Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/172139
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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.identifier.issn0007-0920-
dc.identifier.urihttp://hdl.handle.net/2445/172139-
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.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.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-
dc.identifier.idgrec685290-
dc.date.updated2020-11-17T14:02:59Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid30283144-
Appears in Collections:Articles publicats en revistes (Ciències Clíniques)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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