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Analisis eQTL Multi-Omik×Kajian Persatuan Seluruh Genom (GWAS)×
BidangBioinformatikBioinformatik
KeluargaProcess / pipelineProcess / pipeline
Tahun asal2010s–present (foundational eQTL work: ~2007; multi-omics integration: ~2013–2017)2005–2007
PengasasGTEx Consortium and multi-omics integration pioneers (Nica & Dermitzakis, 2013; GTEx Consortium, 2015–2020)Klein et al. (age-related macular degeneration GWAS, 2005); landmark scale: Wellcome Trust Case Control Consortium (2007)
JenisIntegrative genomic association analysisObservational genomic association study
Sumber perintisGTEx Consortium. (2017). Genetic effects on gene expression across human tissues. Nature, 550(7675), 204–213. link ↗Wellcome Trust Case Control Consortium. (2007). Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature, 447(7145), 661–678. link ↗
Aliasmulti-omics molQTL, multi-layer eQTL, integrated eQTL analysis, xQTL multi-omicsGWAS, genome-wide association analysis, whole-genome association study, WGAS
Berkaitan66
RingkasanMulti-omics eQTL analysis maps genetic variants (SNPs or structural variants) to molecular phenotypes simultaneously across multiple omics layers — transcriptome, epigenome, proteome, and metabolome — in the same cohort. By linking genotype to gene expression and then tracing those effects through downstream molecular layers, the approach reveals how genetic variation propagates through the molecular machinery of a cell, yielding mechanistic insight that no single-omics eQTL study can provide.A genome-wide association study (GWAS) systematically tests hundreds of thousands to millions of single-nucleotide polymorphisms (SNPs) across the human genome for statistical association with a trait or disease. By comparing allele frequencies between cases and controls — or by regressing SNP genotypes on a quantitative phenotype — GWAS identifies genomic loci that harbor common genetic variants contributing to complex traits. Since its large-scale debut in 2007, GWAS has catalogued thousands of robust disease–variant associations across virtually every common human condition.
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ScholarGateBandingkan kaedah: Multi-omics eQTL analysis · Genome-wide association study. Dicapai 2026-06-18 daripada https://scholargate.app/ms/compare