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Moritz Gerstung

@moritzgerstung.bsky.social
2.7K followers 413 following 23 posts

Scientist developing AI for oncology. Division head at the German Cancer Research Centre DKFZ. Prof at the University of Heidelberg, Germany. Previously at EMBL-EBI and Wellcome Sanger Institute. Alumnus of ETH Zurich.

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Reposted by Moritz Gerstung
Deutsches Krebsforschungszentrum (DKFZ) @dkfz.bsky.social · 18/03/2026
Do you want to do your #postdoc in #cancerresearch with the most prestigious fellowship in Europe? Apply to DKFZ #MSCA MasterClasses by May 18. 26 Projects in cancer research including #cellandmolecularbiology #genomics #bioinformatics #immunology. @horizoneu.bsky.social 👉Apply here: t1p.de/nx6tu
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Reposted by Moritz Gerstung
zaira seferbekova 👾 @zaira-sef.bsky.social · 06/10/2025
🚨 new glioblastoma preprint alert! we present the first spatially resolved single cell atlas comparing radionecrotic changes (RN) and recurrent IDH-wildtype glioblastoma (GB) –– shedding light on a long-standing diagnostic challenge. 🧵 1/
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Moritz Gerstung @moritzgerstung.bsky.social · 28/11/2025
Join us: With @abigailsuwala.bsky.social we are looking for a postdoc to drive our spatial transcriptomics analysis efforts of brain tumours. If you enjoy multidisciplinary biomedical research, big data and coding, you are in the right place. karriere.klinikum.uni-heidelberg.de/index.php?ac...
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Moritz Gerstung @moritzgerstung.bsky.social · 07/10/2025
A spatial transcriptomics analysis led by my student Zaira reveals the distinct nature (gene expression, tumour cell states and local microenvironments) of radionecrosis and recurrence in glioblastoma. 👏
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Reposted by Moritz Gerstung
Deutsches Krebsforschungszentrum (DKFZ) @dkfz.bsky.social · 18/09/2025
Scientists from @embl.org and DKFZ have developed an AI model that assesses the long-term individual risk for more than 1,000 diseases. The model can predict health events over a period of more than a decade. @moritzgerstung.bsky.social @nature.com t1p.de/zmjfg
t1p.de
AI model predicts disease risks decades in advance
Scientists from the European Molecular Biology Laboratory (EMBL) and the German Cancer Research Center (DKFZ) have developed an AI model that assesses the long-term individual risk for more than 1,000...
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Reposted by Moritz Gerstung
EMBL-EBI @ebi.embl.org · 17/09/2025
What if you could get a glimpse of the future of your health, today? Our scientists have developed a new generative AI model, trained using large-scale health records, that can estimate how human health may change over time. Watch to find out more. 🖥️🧬
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Moritz Gerstung @moritzgerstung.bsky.social · 29/07/2025
This is a great set of methods for studying combinatorial effects of cancer mutations on spatial phenotypes. Clever experimental design by @breinigmarco.bsky.social hijacking Visium and elegant analysis by @lomakinai.bsky.social and @elihei.bsky.social www.nature.com/articles/s41...
nature.com
Integrated in vivo combinatorial functional genomics and spatial transcriptomics of tumours to decode genotype-to-phenotype relationships - Nature Biomedical Engineering
A method integrates perturbation mapping with 10X Visium spatial transcriptomics to map tumour genetic complexity and heterogeneity.
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Omer Ali Bayraktar @bayraktarlab.bsky.social · 16/05/2025
How does tumour heterogeneity arise? How can we predict cancer cell plasticity? In 2 new studies, we trace #glioblastoma heterogeneity to a spatial cancer cell trajectory w. multimodal cell atlassing bit.ly/4mkrWgs & predict plasticity w. snRNA/ATAC+deep learning bit.ly/3FbI6Ic 🧵
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Nature Reviews Genetics @natrevgenet.nature.com · 29/04/2025
Spatial biology of cancer evolution go.nature.com/44hbib6 #Review by Zaira Seferbekova, @lomakinai.bsky.social, Lucy R. Yates & @moritzgerstung.bsky.social Free to read here: rdcu.be/c1jwe
go.nature.com
Spatial biology of cancer evolution - Nature Reviews Genetics
In this Review, the authors discuss our latest understanding of the spatial aspects of cancer evolution, including the roles of cancer subclonal structure, tissue architecture, and interactions betwee...
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Moritz Gerstung @moritzgerstung.bsky.social · 26/03/2025
Our experience with the multimodal seg is similar as yours- works great for many cell types or tissues, but not all. Plus there can be contaminating transcripts on top.
