Evidence map›Paper›PMID 30295737›Full record

ArticleBioinformatics (Oxford, England)2019

CoMM: a collaborative mixed model to dissecting genetic contributions to complex traits by leveraging regulatory information.

Can Yang, Xiang Wan, Xinyi Lin, Mengjie Chen, Xiang Zhou, Jin Liu

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Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

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3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

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  18. CoMM-SFrontiers in genetics · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Can YangDepartment of Mathematics, Hong Kong University of Science and Technology, Hong Kong, China.
Xiang WanShenzhen Research Institute of Big Data, Shenzhen, China.
Xinyi LinCentre for Quantitative Medicine, Program in Health Services and Systems Research, Duke-NUS Medical School, Singapore.
Mengjie ChenDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Xiang ZhouDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
Jin LiuCentre for Quantitative Medicine, Program in Health Services and Systems Research, Duke-NUS Medical School, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationGenome-wide association studies (GWASs) have been successful in identifying many genetic variants associated with complex traits. However, the mechanistic links between these variants and complex traits remain elusive. A scientific hypothesis is that genetic variants influence complex traits at the organismal level via affecting cellular traits, such as regulating gene expression and altering protein abundance. Although earlier works have already presented some scientific insights about this hypothesis and their findings are very promising, statistical methods that effectively harness multilayered data (e.g. genetic variants, cellular traits and organismal traits) on a large scale for functional and mechanistic exploration are highly demanding.

resultsIn this study, we propose a collaborative mixed model (CoMM) to investigate the mechanistic role of associated variants in complex traits. The key idea is built upon the emerging scientific evidence that genetic effects at the cellular level are much stronger than those at the organismal level. Briefly, CoMM combines two models: the first model relating gene expression with genotype and the second model relating phenotype with predicted gene expression using the first model. The two models are fitted jointly in CoMM, such that the uncertainty in predicting gene expression has been fully accounted. To demonstrate the advantages of CoMM over existing methods, we conducted extensive simulation studies, and also applied CoMM to analyze 25 traits in NFBC1966 and Genetic Epidemiology Research on Aging (GERA) studies by integrating transcriptome information from the Genetic European in Health and Disease (GEUVADIS) Project. The results indicate that by leveraging regulatory information, CoMM can effectively improve the power of prioritizing risk variants. Regarding the computational efficiency, CoMM can complete the analysis of NFBC1966 dataset and GERA datasets in 2 and 18 min, respectively. AVAILABILITY AND IMPLEMENTATION: The developed R package is available at https://github.com/gordonliu810822/CoMM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

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Multifactorial InheritanceGenome-Wide Association StudyGenotypePhenotypeSoftware

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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.