An interactive genome browser of association results from the UK10K cohorts project

High-throughput sequencing technologies survey genetic variation at genome scale and are increasingly used to study the contribution of rare and low-frequency genetic variants to human traits. As part of the Cohorts arm of the UK10K project, genetic variants called from low-read depth (average 7×) w...

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Veröffentlicht in:Bioinformatics (Oxford, England) England), 2015-12, Vol.31 (24), p.4029-4031
Hauptverfasser: Geihs, Matthias, Yan, Ying, Walter, Klaudia, Huang, Jie, Memari, Yasin, Min, Josine L, Mead, Daniel, Hubbard, Tim J, Timpson, Nicholas J, Down, Thomas A, Soranzo, Nicole
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Sprache:eng
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Zusammenfassung:High-throughput sequencing technologies survey genetic variation at genome scale and are increasingly used to study the contribution of rare and low-frequency genetic variants to human traits. As part of the Cohorts arm of the UK10K project, genetic variants called from low-read depth (average 7×) whole genome sequencing of 3621 cohort individuals were analysed for statistical associations with 64 different phenotypic traits of biomedical importance. Here, we describe a novel genome browser based on the Biodalliance platform developed to provide interactive access to the association results of the project. The browser is available at http://www.uk10k.org/dalliance.html. Source code for the Biodalliance platform is available under a BSD license from http://github.com/dasmoth/dalliance, and for the LD-display plugin and backend from http://github.com/dasmoth/ldserv.
ISSN:1367-4803
1367-4811
DOI:10.1093/bioinformatics/btv491