Evidence map›Paper›PMID 31865913›Full record

ArticleBMC medical genomics2019

Heterogeneous network embedding enabling accurate disease association predictions.

Yun Xiong, Mengjie Guo, Lu Ruan, Xiangnan Kong, Chunlei Tang, Yangyong Zhu, Wei Wang

Abstract read
In one paragraph

Article in BMC medical genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  4. Review
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  7. Biology and medicine in the landscape of quantum advantages.Journal of the Royal Society, Interface · 2022
    Review
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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.

Yun XiongShanghai Key Laboratory of Data Science, School of Computer Science, Fudan University, Shanghai, China.
Mengjie GuoShanghai Key Laboratory of Data Science, School of Computer Science, Fudan University, Shanghai, China.
Lu RuanShanghai Key Laboratory of Data Science, School of Computer Science, Fudan University, Shanghai, China.
Xiangnan KongDepartment of Computer Science, Worcester Polytechnic Institute, Worcester, USA.
Chunlei TangBrigham and Women's Hospital, Harvard Medical School, Boston, USA.
Yangyong ZhuShanghai Key Laboratory of Data Science, School of Computer Science, Fudan University, Shanghai, China.
Wei WangDepartment of Computer Science, Scalable Analytics Institute (ScAi), University of California, Los Angeles, USA. weiwang@cs.ucla.edu.

Funding

TRAININGU54GM114833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LINDSEY, MERRY L., PING, PEIPEI · 2014 to 2017
$13.8M
Fast and Robust Methods for Large Scale Genotype Phenotype Association StudyR01GM115833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, WEI · 2015 to 2017
$933k
NIGMS NIH HHS R01 GM115833NIGMS NIH HHS U54 GM114833
6 · The paper itself

Abstract

backgroundIt is significant to identificate complex biological mechanisms of various diseases in biomedical research. Recently, the growing generation of tremendous amount of data in genomics, epigenomics, metagenomics, proteomics, metabolomics, nutriomics, etc., has resulted in the rise of systematic biological means of exploring complex diseases. However, the disparity between the production of the multiple data and our capability of analyzing data has been broaden gradually. Furthermore, we observe that networks can represent many of the above-mentioned data, and founded on the vector representations learned by network embedding methods, entities which are in close proximity but at present do not actually possess direct links are very likely to be related, therefore they are promising candidate subjects for biological investigation.

resultsWe incorporate six public biological databases to construct a heterogeneous biological network containing three categories of entities (i.e., genes, diseases, miRNAs) and multiple types of edges (i.e., the known relationships). To tackle the inherent heterogeneity, we develop a heterogeneous network embedding model for mapping the network into a low dimensional vector space in which the relationships between entities are preserved well. And in order to assess the effectiveness of our method, we conduct gene-disease as well as miRNA-disease associations predictions, results of which show the superiority of our novel method over several state-of-the-arts. Furthermore, many associations predicted by our method are verified in the latest real-world dataset.

conclusionsWe propose a novel heterogeneous network embedding method which can adequately take advantage of the abundant contextual information and structures of heterogeneous network. Moreover, we illustrate the performance of the proposed method on directing studies in biology, which can assist in identifying new hypotheses in biological investigation.

Indexed as

DiseaseComputational BiologyHumansDisease association predictionHeterogeneous networkNetwork embedding

Identifiers

PMID31865913
PMCPMC6927100

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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.