Evidence map›Paper›PMID 41629719›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Artificial Intelligence-Driven Laser Capture Microdissection.

Tommaso Gasparello, Matthew Pearson, Alex von Kriegsheim

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 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

3 authors.

Tommaso GasparelloInstitute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Matthew PearsonInstitute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Alex von KriegsheimInstitute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK. Alex.VonKriegsheim@ed.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laser capture microdissection enables precise isolation of regions of interest (ROIs) from tissue sections, allowing researchers to investigate tissue heterogeneity with spatial resolution. This technique has been integrated with various omics approaches, including transcriptomics and proteomics, to enhance sensitivity and expand coverage beyond traditional bulk analysis methods. Among these, mass spectrometry (MS)-based proteomics has emerged as a particularly powerful tool by enabling the reliable identification of even low-abundance proteins and facilitating the discovery of novel disease biomarkers.Recently, both laser capture microdissection and MS-based proteomics have been significantly shaped by the rapid advancement and widespread adoption of artificial intelligence (AI). In fact, deep learning, a subfield of AI, has been used to improve bioimage analysis for ROI selection in laser capture microdissection workflows. Concurrently, AI-based methods are increasingly being used to manage and interpret high-dimensional data generated by MS-based proteomics, further enhancing analytical depth and reproducibility.Despite this progress, current workflows often lack scalability and flexibility, limiting their broader application in clinical and translational settings. To address these challenges, we have developed an AI-driven laser capture microdissection protocol optimized for hematoxylin and eosin (H&E)-stained slides derived from formalin-fixed paraffin-embedded (FFPE) patient samples. The widespread availability of FFPE tissues and the simplicity of H&E staining make this approach both accessible and adaptable for investigating diverse disease contexts, with the potential to advance spatial proteomics at scale.

Indexed as

Artificial IntelligenceLaser Capture MicrodissectionProteomicsHumansIntelligent SystemsMass SpectrometryParaffin EmbeddingStaining and LabelingTissue FixationWorkflowArtificial intelligenceDeep visual proteomicsFormalin-fixed paraffin-embeddedHematoxylin and eosinLaser capture microdissectionMass spectrometry-based proteomicsSpatial proteomics

Identifiers

What OpenQuestion holds

Textmetadata
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.