General Commentary ARTICLE
Corrigendum: Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation
- Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada
by Xu, C., Ciampi, A., and Greenwood, C. M. T. (2014). Front. Genet. 5:11. doi: 10.3389/fgene.2014.00011
Regrettably, the Acknowledgments were omitted from the submitted manuscript and are therefore included here in this Corrigendum
The authors were supported by CIHR operating grant MOP-115110 to Celia M. T. Greenwood and Antonio Ciampi, and also by MITACS, the Mathematics of Information Technology and Complex Systems, part of the Canadian Networks of Centres of Excellence program. This study makes use of data generated by the UK10K Consortium, derived from samples from UK10K_COHORTS_TWINSUK (The TwinsUK Cohort) and UK10K_COHORT_ALSPAC (the Avon Longitudinal Study of Parents and Children). A full list of the investigators who contributed to the generation of the data is available from www.UK10K.org. Funding for UK10K was provided by the Wellcome Trust under award WT091310.
Keywords: Acknowledgments, false discovery rates, rare genetic variation, UK10K, region-based tests
Citation: Greenwood CMT (2014) Corrigendum: Exploring the potential benefits of stratified false discovery rates for region-based testing of association with rare genetic variation. Front. Genet. 5:61. doi: 10.3389/fgene.2014.00061
Received: 07 March 2014; Accepted: 11 March 2014;
Published online: 26 March 2014.
Edited and reviewed by: Joanna Biernacka, Mayo Clinic, USA
Copyright © 2014 Greenwood. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.