Evidence map›Paper›PMID 32373160›Full record

ArticleFrontiers in genetics2020

Predicting the Disease Genes of Multiple Sclerosis Based on Network Representation Learning.

Haijie Liu, Jiaojiao Guan, He Li, Zhijie Bao, Qingmei Wang, Xun Luo, Hansheng Xue

Abstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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.

Haijie LiuDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Jiaojiao GuanSchool of Computer Science, Northwestern Polytechnical University, Xi'an, China.
He LiDepartment of Automation, College of Information Science and Engineering, Tianjin Tianshi College, Tianjin, China.
Zhijie BaoSchool of Textile Science and Engineering, Tiangong University, Tianjin, China.
Qingmei WangStroke Biological Recovery Laboratory, Department of Physical Medicine and Rehabilitation, Spaulding Rehabilitation Hospital, The Teaching Affiliate of Harvard Medical School Charlestown, Boston, MA, United States.
Xun LuoKerry Rehabilitation Medicine Research Institute, Shenzhen, China.
Hansheng XueSchool of Computer Science, Northwestern Polytechnical University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an autoimmune disease for which it is difficult to find exact disease-related genes. Effectively identifying disease-related genes would contribute to improving the treatment and diagnosis of multiple sclerosis. Current methods for identifying disease-related genes mainly focus on the hypothesis of guilt-by-association and pay little attention to the global topological information of the whole protein-protein-interaction (PPI) network. Besides, network representation learning (NRL) has attracted a huge amount of attention in the area of network analysis because of its promising performance in node representation and many downstream tasks. In this paper, we try to introduce NRL into the task of disease-related gene prediction and propose a novel framework for identifying the disease-related genes multiple sclerosis. The proposed framework contains three main steps: capturing the topological structure of the PPI network using NRL-based methods, encoding learned features into low-dimensional space using a stacked autoencoder, and training a support vector machine (SVM) classifier to predict disease-related genes. Compared with three state-of-the-art algorithms, our proposed framework shows superior performance on the task of predicting disease-related genes of multiple sclerosis.

Indexed as

deep learningdisease gene predictionmultiple sclerosisnetwork embeddingPPI network

Identifiers

PMID32373160
PMCPMC7186413

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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.