Evidence map›Paper›PMID 40567731›Full record

ArticlePeerJ. Computer science2025

Deep learning model for gastrointestinal polyp segmentation.

Zitong Wang, Zeyi Wang, Pengyu Sun

Abstract read
In one paragraph

Article in PeerJ. Computer science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. CAFrontiers in artificial intelligence · 2026
    Article
  3. Article
  4. 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

3 authors.

Zitong WangImperial College London, London, South Kensington, United Kingdom.
Zeyi WangQueen Mary University of London, London, Bethnal Green, United Kingdom.
Pengyu SunXidian University, Xi'an, Shannxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the biggest hazards to cancer-related mortality globally is colorectal cancer, and improved patient outcomes are greatly influenced by early identification. Colonoscopy is a highly effective screening method, yet segmentation and detection remain challenging aspects due to the heterogeneity and variability of readers' interpretations of polyps. In this work, we introduce a novel deep learning architecture for gastrointestinal polyp segmentation in the Kvasir-SEG dataset. Our method employs an encoder-decoder structure with a pre-trained ConvNeXt model as the encoder to learn multi-scale feature representations. The feature maps are passed through a ConvNeXt Block and then through a decoder network consisting of three decoder blocks. Our key contribution is the employment of a cross-attention mechanism that creates shortcut connections between the decoder and encoder to maximize feature retention and reduce information loss. In addition, we introduce a Residual Transformer Block in the decoder that learns long-term dependency by using self-attention mechanisms and enhance feature representations. We evaluate our model on the Kvasir-SEG dataset, achieving a Dice coefficient of 0.8715 and mean intersection over union (mIoU) of 0.8021. Our methodology demonstrates state-of-the-art performance in gastrointestinal polyp segmentation and its feasibility of being used as part of clinical pipelines to assist with automated detection and diagnosis of polyps.

Indexed as

Deep learningGastrointestinal polypImage segmentationKvasir-SEGTransformer

Identifiers

PMID40567731
PMCPMC12192692

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.