Evidence map›Paper›PMID 41831446›Full record

ArticleCell reports methods2026

Practical AI-based cell extraction and spatial statistics for large 3D bone marrow tissue images.

George Adams, Floriane S Tissot, Chang Liu, Cera Mai, Chris Brunsdon, Ken R Duffy, Cristina Lo Celso

Abstract read
In one paragraph

Article in Cell reports methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

George AdamsDepartment of Life Sciences, Sir Alexander Fleming Building, Imperial College London, London SW7 2AZ, UK; Centre for Haematology, Department of Immunology and Inflammation, Imperial College London, London W12 0NN, UK.
Floriane S TissotDepartment of Life Sciences, Sir Alexander Fleming Building, Imperial College London, London SW7 2AZ, UK; Centre for Haematology, Department of Immunology and Inflammation, Imperial College London, London W12 0NN, UK; The Francis Crick Institute, London WC2A 3LY, UK.
Chang LiuHamilton Institute, Maynooth University, Maynooth, Co. Kildare, Ireland.
Cera MaiDepartment of Life Sciences, Sir Alexander Fleming Building, Imperial College London, London SW7 2AZ, UK; Centre for Haematology, Department of Immunology and Inflammation, Imperial College London, London W12 0NN, UK; The Francis Crick Institute, London WC2A 3LY, UK.
Chris BrunsdonNational Centre for Geocomputation, Maynooth University, Maynooth, Co. Kildare, Ireland.
Ken R DuffyDepartment of Electrical and Computer Engineering, Northeastern University, Boston, MA 02115, USA; Department of Mathematics, Northeastern University, Boston, MA 02115, USA. Electronic address: k.duffy@northeastern.edu.
Cristina Lo CelsoDepartment of Life Sciences, Sir Alexander Fleming Building, Imperial College London, London SW7 2AZ, UK; Centre for Haematology, Department of Immunology and Inflammation, Imperial College London, London W12 0NN, UK; The Francis Crick Institute, London WC2A 3LY, UK. Electronic address: c.lo-celso@imperial.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the molecular regulation of hematopoiesis is well characterized, the spatial organization of hematopoietic cells within bone marrow (BM) remains unclear. Advances in microscopy have produced increasingly detailed images of murine BM, yet accurate and scalable methods to extract and analyze these complex datasets are limited. We present PACESS, a computational workflow for BM analysis that combines convolutional neural networks for 2D cell detection and classification with an automated method to extrapolate into 3D, spatial statistical analyses to define tissue regions based on local cell-type densities, and logistic regression to assess whether the relative abundances of cell types reflect reciprocal dependencies. Using PACESS, we investigate the spatial organization of T cells, megakaryocytes, and leukemic cells, revealing that distinct leukemic clusters generate diverse, previously unrecognized neighborhoods within the same BM cavity. PACESS, thus, provides a powerful tool to dissect BM architecture.

Indexed as

Artificial IntelligenceBone MarrowBone Marrow CellsImaging, Three-DimensionalAnimalsConvolutional Neural NetworksHumansMegakaryocytesMice3Dbone marrow tissue architecturecell clustersconvolutional neural networkCP: computational biologyCP: systems biologyleukemialymphocytesmegakaryocytesspatial statisticsthick histological preparationstissue clearing

Identifiers

PMID41831446
PMCPMC13030987

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.