Evidence map›Paper›PMID 28255556›Full record

ArticleBioMed research international2017

Identifying and Analyzing Novel Epilepsy-Related Genes Using Random Walk with Restart Algorithm.

Wei Guo, Dong-Mei Shang, Jing-Hui Cao, Kaiyan Feng, Yi-Chun He, Yang Jiang, ShaoPeng Wang, Yu-Fei Gao

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

8 authors at 3 institutions in 1 country.

Wei GuoDepartment of Outpatient, China-Japan Union Hospital of Jilin University, Changchun 130033, China.
Dong-Mei ShangDepartment of Outpatient, China-Japan Union Hospital of Jilin University, Changchun 130033, China.
Jing-Hui CaoDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun 130033, China.
Kaiyan FengDepartment of Computer Science, Guangdong AIB Polytechnic, Guangzhou 510507, China.
Yi-Chun HeDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun 130033, China.ORCID 0000-0001-5883-9384
Yang JiangDepartment of Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, China.ORCID 0000-0002-1901-9778
ShaoPeng WangSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Yu-Fei GaoDepartment of Neurosurgery, China-Japan Union Hospital of Jilin University, Changchun 130033, China.ORCID 0000-0002-4411-9965
Union Hospital · CNGuangdong Polytechnic Normal University · CNShanghai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a pathological condition, epilepsy is caused by abnormal neuronal discharge in brain which will temporarily disrupt the cerebral functions. Epilepsy is a chronic disease which occurs in all ages and would seriously affect patients' personal lives. Thus, it is highly required to develop effective medicines or instruments to treat the disease. Identifying epilepsy-related genes is essential in order to understand and treat the disease because the corresponding proteins encoded by the epilepsy-related genes are candidates of the potential drug targets. In this study, a pioneering computational workflow was proposed to predict novel epilepsy-related genes using the random walk with restart (RWR) algorithm. As reported in the literature RWR algorithm often produces a number of false positive genes, and in this study a permutation test and functional association tests were implemented to filter the genes identified by RWR algorithm, which greatly reduce the number of suspected genes and result in only thirty-three novel epilepsy genes. Finally, these novel genes were analyzed based upon some recently published literatures. Our findings implicate that all novel genes were closely related to epilepsy. It is believed that the proposed workflow can also be applied to identify genes related to other diseases and deepen our understanding of the mechanisms of these diseases.

Indexed as

AlgorithmsDatabases, GeneticEpilepsyGenetic Association StudiesHumans

Identifiers

PMID28255556
PMCPMC5309434
OpenAlexW2584599619

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.