Evidence map›Paper›PMID 39698468›Full record

ArticleFrontiers in genetics2024

Gene expression ranking change based single sample pre-disease state detection.

Zhenshen Bao, Xianbin Li, Peng Xu, Xiangzhen Zan

Abstract read
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Article in Frontiers in genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Zhenshen BaoSchool of Information Engineering, Taizhou University, Taizhou, Jiangsu, China.
Xianbin LiSchool of Computer and Big Data Science, Jiujiang University, Jiujiang, Jiangxi, China.
Peng XuInstitute of computational science and technology, Guangzhou University, Guangzhou, Guangdong, China.
Xiangzhen ZanSchool of Cultural and Creative Trade, Shenzhen Pengcheng Technician College, Shenzhen, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: To prevent disease, it is of great importance to detect the critical point (pre-disease state) when the biological system abruptly transforms from normal to disease state. However, rapid and accurate pre-disease state detection is still a challenge when there is only a single sample available. The state transition of the biological system is driven by the variation in regulations between genes. Methods: In this study, we propose a rapid single-sample pre-disease state-identifying method based on the change in gene expression ranking, which can reflect the coordinated shifts between genes, that is, S-PCR. The R codes of S-PCR can be accessed at https://github.com/ZhenshenBao/S-PCR. Results: This model-free method is validated by the successful identification of pre-disease state for both simulated and five real datasets. The functional analyses of the pre-disease state-related genes identified by S-PCR also demonstrate the effectiveness of this computational approach. Furthermore, the time efficiency of S-PCR is much better than that of its peers. Discussion: Hence, the proposed S-PCR approach holds immense potential for clinical applications in personalized disease diagnosis.

Indexed as

personalized disease diagnosispre-disease stateranking changesingle samplestate transition

Identifiers

PMID39698468
PMCPMC11652538

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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.