Evidence map›Paper›PMID 40835864›Full record

ArticleScientific reports2025

Using transcripts to refine image based cell segmentation with FastReseg.

Lidan Wu, Joseph M Beechem, Patrick Danaher

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  3. Review
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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

3 authors.

Lidan WuBruker Spatial Biology, Seattle, WA, 98105, USA.
Joseph M BeechemBruker Spatial Biology, Seattle, WA, 98105, USA.
Patrick DanaherBruker Spatial Biology, Seattle, WA, 98105, USA. patrick.danaher@bruker.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spatial transcriptomics (ST) faces persistent challenges in cell segmentation accuracy, which can bias biological interpretations in a spatial-dependent way. FastReseg introduces a novel algorithm that refines inaccuracies in existing image-based segmentations using transcriptomic data, without radically redefining cell boundaries. By combining image-based information with 3D transcriptomic precision, FastReseg enhances segmentation accuracy. Its key innovation, a transcript scoring system based on log-likelihood ratios, facilitates the quick identification and correction of spatial doublets caused by cell proximity or overlap in 2D. FastReseg reduces circularity in boundary derivation, and addresses computational challenges with a modular workflow designed for large datasets. The algorithm's modularity allows for seamless optimization and integration of advancements in segmentation technology. FastReseg provides a scalable, efficient solution to improve the quality and interpretability of ST data, ensuring compatibility with evolving segmentation methods and enabling more accurate biological insights.

Indexed as

Cell SeparationGene Expression ProfilingImage Processing, Computer-AssistedAlgorithmsHumansSupport Vector Machine

Identifiers

PMID40835864
PMCPMC12368049

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.