Evidence map›Paper›PMID 35610556›Full record

ArticleBMC bioinformatics2022

Gene co-expression network based on part mutual information for gene-to-gene relationship and gene-cancer correlation analysis.

Yi-Hua Jiang, Jie Long, Zhi-Bin Zhao, Liang Li, Zhe-Xiong Lian, Zhi Liang, Jia-Rui Wu

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 31% of its field
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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Yi-Hua JiangHefei National Laboratory for Physical Sciences at Microscale and School of Life Science, University of Science and Technology of China, Hefei, China.
Jie LongChronic Disease Laboratory, School of Medicine, South China University of Technology, Guangzhou, China.
Zhi-Bin ZhaoChronic Disease Laboratory, School of Medicine, South China University of Technology, Guangzhou, China.
Liang LiChronic Disease Laboratory, School of Medicine, South China University of Technology, Guangzhou, China.
Zhe-Xiong LianChronic Disease Laboratory, School of Medicine, South China University of Technology, Guangzhou, China.
Zhi LiangHefei National Laboratory for Physical Sciences at Microscale and School of Life Science, University of Science and Technology of China, Hefei, China. liangzhi@ustc.edu.cn.
Jia-Rui WuHefei National Laboratory for Physical Sciences at Microscale and School of Life Science, University of Science and Technology of China, Hefei, China. wujr@sibs.ac.cn.
South China University of Technology · CNHefei National Center for Physical Sciences at Nanoscale · CNUniversity of Chinese Academy of Sciences · CNUniversity of Science and Technology of China · CN

Funding

Strategic Priority CAS Project XDB38000000
6 · The paper itself

Abstract

backgroundFinding correlation patterns is an important goal of analyzing biological data. Currently available methods for correlation analysis mainly use non-direct associations, such as the Pearson correlation coefficient, and focus on the interpretation of networks at the level of modules. For biological objects such as genes, their collective function depends on pairwise gene-to-gene interactions. However, a large amount of redundant results from module level methods often necessitate further detailed analysis of gene interactions. New approaches of measuring direct associations among variables, such as the part mutual information (PMI), may help us better interpret the correlation pattern of biological data at the level of variable pairs.

resultsWe use PMI to calculate gene co-expression networks of cancer mRNA transcriptome data. Our results show that the PMI-based networks with fewer edges could represent the correlation pattern and are robust across biological conditions. The PMI-based networks recall significantly more important parts of omics defined gene-pair relationships than the Pearson Correlation Coefficient (PCC)-based networks. Based on the scores derived from PMI-recalled copy number variation or DNA methylation gene-pairs, the patients with cancer can be divided into groups with significant differences on disease specific survival.

conclusionsPMI, measuring direct associations between variables, extracts more important biological relationships at the level of gene pairs than conventional indirect association measures do. It can be used to refine module level results from other correlation methods. Particularly, PMI is beneficial to analysis of biological data of the complicated systems, for example, cancer transcriptome data.

Indexed as

DNA Copy Number VariationsNeoplasmsCorrelation of DataGene Expression ProfilingGene Regulatory NetworksHumansTranscriptomeCancer survival analysisCorrelation analysisDirect associationMultiple omics integrationPart mutual information

Identifiers

PMID35610556
PMCPMC9128248
OpenAlexW4281929191

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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.