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Depositordc.contributorBoutin, Thibaud
Funderdc.contributor.otherMRC - Medical Research Councilen_UK
Spatial Coveragedc.coverage.spatialLondonen_UK
Spatial Coveragedc.coverage.spatialScotlanden_UK
Spatial Coveragedc.coverage.spatialUKen
Spatial Coveragedc.coverage.spatialUNITED KINGDOMen
Data Creatordc.creatorBoutin, Thibaud
Data Creatordc.creatorVitart, Veronique
Date Accessioneddc.date.accessioned2019-11-20T14:36:53Z
Citationdc.identifier.citationBoutin, Thibaud; Vitart, Veronique. (2019). Insights into the genetic basis of retinal detachment, [dataset]. MRC Human Genetics Unit IGMM. University of Edinburgh.en
Persistent Identifierdc.identifier.urihttp://hdl.handle.net/10283/3511
Persistent Identifierdc.identifier.urihttps://doi.org/10.7488/ds/2712
Dataset Description (abstract)dc.description.abstractDataset of genome-wide association meta-analysis summary statistics associated with the publication “Insights into the genetic basis of retinal detachment” available as a preprint at BiorXiv: doi: https://doi.org/10.1101/581165. If you use this dataset, please cite the manuscript in order to fairly acknowledge the contribution of all participating studies and their sponsors.en_UK
Dataset Description (TOC)dc.description.tableofcontentsThis dataset encloses a single tab-delimited compressed file rd_meta.tbl.gz containing the individual summary statistic of over 7.5 million SNPs imputed with the Haplotype Reference Consortium (HRCr1-1). These results were obtained by conducting an inverse variance weighted meta-analysis of the effect of the genome-wide association studies of retinal detachment case-control sets from the UK Biobank or clinically ascertained as described in the manuscript. File header description: MarkerName is the unique variant name chromosome_position; CHR the chromosome number; BP is the physical location (bp) based on the genome build GRCh37; Allele1 is the effect allele for which the effect of retinal detachment has been reported (Effect); Allele2 the alternate allele; Freq1 is the mean frequency of the effect allele (Allele1); Effect is the meta-analysis effect size; StdErr is the standard error of the effect; Pvalue the P-value of the test; ID the rsid (dbSNP).en_UK
Languagedc.language.isoengen_UK
Publisherdc.publisherMRC Human Genetics Unit IGMM. University of Edinburghen_UK
Relation (Is Referenced By)dc.relation.isreferencedbyhttps://doi.org/10.1101/581165
Rightsdc.rightsCreative Commons Attribution 4.0 International Public Licenseen
Subjectdc.subjectretinal detachmenten_UK
Subjectdc.subjectGWASen_UK
Subjectdc.subjectcase controlen_UK
Subjectdc.subjectclinicalen_UK
Subjectdc.subjectuk biobanken_UK
Subjectdc.subjectfine-mappingen_UK
Subjectdc.subjectgenetic correlationen_UK
Subjectdc.subjectshared aetiologyen_UK
Subjectdc.subjectcase ascertainmenten_UK
Subject Classificationdc.subject.classificationBiological Sciences::Human Geneticsen_UK
Titledc.titleInsights into the genetic basis of retinal detachmenten_UK
Typedc.typedataseten_UK
Embargo Datedc.date.embargo2020-01-15


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