Evidence map›Paper›PMID 33008305›Full record

ArticleBMC bioinformatics2020

C3: connect separate connected components to form a succinct disease module.

Bingbo Wang, Jie Hu, Yajun Wang, Chenxing Zhang, Yuanjun Zhou, Liang Yu, Xingli Guo, Lin Gao, Yunru Chen

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Non-Coding RNAs Extended Omnigenic Module of Cancers.Entropy (Basel, Switzerland) · 2024
    Article
  2. Multi-omics peripheral and core regions of cancer.NPJ systems biology and applications · 2022
    Article
  3. Article
  4. Conserved Control Path in Multilayer Networks.Entropy (Basel, Switzerland) · 2022
    Article
4 · The record

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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.

Bingbo WangSchool of Computer Science and Technology, Xidian University, Xi'an, People's Republic of China. bingbowang@xidian.edu.cn.ORCID http://orcid.org/0000-0002-1808-1852
Jie HuSchool of Computer Science and Technology, Xidian University, Xi'an, People's Republic of China.
Yajun WangSchool of Humanities and Foreign Languages, Xi'an University of Technology, Xi'an, People's Republic of China.
Chenxing ZhangSchool of Computer Science and Technology, Xidian University, Xi'an, People's Republic of China.
Yuanjun ZhouSchool of Computer Science and Technology, Xidian University, Xi'an, People's Republic of China.
Liang YuSchool of Computer Science and Technology, Xidian University, Xi'an, People's Republic of China.
Xingli GuoSchool of Computer Science and Technology, Xidian University, Xi'an, People's Republic of China.
Lin GaoSchool of Computer Science and Technology, Xidian University, Xi'an, People's Republic of China.
Yunru ChenThe First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, People's Republic of China. chenyunru_2002@xjtu.edu.cn.

Funding

National Natural Science Foundation of China 61532014National Natural Science Foundation of China 61672406National Natural Science Foundation of China 61672407National Natural Science Foundation of China 61702396National Natural Science Foundation of China 61702397National Natural Science Foundation of China 61772395Shanghai Municipal Science and Technology Major Project 2018SHZDZX01
6 · The paper itself

Abstract

backgroundPrecise disease module is conducive to understanding the molecular mechanism of disease causation and identifying drug targets. However, due to the fragmentization of disease module in incomplete human interactome, how to determine connectivity pattern and detect a complete neighbourhood of disease based on this is still an open question.

resultsIn this paper, we perform exploratory analysis leading to an important observation that through a few intermediate nodes, most separate connected components formed by disease-associated proteins can be effectively connected and eventually form a complete disease module. And based on the topological properties of these intermediate nodes, we propose a connect separate connected components (C3) method to detect a succinct disease module by introducing a relatively small number of intermediate nodes, which allows us to obtain more pure disease module than other methods. Then we apply C3 across a large corpus of diseases to validate this connectivity pattern of disease module. Furthermore, the connectivity of the perturbed genes in multi-omics data such as The Cancer Genome Atlas also fits this pattern.

conclusionsC3 tool is not only useful in detecting a clearly-defined connected disease neighbourhood of 299 diseases and cancer with multi-omics data, but also helpful in better understanding the interconnection of phenotypically related genes in different omics data and studying complex pathological processes.

Indexed as

AlgorithmsDiseaseAsthmaBreast NeoplasmsFemaleGene OntologyHumansMolecular Sequence AnnotationProtein Interaction MapsProteinsProteinsBiological networkConnectivity patternDisease module

Identifiers

PMID33008305
PMCPMC7531168

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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.