Evidence map›Paper›PMID 35884502›Full record

ArticleCancers2022

An Open-Source AI Framework for the Analysis of Single Cells in Whole-Slide Images with a Note on CD276 in Glioblastoma.

Islam Alzoubi, Guoqing Bao, Rong Zhang, Christina Loh, Yuqi Zheng, Svetlana Cherepanoff, Gary Gracie, Maggie Lee, Michael Kuligowski, Kimberley L Alexander and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.2field-weighted citation impact, top 9% of its field
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

6 citing papers in PubMed, 12 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Islam AlzoubiSchool of Computer Science, The University of Sydney, J12/1 Cleveland St, Sydney, NSW 2008, Australia.
Guoqing BaoSchool of Computer Science, The University of Sydney, J12/1 Cleveland St, Sydney, NSW 2008, Australia.ORCID 0000-0002-0669-6358
Rong ZhangSchool of Computer Science, The University of Sydney, J12/1 Cleveland St, Sydney, NSW 2008, Australia.
Christina LohKen Parker Brain Tumour Research Laboratories, Brain and Mind Centre, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW 2050, Australia.
Yuqi ZhengKen Parker Brain Tumour Research Laboratories, Brain and Mind Centre, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW 2050, Australia.
Svetlana CherepanoffSt Vincent's Hospital, Victoria Street, Darlinghurst, NSW 2010, Australia.
Gary GracieSt Vincent's Hospital, Victoria Street, Darlinghurst, NSW 2010, Australia.
Maggie LeeDepartment of Neuropathology, RPA Hospital and Brain and Mind Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.
Michael KuligowskiSydney Microscopy and Microanalysis, The University of Sydney, Sydney, NSW 2006, Australia.
Kimberley L AlexanderDepartment of Neuropathology, RPA Hospital and Brain and Mind Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.
Michael E BucklandDepartment of Neuropathology, RPA Hospital and Brain and Mind Centre, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.
Xiuying WangSchool of Computer Science, The University of Sydney, J12/1 Cleveland St, Sydney, NSW 2008, Australia.
Manuel B GraeberKen Parker Brain Tumour Research Laboratories, Brain and Mind Centre, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW 2050, Australia.
The University of Sydney · AUSt Vincent's Hospital Sydney · AU

Funding

Australian Research Council DP150104472
6 · The paper itself

Abstract

Routine examination of entire histological slides at cellular resolution poses a significant if not insurmountable challenge to human observers. However, high-resolution data such as the cellular distribution of proteins in tissues, e.g., those obtained following immunochemical staining, are highly desirable. Our present study extends the applicability of the PathoFusion framework to the cellular level. We illustrate our approach using the detection of CD276 immunoreactive cells in glioblastoma as an example. Following automatic identification by means of PathoFusion's bifocal convolutional neural network (BCNN) model, individual cells are automatically profiled and counted. Only discriminable cells selected through data filtering and thresholding were segmented for cell-level analysis. Subsequently, we converted the detection signals into the corresponding heatmaps visualizing the distribution of the detected cells in entire whole-slide images of adjacent H&E-stained sections using the Discrete Wavelet Transform (DWT). Our results demonstrate that PathoFusion is capable of autonomously detecting and counting individual immunochemically labelled cells with a high prediction performance of 0.992 AUC and 97.7% accuracy. The data can be used for whole-slide cross-modality analyses, e.g., relationships between immunochemical signals and anaplastic histological features. PathoFusion has the potential to be applied to additional problems that seek to correlate heterogeneous data streams and to serve as a clinically applicable, weakly supervised system for histological image analyses in (neuro)pathology.

Indexed as

artificial intelligencebifocal convolutional neural network (BCNN)CD276image fusionimage segmentationPathoFusion framework

Identifiers

PMID35884502
PMCPMC9316952
OpenAlexW4285733581

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.