Colon-specific eQTL analysis to inform on functional SNPs

dc.contributor.authorMoreno Aguado, Víctor
dc.contributor.authorAlonso Aguado, Maria Henar
dc.contributor.authorClosa, Adrià
dc.contributor.authorVallès, Xavier
dc.contributor.authorDíez Villanueva, Anna
dc.contributor.authorValle Velasco, Laura
dc.contributor.authorCastellví Bel, Sergi
dc.contributor.authorSanz Pamplona, Rebeca
dc.contributor.authorLópez Dóriga Guerra, Adriana
dc.contributor.authorCordero Romera, David
dc.contributor.authorSolé Acha, Xavier
dc.date.accessioned2020-11-17T14:02:58Z
dc.date.available2020-11-17T14:02:58Z
dc.date.issued2018-10-01
dc.date.updated2020-11-17T14:02:59Z
dc.description.abstractBACKGROUND: Genome-wide association studies on colorectal cancer have identified more than 60 susceptibility loci, but for most of them there is no clear knowledge of functionality or the underlying gene responsible for the risk modification. Expression quantitative trail loci (eQTL) may provide functional information for such single nucleotide polymorphisms (SNPs). METHODS: We have performed detailed eQTL analysis specific for colon tissue on a series of 97 colon tumours, their paired adjacent normal mucosa and 47 colon mucosa samples donated by healthy individuals. R package MatrixEQTL was used to search for genome-wide cis-eQTL and trans-eQTL fitting linear models adjusted for age, gender and tissue type to rank transformed expression data. RESULTS: The cis-eQTL analyses has revealed 29,073 SNP-gene associations with permutation-adjusted P-values < 0.01. These correspond to 363 unique genes. The trans-eQTL analysis identified 10,665 significant SNP-gene associations, most of them in the same chromosome, further than 1 Mb of the gene. We provide a web tool to search for specific SNPs or genes. The tool calculates Pearson or Spearman correlation, and allows to select tissue type for analysis. Data and plots can be exported. CONCLUSIONS: This resource should be useful to prioritise SNPs for further functional studies and to identify relevant genes behind identified loci.
dc.format.extent7 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec685290
dc.identifier.issn0007-0920
dc.identifier.pmid30283144
dc.identifier.urihttps://hdl.handle.net/2445/172139
dc.language.isoeng
dc.publisherCancer Research UK
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41416-018-0018-9
dc.relation.ispartofBritish Journal of Cancer, 2018, vol. 119, num. 8, p. 971-977
dc.relation.urihttps://doi.org/10.1038/s41416-018-0018-9
dc.rightscc by-nc-sa (c) Moreno Aguado et al., 2018
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/es/
dc.sourceArticles publicats en revistes (Ciències Clíniques)
dc.subject.classificationCàncer colorectal
dc.subject.classificationGenètica
dc.subject.otherColorectal cancer
dc.subject.otherGenetics
dc.titleColon-specific eQTL analysis to inform on functional SNPs
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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