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Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci
To uncover novel significant association signals (p<5×10(−8)), genome-wide association studies (GWAS) requires increasingly larger sample sizes to overcome statistical correction for multiple testing. As an alternative, we aimed to identify associations among suggestive signals (5 × 10(−8)≤p<5...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815306/ https://www.ncbi.nlm.nih.gov/pubmed/33459256 http://dx.doi.org/10.7554/eLife.62206 |
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author | Hammond, Reza K Pahl, Matthew C Su, Chun Cousminer, Diana L Leonard, Michelle E Lu, Sumei Doege, Claudia A Wagley, Yadav Hodge, Kenyaita M Lasconi, Chiara Johnson, Matthew E Pippin, James A Hankenson, Kurt D Leibel, Rudolph L Chesi, Alessandra Wells, Andrew D Grant, Struan FA |
author_facet | Hammond, Reza K Pahl, Matthew C Su, Chun Cousminer, Diana L Leonard, Michelle E Lu, Sumei Doege, Claudia A Wagley, Yadav Hodge, Kenyaita M Lasconi, Chiara Johnson, Matthew E Pippin, James A Hankenson, Kurt D Leibel, Rudolph L Chesi, Alessandra Wells, Andrew D Grant, Struan FA |
author_sort | Hammond, Reza K |
collection | PubMed |
description | To uncover novel significant association signals (p<5×10(−8)), genome-wide association studies (GWAS) requires increasingly larger sample sizes to overcome statistical correction for multiple testing. As an alternative, we aimed to identify associations among suggestive signals (5 × 10(−8)≤p<5×10(−4)) in increasingly powered GWAS efforts using chromatin accessibility and direct contact with gene promoters as biological constraints. We conducted retrospective analyses of three GIANT BMI GWAS efforts using ATAC-seq and promoter-focused Capture C data from human adipocytes and embryonic stem cell (ESC)-derived hypothalamic-like neurons. This approach, with its extremely low false-positive rate, identified 15 loci at p<5×10(−5) in the 2010 GWAS, of which 13 achieved genome-wide significance by 2018, including at NAV1, MTIF3, and ADCY3. Eighty percent of constrained 2015 loci achieved genome-wide significance in 2018. We observed similar results in waist-to-hip ratio analyses. In conclusion, biological constraints on sub-significant GWAS signals can reveal potentially true-positive loci for further investigation in existing data sets without increasing sample size. |
format | Online Article Text |
id | pubmed-7815306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-78153062021-01-21 Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci Hammond, Reza K Pahl, Matthew C Su, Chun Cousminer, Diana L Leonard, Michelle E Lu, Sumei Doege, Claudia A Wagley, Yadav Hodge, Kenyaita M Lasconi, Chiara Johnson, Matthew E Pippin, James A Hankenson, Kurt D Leibel, Rudolph L Chesi, Alessandra Wells, Andrew D Grant, Struan FA eLife Computational and Systems Biology To uncover novel significant association signals (p<5×10(−8)), genome-wide association studies (GWAS) requires increasingly larger sample sizes to overcome statistical correction for multiple testing. As an alternative, we aimed to identify associations among suggestive signals (5 × 10(−8)≤p<5×10(−4)) in increasingly powered GWAS efforts using chromatin accessibility and direct contact with gene promoters as biological constraints. We conducted retrospective analyses of three GIANT BMI GWAS efforts using ATAC-seq and promoter-focused Capture C data from human adipocytes and embryonic stem cell (ESC)-derived hypothalamic-like neurons. This approach, with its extremely low false-positive rate, identified 15 loci at p<5×10(−5) in the 2010 GWAS, of which 13 achieved genome-wide significance by 2018, including at NAV1, MTIF3, and ADCY3. Eighty percent of constrained 2015 loci achieved genome-wide significance in 2018. We observed similar results in waist-to-hip ratio analyses. In conclusion, biological constraints on sub-significant GWAS signals can reveal potentially true-positive loci for further investigation in existing data sets without increasing sample size. eLife Sciences Publications, Ltd 2021-01-18 /pmc/articles/PMC7815306/ /pubmed/33459256 http://dx.doi.org/10.7554/eLife.62206 Text en © 2021, Hammond et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Hammond, Reza K Pahl, Matthew C Su, Chun Cousminer, Diana L Leonard, Michelle E Lu, Sumei Doege, Claudia A Wagley, Yadav Hodge, Kenyaita M Lasconi, Chiara Johnson, Matthew E Pippin, James A Hankenson, Kurt D Leibel, Rudolph L Chesi, Alessandra Wells, Andrew D Grant, Struan FA Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci |
title | Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci |
title_full | Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci |
title_fullStr | Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci |
title_full_unstemmed | Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci |
title_short | Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci |
title_sort | biological constraints on gwas snps at suggestive significance thresholds reveal additional bmi loci |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815306/ https://www.ncbi.nlm.nih.gov/pubmed/33459256 http://dx.doi.org/10.7554/eLife.62206 |
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