Evidence map›Paper›PMID 42007518›Full record

ArticleBriefings in bioinformatics2026

GALA: a unified landmark-free framework for coarse-to-fine spatial alignment across resolutions and modalities in spatial transcriptomics.

Tao Ding, Pengcheng Zeng

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 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

2 authors.

Tao DingInstitute of Mathematical Sciences, ShanghaiTech University, 393 Middle Huaxia Road, Pudong New Area, Shanghai, 201210, China.
Pengcheng ZengInstitute of Mathematical Sciences, ShanghaiTech University, 393 Middle Huaxia Road, Pudong New Area, Shanghai, 201210, China.

Funding

High-Performance Computing (HPC) platform at ShanghaiTech University
6 · The paper itself

Abstract

Spatial transcriptomics alignment is challenged by technical variations, including geometric distortions from tissue preparation and platform-driven differences in resolution and modality. These issues create diverse alignment scenarios, from matched and mismatched resolutions to cross-modality integration, while partial tissue coverage further complicates the task. To overcome these limitations, we introduce GALA (Genetic Algorithm-guided Large Deformation Alignment), a unified, landmark-free framework that couples global affine transformation and local diffeomorphic deformation within a single optimization. Its modality-aware rasterization harmonizes transcriptomic and histological data into a shared grid, enabling landmark-free, multimodal alignment across resolutions, and modalities. Evaluated on diverse human and mouse datasets, GALA outperforms existing methods in accuracy, computational efficiency, and biological interpretability for both complete and partial tissue alignment.

Indexed as

AlgorithmsGene Expression ProfilingImage Processing, Computer-AssistedTranscriptomeAnimalsGenetic AlgorithmsHumansMiceSpatial Transcriptomicsdiffeomorphic deformationgenetic algorithmimage registrationmultimodal integrationspatial transcriptomics alignment

Identifiers

PMID42007518
PMCPMC13093224

What OpenQuestion holds

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LicenceCC BY
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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.