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Moritz Gerstung @moritzgerstung.bsky.social · 26/03/2025
Thank you! Yes, we believe segger has an edge over membrane-based segmentation because it also recognises the co-occurrence of transcripts. You can also use 10x multi-modal instead of nuclear segmentation as seggers input.
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Moritz Gerstung @moritzgerstung.bsky.social · 20/03/2025
and also myeloproliferative neoplasms. Back then, the implementation was very clunky and could only be done by R experts. ebmstate now makes the inference much easier with only a few lines of code. www.nejm.org/doi/full/10....
nejm.org
Classification and Personalized Prognosis in Myeloproliferative Neoplasms | NEJM
Myeloproliferative neoplasms, such as polycythemia vera, essential thrombocythemia, and myelofibrosis, are chronic hematologic cancers with varied progression rates. The genomic characterization of...
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Moritz Gerstung @moritzgerstung.bsky.social · 20/03/2025
This type of model predicts a patient’s journey across several mid- and endpoints and relates the progression to hundreds of variables. It was used to learn detailed prognostic models for acute myeloid leukaemia .. www.nature.com/articles/ng....
nature.com
Precision oncology for acute myeloid leukemia using a knowledge bank approach - Nature Genetics
Peter Campbell, Hartmut Döhner and colleagues present an analysis of genetic mutations and clinical information from 1,540 patients with acute myeloid leukemia, demonstrating the utility of clinical k...
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Moritz Gerstung @moritzgerstung.bsky.social · 20/03/2025
Some classical statistics today. ebmstate, an R package for multistate models with empirical Bayes covariate effect estimation. Developed by Rui Costa during his postdoc in my group. doi.org/10.32614/RJ-...
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Reposted by Moritz Gerstung
danapeer.bsky.social @danapeer.bsky.social · 20/03/2025
From great collaborations come great things. Excited to share Segger, the solution to segmentation of spatial transcriptomics (ST) data, with the @steglelab.bsky.social and @moritzgerstung.bsky.social labs, spearheaded by the great Andrew Moorman and Elyas Heidari www.biorxiv.org/content/10.1...
biorxiv.org
Segger: Fast and accurate cell segmentation of imaging-based spatial transcriptomics data
The accurate assignment of transcripts to their cells of origin remains the Achilles heel of imaging-based spatial transcriptomics, despite being critical for nearly all downstream analyses. Current c...
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Reposted by Moritz Gerstung
Stegle Lab @steglelab.bsky.social · 18/03/2025
1/ New preprint! 🍳 @elihei.bsky.social and our team at @embl.org , @dkfz.bsky.social, and @mskcancercenter.bsky.social built #segger - a fast, accurate cell segmentation tool for spatial transcriptomics that assigns transcripts to their cell origins! doi.org/10.1101/2025...
Segger logoMessage passing intuition behind the segger’s link-prediction model and the network architecture
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Moritz Gerstung @moritzgerstung.bsky.social · 18/03/2025
Also tagging Elyas Heidari @elihei.bsky.social here who led this fantastic work.
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Moritz Gerstung @moritzgerstung.bsky.social · 17/03/2025
A great thanks goes to all the other authors and contributors from the Gerstung, Stegle and Peer labs who made this work possible.
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Moritz Gerstung @moritzgerstung.bsky.social · 17/03/2025
Segger comes as robust open-source software and has already been tested by many in the community. github.com/EliHei2/segg...
github.com
GitHub - EliHei2/segger_dev: a cutting-edge cell segmentation model specifically designed for single-molecule resolved spatial omics datasets. It addresses the challenge of accurately segmenting indiv...
a cutting-edge cell segmentation model specifically designed for single-molecule resolved spatial omics datasets. It addresses the challenge of accurately segmenting individual cells in complex ima...
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Moritz Gerstung @moritzgerstung.bsky.social · 17/03/2025
Andrew Moorman and other members of @danapeer.bsky.social's lab helped carry out a rigorous assessment based on various 10x Xenium data sets with bespoke segmentation stainings, providing the ground truth to demonstrate segger's superior performance.
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Moritz Gerstung @moritzgerstung.bsky.social · 17/03/2025
Segger is a super fast graph neural network algorithm, which makes cell segmentation much more reliable and faster.
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Moritz Gerstung @moritzgerstung.bsky.social · 17/03/2025
Spatial transcriptomics holds great promise to understand biological tissue function, but the assignment of transcripts to cells has been a substantial bottleneck. For this reason, Elyas Heidari, a student in my lab and in @steglelab.bsky.social built segger. www.biorxiv.org/content/10.1...
