Evidence map›Paper›PMID 33931008›Full record

ArticleBMC bioinformatics2021

Genome-wide variant-based study of genetic effects with the largest neuroanatomic coverage.

Jin Li, Wenjie Liu, Huang Li, Feng Chen, Haoran Luo, Peihua Bao, Yanzhao Li, Hailong Jiang, Yue Gao, Hong Liang and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2021. 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
–field-weighted citation impact, top 96% 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, 0 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

11 authors at 2 institutions in 2 countries.

Jin LiCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Wenjie LiuCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Huang LiComputer and Information Science, IUPUI, 723 W Michigan St, Indianapolis, IN, 46202, USA.
Feng ChenCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Haoran LuoCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Peihua BaoCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Yanzhao LiCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Hailong JiangCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Yue GaoCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.
Hong LiangCollege of Automation, Harbin Engineering University, NO. 145 Nantong Street, Nangang District, Harbin, 150001, China.ORCID http://orcid.org/0000-0002-2590-7210
Shiaofen FangComputer and Information Science, IUPUI, 723 W Michigan St, Indianapolis, IN, 46202, USA. lh@hrbeu.edu.cn.
Harbin Engineering University · CNIndiana University – Purdue University Indianapolis · US

Funding

China Scholarship Fund 201806680080Fundamental Research Funds for the Central Universities 3072020CF0402MOE (Ministry of Education in China) Project of Humanities and Social Sciences 19YJCZH120National Natural Science Foundation of China 61773134National Natural Science Foundation of China 61803117National Natural Science Foundation of China 61901063Natural Science Foundation of Heilongjiang Province of China QC2018080Natural Science Foundation of Heilongjiang Province of China YQ2019F003
6 · The paper itself

Abstract

backgroundBrain image genetics provides enormous opportunities for examining the effects of genetic variations on the brain. Many studies have shown that the structure, function, and abnormality (e.g., those related to Alzheimer's disease) of the brain are heritable. However, which genetic variations contribute to these phenotypic changes is not completely clear. Advances in neuroimaging and genetics have led us to obtain detailed brain anatomy and genome-wide information. These data offer us new opportunities to identify genetic variations such as single nucleotide polymorphisms (SNPs) that affect brain structure. In this paper, we perform a genome-wide variant-based study, and aim to identify top SNPs or SNP sets which have genetic effects with the largest neuroanotomic coverage at both voxel and region-of-interest (ROI) levels. Based on the voxelwise genome-wide association study (GWAS) results, we used the exhaustive search to find the top SNPs or SNP sets that have the largest voxel-based or ROI-based neuroanatomic coverage. For SNP sets with >2 SNPs, we proposed an efficient genetic algorithm to identify top SNP sets that can cover all ROIs or a specific ROI.

resultsWe identified an ensemble of top SNPs, SNP-pairs and SNP-sets, whose effects have the largest neuroanatomic coverage. Experimental results on real imaging genetics data show that the proposed genetic algorithm is superior to the exhaustive search in terms of computational time for identifying top SNP-sets.

conclusionsWe proposed and applied an informatics strategy to identify top SNPs, SNP-pairs and SNP-sets that have genetic effects with the largest neuroanatomic coverage. The proposed genetic algorithm offers an efficient solution to accomplish the task, especially for identifying top SNP-sets.

Indexed as

Alzheimer DiseaseGenome-Wide Association StudyGenomeHumansNeuroimagingPolymorphism, Single NucleotideBrainGenetic algorithmGWASImage geneticsSNPVoxel

Identifiers

PMID33931008
PMCPMC8086096
OpenAlexW3157372227

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.