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

Summary: 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 (aver...

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Publicat a:Bioinformatics
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2015
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Applications Notes
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4673976/
https://ncbi.nlm.nih.gov/pubmed/26315906
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv491
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