ArticleBioinformatics (Oxford, England)2016
A network-driven approach for genome-wide association mapping.
Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Addressing noise in co-expression network construction.Briefings in bioinformatics · 2022Review
- Using expression quantitative trait loci data and graph-embedded neural networks to uncover genotype-phenotype interactions.Frontiers in genetics · 2022Article
- Linking genotype to phenotype in multi-omics data of small sample.BMC genomics · 2021Article
- A Network-guided Association Mapping Approach from DNA Methylation to Disease.Scientific reports · 2019Article
- Ensembles of Lasso Screening Rules.IEEE transactions on pattern analysis and machine intelligence · 2018Article
- Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls.Scientific reports · 2018Article
- PlasFlow: predicting plasmid sequences in metagenomic data using genome signatures.Nucleic acids research · 2018Article
- Backward genotype-transcript-phenotype association mapping.Methods (San Diego, Calif.) · 2017Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
motivationIt remains a challenge to detect associations between genotypes and phenotypes because of insufficient sample sizes and complex underlying mechanisms involved in associations. Fortunately, it is becoming more feasible to obtain gene expression data in addition to genotypes and phenotypes, giving us new opportunities to detect true genotype-phenotype associations while unveiling their association mechanisms.
resultsIn this article, we propose a novel method, NETAM, that accurately detects associations between SNPs and phenotypes, as well as gene traits involved in such associations. We take a network-driven approach: NETAM first constructs an association network, where nodes represent SNPs, gene traits or phenotypes, and edges represent the strength of association between two nodes. NETAM assigns a score to each path from an SNP to a phenotype, and then identifies significant paths based on the scores. In our simulation study, we show that NETAM finds significantly more phenotype-associated SNPs than traditional genotype-phenotype association analysis under false positive control, taking advantage of gene expression data. Furthermore, we applied NETAM on late-onset Alzheimer's disease data and identified 477 significant path associations, among which we analyzed paths related to beta-amyloid, estrogen, and nicotine pathways. We also provide hypothetical biological pathways to explain our findings. AVAILABILITY AND IMPLEMENTATION: Software is available at http://www.sailing.cs.cmu.edu/ CONTACT: : epxing@cs.cmu.edu.
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Registered trials
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.