Regrettably, the Acknowledgments were omitted from the submitted manuscript and are therefore included here in this Corrigendum
Statements
Acknowledgments
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.
Summary
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
26 March 2014
Volume
5 - 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.
*Correspondence: celia.greenwood@mcgill.ca
This article was submitted to Statistical Genetics and Methodology, a section of the journal Frontiers in Genetics.
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