Evidence map›Paper›PMID 38761803›Full record

ArticleCell reports methods2024

Subtype-WGME enables whole-genome-wide multi-omics cancer subtyping.

Hai Yang, Liang Zhao, Dongdong Li, Congcong An, Xiaoyang Fang, Yiwen Chen, Jingping Liu, Ting Xiao, Zhe Wang

Abstract read
In one paragraph

Article in Cell reports methods, 2024. 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. Article
  3. Review
  4. Review
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

9 authors.

Hai YangDepartment of Computer Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Liang ZhaoDepartment of Computer Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Dongdong LiDepartment of Computer Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Congcong AnDepartment of Computer Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Xiaoyang FangCornell Tech, Cornell University, New York, NY 14853, USA.
Yiwen ChenCenter for Continuing and Lifelong Education, National University of Singapore, Singapore 119077, Singapore.
Jingping LiuDepartment of Computer Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Ting XiaoDepartment of Computer Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Zhe WangDepartment of Computer Science and Engineering, East China University of Science and Technology, Shanghai 200237, China. Electronic address: wangzhe@ecust.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present an innovative strategy for integrating whole-genome-wide multi-omics data, which facilitates adaptive amalgamation by leveraging hidden layer features derived from high-dimensional omics data through a multi-task encoder. Empirical evaluations on eight benchmark cancer datasets substantiated that our proposed framework outstripped the comparative algorithms in cancer subtyping, delivering superior subtyping outcomes. Building upon these subtyping results, we establish a robust pipeline for identifying whole-genome-wide biomarkers, unearthing 195 significant biomarkers. Furthermore, we conduct an exhaustive analysis to assess the importance of each omic and non-coding region features at the whole-genome-wide level during cancer subtyping. Our investigation shows that both omics and non-coding region features substantially impact cancer development and survival prognosis. This study emphasizes the potential and practical implications of integrating genome-wide data in cancer research, demonstrating the potency of comprehensive genomic characterization. Additionally, our findings offer insightful perspectives for multi-omics analysis employing deep learning methodologies.

Indexed as

Biomarkers, TumorGenomicsNeoplasmsAlgorithmsComputational BiologyGenome, HumanGenome-Wide Association StudyHumansMultiomicsPrognosisBiomarkers, Tumorcancer biomarkersCP: Cancer biologyCP: Systems biologydeep learning methodsmolecular subtypingmulti-omics data integrationwhole-genome

Identifiers

PMID38761803
PMCPMC11228280

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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.