Evidence map›Paper›PMID 35205221›Full record

ArticleGenes2022

Research on Frequent Itemset Mining of Imaging Genetics GWAS in Alzheimer's Disease.

Hong Liang, Luolong Cao, Yue Gao, Haoran Luo, Xianglian Meng, Ying Wang, Jin Li, Wenjie Liu

Open access · goldAbstract read
In one paragraph

Article in Genes, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Hong LiangCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, Harbin 150001, China.ORCID 0000-0002-2590-7210
Luolong CaoCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, Harbin 150001, China.
Yue GaoCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, Harbin 150001, China.
Haoran LuoCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, Harbin 150001, China.
Xianglian MengSchool of Computer Information and Engineering, Changzhou Institute of Technology, Changzhou 213032, China.
Ying WangSchool of Computer Science and Engineering, Changshu Institute of Technology, Changshu 215500, China.
Jin LiCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, Harbin 150001, China.
Wenjie LiuCollege of Intelligent Systems Science and Engineering, Harbin Engineering University, Harbin 150001, China.ORCID 0000-0003-3220-5820
Harbin Engineering University · CNChangzhou Institute of Technology · CNSuzhou University of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As an efficient method, genome-wide association study (GWAS) is used to identify the association between genetic variation and pathological phenotypes, and many significant genetic variations founded by GWAS are closely associated with human diseases. However, it is not enough to mine only a single marker effect variation on complex biological phenotypes. Mining highly correlated single nucleotide polymorphisms (SNP) is more meaningful for the study of Alzheimer's disease (AD). In this paper, we used two frequent pattern mining (FPM) framework, the FP-Growth and Eclat algorithms, to analyze the GWAS results of functional magnetic resonance imaging (fMRI) phenotypes. Moreover, we applied the definition of confidence to FP-Growth and Eclat to enhance the FPM framework. By calculating the conditional probability of identified SNPs, we obtained the corresponding association rules to provide support confidence between these important SNPs. The resulting SNPs showed close correlation with hippocampus, memory, and AD. The experimental results also demonstrate that our framework is effective in identifying SNPs and provide candidate SNPs for further research.

Indexed as

Alzheimer DiseaseGenome-Wide Association StudyHumansMagnetic Resonance ImagingPhenotypePolymorphism, Single NucleotideAlzheimer’s diseaseassociation rulesEclatFIFPMvGWAS

Identifiers

PMID35205221
PMCPMC8871801
OpenAlexW4206232889

What OpenQuestion 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 OpenQuestion graph.