Evidence map›Paper›PMID 41676373›Full record

ArticleQuantitative biology (Beijing, China)2024

A feature extraction framework for discovering pan-cancer driver genes based on multi-omics data.

Xiaomeng Xue, Feng Li, Junliang Shang, Lingyun Dai, Daohui Ge, Qianqian Ren

Abstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 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

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

1 citing paper in PubMed.

  1. 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

6 authors.

Xiaomeng XueSchool of Computer Science Qufu Normal University Rizhao China.ORCID https://orcid.org/0009-0007-1233-0938
Feng LiSchool of Computer Science Qufu Normal University Rizhao China.
Junliang ShangSchool of Computer Science Qufu Normal University Rizhao China.
Lingyun DaiSchool of Computer Science Qufu Normal University Rizhao China.
Daohui GeSchool of Computer Science Qufu Normal University Rizhao China.
Qianqian RenSchool of Computer Science Qufu Normal University Rizhao China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of tumor driver genes facilitates accurate cancer diagnosis and treatment, playing a key role in precision oncology, along with gene signaling, regulation, and their interaction with protein complexes. To tackle the challenge of distinguishing driver genes from a large number of genomic data, we construct a feature extraction framework for discovering pan-cancer driver genes based on multi-omics data (mutations, gene expression, copy number variants, and DNA methylation) combined with protein-protein interaction (PPI) networks. Using a network propagation algorithm, we mine functional information among nodes in the PPI network, focusing on genes with weak node information to represent specific cancer information. From these functional features, we extract distribution features of pan-cancer data, pan-cancer TOPSIS features of functional features using the ideal solution method, and SetExpan features of pan-cancer data from the gene functional features, a method to rank pan-cancer data based on the average inverse rank. These features represent the common message of pan-cancer. Finally, we use the lightGBM classification algorithm for gene prediction. Experimental results show that our method outperforms existing methods in terms of the area under the check precision-recall curve (AUPRC) and demonstrates better performance across different PPI networks. This indicates our framework's effectiveness in predicting potential cancer genes, offering valuable insights for the diagnosis and treatment of tumors.

Indexed as

cancer driver genesfeature extractionmulti‐omics datanetwork propagationpan‐cancer

Identifiers

PMID41676373
PMCPMC12806351

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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.