Evidence map›Paper›PMID 40662796›Full record

ArticleBioinformatics (Oxford, England)2025

Anomaly detection in spatial transcriptomics via spatially localized density comparison.

Gary Hu, Julian Gold, Uthsav Chitra, Sunay Joshi, Benjamin J Raphael

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Powerful and accurate case-control analysis of spatial molecular data.bioRxiv : the preprint server for biology · 2025
    Article
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

5 authors.

Gary HuDepartment of Computer Science, Princeton University, Princeton, NJ, 08540, United States.
Julian GoldCenter for Statistics and Machine Learning, Princeton University, Princeton, NJ, 08540, United States.
Uthsav ChitraEric and Wendy Schmidt Center, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, United States.ORCID 0000-0001-6016-0960
Sunay JoshiDepartment of Applied Mathematics and Computational Sciences, University of Pennsylvania, Philadelphia, PA, 19104, United States.
Benjamin J RaphaelDepartment of Computer Science, Princeton University, Princeton, NJ, 08540, United States.ORCID 0000-0003-1274-048X

Funding

Comprehensive and Robust Tools for Analysis of Tumor Heterogeneity and EvolutionU24CA248453 · NCI · PRINCETON UNIVERSITY · PI Benjamin Raphael · 2020 to 2026
$4.7M
Pathway, Network and Spatiotemporal Integration of Cancer Genomics DataU24CA264027 · NCI · PRINCETON UNIVERSITY · PI RAPHAEL, BENJAMIN, YEH, JEN JEN · 2021 to 2025
$1.5M
Broad Institute of MIT and HarvardEric and Wendy Schmidt CenterNCI NIH HHS U24 CA248453NCI NIH HHS U24CA248453NCI NIH HHS U24 CA264027NCI NIH HHS U24CA264027Schmidt DataX Fund at Princeton UniversitySchmidt Futures Foundation
6 · The paper itself

Abstract

motivationPerturbations in biological tissues-e.g. due to inflammation, disease, or drug treatment-alter the composition of cell types and cell states in the tissue. These alterations are often spatially localized in different regions of a tissue, and can be measured using spatial transcriptomics technologies. However, current methods to analyze differential abundance in cell types or cell states, either do not incorporate spatial information-and thus cannot identify spatially localized alterations-or use heuristic and inaccurate approaches.

resultsWe introduce Spatial Anomaly Region Detection in Expression Manifolds (Sardine), a method to estimate spatially localized changes in spatial transcriptomics data obtained from tissue slices from two or more conditions. Sardine estimates the probability of a cell state being at the same (relative) spatial location between different conditions using spatially localized density estimation. On simulated data, Sardine recapitulates the spatial patterning of expression changes more accurately than existing approaches. On a Visium dataset of the mouse cerebral cortex before and after injury response, as well as on a Visium dataset of a mouse spinal cord undergoing electrotherapy, Sardine identifies regions of spatially localized expression changes that are more biologically plausible than alternative approaches. AVAILABILITY AND IMPLEMENTATION: We implement Sardine in Python 3, with an open source implementation available at: https://github.com/raphael-group/spatial_anomaly_detection.

Indexed as

Computational BiologyGene Expression ProfilingTranscriptomeAlgorithmsAnimalsCerebral CortexMiceSpinal Cord

Identifiers

PMID40662796
PMCPMC12261494

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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.