoietic stem cell (HSC) niches by providing mediators assisting HSC functions. In this study we first contrasted transcriptomes at different developmental stages and then included large number HSC-supportive non-supportive samples. Application a combination algorithms, comprising one identifying reliable paths potential causative relationships in complex systems, revealed gene networks...

10.1016/j.isci.2020.101222 article EN cc-by-nc-nd iScience 2020-05-30

Despite unprecedented amount of information now available in medical records, health data remain underexploited due to their heterogeneity and complexity. Simple charts hypothesis-driven statistics can no longer apprehend the content information-rich clinical data. There is, therefore, a clear need for powerful interactive visualization tools enabling practitioners perceive patterns insights gained by state-of-the-art machine learning algorithms. Here, we report an graphical interface use as...

10.1038/s41746-022-00647-0 article EN cc-by npj Digital Medicine 2022-08-10

SUMMARY Following infection, hematopoietic stem and progenitor cells (HSPCs) support immunity by increasing the rate of innate immune cell production but metabolic cues that guide this process are unknown. To address question, we developed MetaFate, a method to trace expression state developmental fate single in vivo . Using MetaFate identified gene program enzymes transporters confers differences myeloid differentiation potential subset HSPCs express CD62L. single-cell profiling, confirmed...

10.1101/2023.01.24.525166 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-01-24

Abstract Deep learning (DL) has shown potential to provide powerful representations of bulk RNA-seq data in cancer research. However, there is no consensus regarding the impact design choices DL approaches on performance learned representation, including model architecture, training methodology and various hyperparameters. To address this problem, we evaluate representation methods using TCGA DepMap pan-cancer datasets, assess their predictive power for survival gene essentiality...

10.1101/2024.01.23.576852 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-01-26

Deep learning (DL) has shown potential to provide powerful representations of bulk RNA-seq data in cancer research. However, there is no consensus regarding the impact design choices DL approaches on performance learned representation, including model architecture, training methodology and various hyperparameters. To address this problem, we evaluate representation methods using TCGA DepMap pan-cancer datasets assess their predictive power for survival gene essentiality predictions. We...

10.1038/s41598-024-67023-8 article EN cc-by-nc-nd Scientific Reports 2024-07-24

Live-cell microscopy routinely provides massive amounts of time-lapse images complex cellular systems under various physiological or therapeutic conditions. However, this wealth data remains difficult to interpret in terms causal effects. Here, we describe CausalXtract, a flexible computational pipeline that discovers and possibly time-lagged effects from morphodynamic features cell–cell interactions live-cell imaging data. CausalXtract methodology combines network-based information-based...

10.7554/elife.95485 article EN cc-by eLife 2024-09-17

Live-cell microscopy routinely provides massive amount of time-lapse images complex cellular systems under various physiological or therapeutic conditions. However, this wealth data remains difficult to interpret in terms causal effects. Here, we describe CausalXtract, a flexible computational pipeline that discovers and possibly time-lagged effects from morphodynamic features cell-cell interactions live-cell imaging data. CausalXtract methodology combines network-based information-based...

10.7554/elife.95485.1 preprint EN 2024-09-17

Discovering causal effects is at the core of scientific investigation but remains challenging when only observational data available. In practice, networks are difficult to learn and interpret, limited relatively small datasets. We report a more reliable scalable discovery method (iMIIC), based on general mutual information supremum principle, which greatly improves precision inferred relations while distinguishing genuine causes from putative latent effects. showcase iMIIC synthetic...

10.48550/arxiv.2303.06423 preprint EN cc-by-nc-nd arXiv (Cornell University) 2023-01-01

Abstract Live-cell microscopy routinely provides massive amount of time-lapse images complex cellular systems under various physiological or therapeutic conditions. However, this wealth data remains difficult to interpret in terms causal effects. Here, we describe CausalXtract, a flexible computational pipeline that discovers and possibly time-lagged effects from morphodynamic features cell-cell interactions live-cell imaging data. CausalXtract methodology combines network-based...

10.1101/2024.02.06.579177 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2024-02-08

Abstract Hippo signaling emerged over the last decade as a major tumor-suppressing pathway. Its dysregulation is generally associated with abnormal expression levels of YAP1, WWTR1 (coding for TAZ protein) and TEAD genes among others. This pathway has been shown to have prognostic impact in several cancer types. In particular, role YAP1/TEAD activity across indications emphasized by recent works, potential implications on treatment options. Therefore, identifying patients deregulated key...

10.1158/1538-7445.am2024-7377 article EN Cancer Research 2024-03-22

Summary Over the last decade, Hippo signaling has emerged as a major tumor-suppressing pathway. Its dysregulation is associated with abnormal expression of YAP1 and TEAD -family genes. Recent works have highlighted role YAP1/TEAD activity in several cancers its potential therapeutic implications. Therefore, identifying patients dysregulated pathway key to enhancing treatment impact. Although recent studies derived RNAseq-based signatures, there remains need for reproducible cost-effective...

10.1101/2024.06.14.598991 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-06-14

Live-cell microscopy routinely provides massive amount of time-lapse images complex cellular systems under various physiological or therapeutic conditions. However, this wealth data remains difficult to interpret in terms causal effects. Here, we describe CausalXtract, a flexible computational pipeline that discovers and possibly time-lagged effects from morphodynamic features cell-cell interactions live-cell imaging data. CausalXtract methodology combines network-based information-based...

10.7554/elife.95485.2 preprint EN 2024-12-06

The cardinal property of bone marrow (BM) stromal cells is their capacity to contribute Hematopoietic Stem Cell (HSC) niches by providing mediators assisting HSC functions. In this study we first contrasted transcriptomes at different developmental stages and then included large number HSC-supportive non-supportive samples. Application a combination algorithms enabled identifying gene network characteristic the BM defining niche populations perivascular cells, osteoblasts mesenchymal cells....

10.2139/ssrn.3498575 article EN SSRN Electronic Journal 2019-01-01
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