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Daniel MacArthur @dgmacarthur.bsky.social · 15/03/2025
New preprint! We worked with @msftresearch.bsky.social and @broadinstitute.org to see whether large language models (LLMs) can be useful to variant scientists in deciding whether genetic variants seen in a patient are responsible for their disease. tl;dr yes they can: www.biorxiv.org/content/10.1...
biorxiv.org
Evidence Aggregator: AI reasoning applied to rare disease diagnostics
Retrieving, reviewing, and synthesizing technical information can be time-consuming and challenging, particularly when requiring specialized expertise, as is the case of variant assessment for rare di...
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Reposted by Moritz Gerstung
George Davey Smith @mendelrandom.bsky.social · 23/01/2025
Looking forward to @moritzgerstung.bsky.social seminar @uob-ieu.bsky.social on 30th Jan 2025 at 1pm, ,“ Using AI to Predict Disease Risks” in person and on line bristol-ac-uk.zoom.us/j/94273829130
bristol-ac-uk.zoom.us
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Moritz Gerstung @moritzgerstung.bsky.social · 20/11/2024
Amazing work. We‘re all walking laboratories for somatic evolution.
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Reposted by Moritz Gerstung
Inigo Martincorena @imartincorena.bsky.social · 20/11/2024
Resharing here a recent X post. In this preprint, we introduce an improved version of NanoSeq, a duplex sequencing protocol with <5 errors per billion bp in single DNA molecules, and use it to study the somatic mutation landscape of oral epithelium in >1000 people. 1/ www.medrxiv.org/content/10.1...
medrxiv.org
Somatic mutation and selection at epidemiological scale
As we age, many tissues become colonised by microscopic clones carrying somatic driver mutations ([1][1]–[10][2]. Some of these clones represent a first step towards cancer whereas others may contribu...
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Moritz Gerstung @moritzgerstung.bsky.social · 20/11/2024
Safe travels! We’re still waiting for the snow you got yesterday to arrive but chances look slim. Probably better travel wise.
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Moritz Gerstung @moritzgerstung.bsky.social · 18/11/2024
Thanks. Was on a bit of a social media hiatus, but this place looks like a new hope.
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Moritz Gerstung @moritzgerstung.bsky.social · 18/11/2024
Congratulations! Looking forward to seeing the outputs of your scientific ingenuity becoming multiplied.
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Reposted by Moritz Gerstung
Altmetric @altmetric.com · 18/11/2024
We strongly suggest that academic publishers and other platforms that host research rapidly implement a Share to Bluesky button for their articles. Here's how: docs.bsky.app/docs/advance... #AcademicSky #HigherEd #Altmetrics
docs.bsky.app
Action Intent Links | Bluesky
Authors, websites, and apps can use action intent links to implement "Share on Bluesky" buttons, or similar in-app actions. Logged-in users will be directed to the corresponding action view in the Blu...
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Moritz Gerstung @moritzgerstung.bsky.social · 18/11/2024
3/3 Paion is a new algorithm to diagnose brain cancers from H&E images. * distinguishes 102 types of brain cancer * high confidence predictions in 50-70% of cases across 7 cohorts * top1 acc > 85% in high conf subset * 2 day turnaround v 3 weeks for molecular testing Preprint coming soon.
Example Paion report for a confirmed myxopapillary ependymoma diagnosis. Shown are H&E, prediction heatmaps and automatically selected representative image tiles.
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Moritz Gerstung @moritzgerstung.bsky.social · 18/11/2024
2/3 Delphi-2M generative AI model for multi-disease risks * a single GPT-derived model learns risks of 1257 diseases * samples future life courses * offers insights into multi-morbidity dynamics www.medrxiv.org/content/10.1...
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Moritz Gerstung @moritzgerstung.bsky.social · 18/11/2024
1/3 Cancer risk models based on national health registries * trained 6.7M individuals from DK * validate in UK * disease history most important predictor for age >65 * family history predicts early onset cancers www.thelancet.com/journals/lan...
thelancet.com
Multi-cancer risk stratification based on national health data: a retrospective modelling and validation study
Data available in national electronic health databases can be used to approximate cancer risk factors and enable risk predictions in most cancer types. Model predictions generalise between the Danish ...
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Moritz Gerstung @moritzgerstung.bsky.social · 18/11/2024
5:20 start this morning for a virtual talk at the WEHI in Melbourne, covering: * Cancer risk models * Delphi multi-disease genAI * Paion, a new brain tumor digital pathology algorithm Summary below:
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Eric Topol @erictopol.bsky.social · 14/11/2024
New at Science Evo, a large language of life (LLLM) genomic foundation model, predicting & generating tasks from molecular to genomic scale science.org/doi/10.1126/...
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Moritz Gerstung @moritzgerstung.bsky.social · 15/11/2024
Long-term collaborator @ewanbirney.bsky.social is recruiting a joint postdoc with us to work on extensions of our Delphi generative health model. The post is based in Cambridge, UK. www.embl.org/jobs/positio...
embl.org
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