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| Hálózatalapú eQTL analízis× | Bayes-féle eQTL analízis× | |
|---|---|---|
| Tudományterület | Bioinformatika | Bioinformatika |
| Módszercsalád | Process / pipeline | Process / pipeline |
| Keletkezés éve≠ | 2008–2013 (network-integrated extensions of eQTL mapping) | 2000s–2010s |
| Megalkotó≠ | Multiple groups; foundational eQTL work by Cheung et al. (2005) and Stranger et al. (2007); network integration extended by Zhu et al. (2008) and others | Matthew Stephens, David J. Balding (Bayesian framework for genetic association); extended by multiple groups for eQTL context |
| Típus≠ | Statistical genomics / network analysis pipeline | Probabilistic genomic association method |
| Alapmű≠ | Skinner, M. E., Uzilov, A. V., Stein, L. D., Mungall, C. J., & Holmes, I. H. (2009). JBrowse: a next-generation genome browser. Genome Research, 19(9), 1630–1638. link ↗ | Stephens, M., & Balding, D. J. (2009). Bayesian statistical methods for genetic association studies. Nature Reviews Genetics, 10(10), 681–690. DOI ↗ |
| Alternatív nevek | network eQTL, network-integrated eQTL mapping, graph-based eQTL analysis, eQTL network analysis | Bayesian eQTL mapping, probabilistic eQTL analysis, Bayesian QTL mapping for gene expression, eQTL fine-mapping |
| Kapcsolódó≠ | 5 | 6 |
| Összefoglaló≠ | Network-based eQTL analysis extends classical eQTL mapping by embedding genetic variant-to-expression associations within gene regulatory or protein interaction networks. Rather than treating each SNP-gene pair independently, this approach leverages network topology — such as co-expression modules or known pathway structures — to improve statistical power, reduce multiple testing burden, and reveal how genetic variants perturb entire regulatory programs rather than isolated transcripts. | Bayesian eQTL analysis identifies genetic variants (eQTLs) that regulate gene expression by combining genotype and RNA-seq data within a probabilistic framework. Unlike frequentist approaches that rely on p-value thresholds, the Bayesian formulation produces posterior probabilities of association, enabling principled fine-mapping of causal variants and coherent uncertainty quantification across thousands of gene-SNP pairs simultaneously. |
| ScholarGateAdatkészlet ↗ |
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