# Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis

## Author(s): Yang, Fan; Wang, Jiebiao; GTEx Consortium; Pierce, Brandon L; Chen, Lin S

To refer to this page use: http://arks.princeton.edu/ark:/88435/pr12257
DC FieldValueLanguage
dc.contributor.authorYang, Fan-
dc.contributor.authorWang, Jiebiao-
dc.contributor.authorGTEx Consortium-
dc.contributor.authorPierce, Brandon L-
dc.contributor.authorChen, Lin S-
dc.date.accessioned2021-10-08T19:49:18Z-
dc.date.available2021-10-08T19:49:18Z-
dc.date.issued2017en_US
dc.identifier.citationYang, Fan, Jiebiao Wang, Brandon L. Pierce, Lin S. Chen, François Aguet, Kristin G. Ardlie, Beryl B. Cummings et al. "Identifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysis." Genome Research 27, no. 11 (2017): pp. 1859-1871. doi:10.1101/gr.216754.116en_US
dc.identifier.issn1088-9051-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr12257-
dc.description.abstractThe impact of inherited genetic variation on gene expression in humans is well-established. The majority of known expression quantitative trait loci (eQTLs) impact expression of local genes (cis-eQTLs). More research is needed to identify effects of genetic variation on distant genes (trans-eQTLs) and understand their biological mechanisms. One common trans-eQTLs mechanism is “mediation” by a local (cis) transcript. Thus, mediation analysis can be applied to genome-wide SNP and expression data in order to identify transcripts that are “cis-mediators” of trans-eQTLs, including those “cis-hubs” involved in regulation of many trans-genes. Identifying such mediators helps us understand regulatory networks and suggests biological mechanisms underlying trans-eQTLs, both of which are relevant for understanding susceptibility to complex diseases. The multitissue expression data from the Genotype-Tissue Expression (GTEx) program provides a unique opportunity to study cis-mediation across human tissue types. However, the presence of complex hidden confounding effects in biological systems can make mediation analyses challenging and prone to confounding bias, particularly when conducted among diverse samples. To address this problem, we propose a new method: Genomic Mediation analysis with Adaptive Confounding adjustment (GMAC). It enables the search of a very large pool of variables, and adaptively selects potential confounding variables for each mediation test. Analyses of simulated data and GTEx data demonstrate that the adaptive selection of confounders by GMAC improves the power and precision of mediation analysis. Application of GMAC to GTEx data provides new insights into the observed patterns of cis-hubs and trans-eQTL regulation across tissue types.en_US
dc.format.extent1859 - 1871en_US
dc.languageengen_US
dc.language.isoen_USen_US
dc.relation.ispartofGenome Researchen_US
dc.rightsFinal published version. Article is made available in OAR by the publisher's permission or policy.en_US
dc.titleIdentifying cis-mediators for trans-eQTLs across many human tissues using genomic mediation analysisen_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1101/gr.216754.116-
dc.identifier.eissn1549-5469-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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