Anne Hartebrodt
Dr. Anne Hartebrodt
- Since March 2023 : Postdoctoral resesearcher at the Biomedical Network Science Lab, Department Artificial Intelligence in Biomedical Engineering, Friedrich-Alexander University Erlangen-Nürnberg, Erlangen, Germany. Studying Network based embeddings and carbon-aware computing for bioinformatics
- March 2022 – February 2023: Research assistant at University of Southern Denmark and Odense University Hospital (OUH)
- February 2019 – February 2022: PhD in Bioinformatics at University of Southern Denmark (SDU), Odense, Denmark. Thesis entitled Federated Unsupervised Machine Learning.
- October 2016 – December 2018 : Master in Bioinformatics at Technical University Munich (TUM) and Ludwig Maximilian University (LMU) Munich
- October 2012 – October 2016 : Bachelor in Bioinformatics at Technical University Munich (TUM) and Ludwig Maximilian University (LMU) Munich
2024
Decoil: Reconstructing Extrachromosomal DNA Structural Heterogeneity from Long-Read Sequencing Data
28th International Conference on Research in Computational Molecular Biology, RECOMB 2024 (Cambridge, MA, 29/04/2024 - 02/05/2024)
In: Jian Ma (ed.): Research in Computational Molecular Biology. 28th Annual International Conference, RECOMB 2024, Cambridge, MA, USA, April 29–May 2, 2024, Proceedings, Cham: 2024
DOI: 10.1007/978-1-0716-3989-4_41
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Federated singular value decomposition for high-dimensional data
In: Data Mining and Knowledge Discovery 38 (2024), p. 938 - 975
ISSN: 1573-756X
DOI: 10.1007/s10618-023-00983-z
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ZEB1-mediated fibroblast polarization controls inflammation and sensitivity to immunotherapy in colorectal cancer
In: EMBO Reports (2024)
ISSN: 1469-221X
DOI: 10.1038/s44319-024-00186-7
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Spatial cell graph analysis reveals skin tissue organization characteristic for cutaneous T cell lymphoma
In: npj Systems Biology and Applications 10 (2024), Article No.: 143
ISSN: 2056-7189
DOI: 10.1038/s41540-024-00474-x
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2023
Privacy of Federated QR Decomposition Using Additive Secure Multiparty Computation
In: IEEE Transactions on Information Forensics and Security 18 (2023), p. 5122-5132
ISSN: 1556-6013
DOI: 10.1109/TIFS.2023.3301710
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2022
Federated horizontally partitioned principal component analysis for biomedical applications
In: Bioinformatics Advances 2 (2022), Article No.: vbac026
ISSN: 2635-0041
DOI: 10.1093/bioadv/vbac026
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2021
Federated Principal Component Analysis for Genome-Wide Association Studies
21st IEEE International Conference on Data Mining (ICDM) (Auckland, New Zealand, 07/12/2021 - 10/12/2021)
In: 21st IEEE International Conference on Data Mining (ICDM) 2021
DOI: 10.1109/ICDM51629.2021.00127
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2023
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Dimensionality reduction for molecular data based on explanatory power of differential regulatory networks
(Third Party Funds Group – Overall project)
Term: 01/03/2023 - 28/02/2026
Funding source: Bundesministerium für Bildung und Forschung (BMBF)
URL: https://www.netmap.ai/Rapid advances in single-cell RNA sequencing (scRNA-seq) technology are leading to ever-increasing dimensions of the generated molecular data, which complicates data analyses. In NetMap, new scalable and robust dimensionality reduction approaches for scRNA-seq data will be developed. To this end, dimensionality reduction will be integrated into a central task of the systems medicine analysis of scRNA-seq data: inference of gene regulatory networks (GRNs) and driver transcription factors based on cell expression profiles. Each resulting dimension will correspond to a driver GRN, and the coordinate of a cell in this low-dimensional representation will quantify the extent to which the particular driver GRN explains the cell's gene expression profile. These new methods will be implemented as a user-friendly software platform for exploratory expert-in-the-loop analysis and in silico prediction of drug repurposing candidates.
As a case study, we will investigate CD4 helper T cell exhaustion, a potential limiting factor in immunotherapy. NetMap's strategy consists of (1) analyzing phenotypic heterogeneity of depleted CD4 T cells, (2) identifying transcriptional mechanisms that control this heterogeneity, (3) amplifying/eliminating specific subsets and testing their functional impact. This will allow the development of an atlas of the gene regulatory landscape of depleted CD4 T cells, while the in vivo testing of key regulatory transcription factors will help demonstrate the power of the developed methods and allow evaluation and improvement of predictions.