Evidence map›Paper›PMID 40501614›Full record

ArticlebioRxiv : the preprint server for biology2025

Graphical and Interactive Spatial Proteomics Image Analysis Workflow.

Pritpal Singh, Jocelyn H Wright, Kimberly S Smythe, Bryce Fukuda, Ling-Hong Hung, Cecilia Cs Yeung, Ka Yee Yeung

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

7 authors.

Pritpal SinghSchool of Engineering and Technology, University of Washington Tacoma, WA.
Jocelyn H WrightSchool of Engineering and Technology, University of Washington Tacoma, WA.ORCID 0000-0003-1548-0847
Kimberly S SmytheSchool of Engineering and Technology, University of Washington Tacoma, WA.ORCID 0000-0002-2329-8298
Bryce FukudaSchool of Engineering and Technology, University of Washington Tacoma, WA.ORCID 0009-0003-7203-5261
Ling-Hong HungSchool of Engineering and Technology, University of Washington Tacoma, WA.ORCID 0000-0002-5209-2248
Cecilia Cs YeungSchool of Engineering and Technology, University of Washington Tacoma, WA.ORCID 0000-0001-6799-2022
Ka Yee YeungSchool of Engineering and Technology, University of Washington Tacoma, WA.ORCID 0000-0002-1754-7577

Funding

MorPhiC Data Resource and Administrative Coordinating CenterU24HG012674 · NHGRI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Helen Elizabeth Parkinson, Stephan C Schurer · 2022 to 2026
$6.9M
Biomarkers for optimizing risk prediction and early detection of cancers of the colon and esophagusU2CCA271902 · NCI · FRED HUTCHINSON CANCER CENTER · PI Cecilia C Yeung · 2022 to 2026
$5.3M
Rapid Acute Leukemia Genomic Profiling with CRISPR enrichment and Real-time long-read sequencingR21CA280520 · NCI · FRED HUTCHINSON CANCER CENTER · PI YEUNG, CECILIA C · 2023 to 2024
$687k
NCI NIH HHS R21 CA280520NCI NIH HHS U2C CA271902NHGRI NIH HHS U24 HG012674
6 · The paper itself

Abstract

Spatial proteomics provides a spatially resolved view of protein expression and localization within cells and tissues by mapping the location and abundance of proteins. There is a need for fully-integrated end-to-end imaging workflows for spatial proteomic analysis that are flexible, high-throughput, and support graphical and interactive visualizations. We present a modular and interactive spatial proteomic image analysis workflow with individual steps containerized that empowers biomedical researchers to reproducibly execute and customize complex analyses. Our workflow consists of cell segmentation, unsupervised clustering, validation of clusters on the image, and cell type clustering results visualization. Users can utilize a form-based graphical interface to execute and customize multi-step workflows with a single click or interactively adjust image processing steps within the workflow, apply workflows to various datasets, and modify input parameters as needed. We illustrated the functionality of our workflow using a cancer imaging dataset consisting of a tissue microarray (TMA) stained by high-plex immunohistochemistry. This TMA contained a variety of cancer and tissue cell types to assess the broad applicability of this workflow to different biopsy and tissue types.

Identifiers

PMID40501614
PMCPMC12154974

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.