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Power calculator for detecting allelic imbalance using hierarchical Bayesian model
OBJECTIVE: Allelic imbalance (AI) is the differential expression of the two alleles in a diploid. AI can vary between tissues, treatments, and environments. Methods for testing AI exist, but methods are needed to estimate type I error and power for detecting AI and difference of AI between condition...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626927/ https://www.ncbi.nlm.nih.gov/pubmed/34838135 http://dx.doi.org/10.1186/s13104-021-05851-x |
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author | Sherbina, Katrina León-Novelo, Luis G. Nuzhdin, Sergey V. McIntyre, Lauren M. Marroni, Fabio |
author_facet | Sherbina, Katrina León-Novelo, Luis G. Nuzhdin, Sergey V. McIntyre, Lauren M. Marroni, Fabio |
author_sort | Sherbina, Katrina |
collection | PubMed |
description | OBJECTIVE: Allelic imbalance (AI) is the differential expression of the two alleles in a diploid. AI can vary between tissues, treatments, and environments. Methods for testing AI exist, but methods are needed to estimate type I error and power for detecting AI and difference of AI between conditions. As the costs of the technology plummet, what is more important: reads or replicates? RESULTS: We find that a minimum of 2400, 480, and 240 allele specific reads divided equally among 12, 5, and 3 replicates is needed to detect a 10, 20, and 30%, respectively, deviation from allelic balance in a condition with power > 80%. A minimum of 960 and 240 allele specific reads divided equally among 8 replicates is needed to detect a 20 or 30% difference in AI between conditions with comparable power. Higher numbers of replicates increase power more than adding coverage without affecting type I error. We provide a Python package that enables simulation of AI scenarios and enables individuals to estimate type I error and power in detecting AI and differences in AI between conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-021-05851-x. |
format | Online Article Text |
id | pubmed-8626927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86269272021-11-29 Power calculator for detecting allelic imbalance using hierarchical Bayesian model Sherbina, Katrina León-Novelo, Luis G. Nuzhdin, Sergey V. McIntyre, Lauren M. Marroni, Fabio BMC Res Notes Research Note OBJECTIVE: Allelic imbalance (AI) is the differential expression of the two alleles in a diploid. AI can vary between tissues, treatments, and environments. Methods for testing AI exist, but methods are needed to estimate type I error and power for detecting AI and difference of AI between conditions. As the costs of the technology plummet, what is more important: reads or replicates? RESULTS: We find that a minimum of 2400, 480, and 240 allele specific reads divided equally among 12, 5, and 3 replicates is needed to detect a 10, 20, and 30%, respectively, deviation from allelic balance in a condition with power > 80%. A minimum of 960 and 240 allele specific reads divided equally among 8 replicates is needed to detect a 20 or 30% difference in AI between conditions with comparable power. Higher numbers of replicates increase power more than adding coverage without affecting type I error. We provide a Python package that enables simulation of AI scenarios and enables individuals to estimate type I error and power in detecting AI and differences in AI between conditions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-021-05851-x. BioMed Central 2021-11-27 /pmc/articles/PMC8626927/ /pubmed/34838135 http://dx.doi.org/10.1186/s13104-021-05851-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Note Sherbina, Katrina León-Novelo, Luis G. Nuzhdin, Sergey V. McIntyre, Lauren M. Marroni, Fabio Power calculator for detecting allelic imbalance using hierarchical Bayesian model |
title | Power calculator for detecting allelic imbalance using hierarchical Bayesian model |
title_full | Power calculator for detecting allelic imbalance using hierarchical Bayesian model |
title_fullStr | Power calculator for detecting allelic imbalance using hierarchical Bayesian model |
title_full_unstemmed | Power calculator for detecting allelic imbalance using hierarchical Bayesian model |
title_short | Power calculator for detecting allelic imbalance using hierarchical Bayesian model |
title_sort | power calculator for detecting allelic imbalance using hierarchical bayesian model |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626927/ https://www.ncbi.nlm.nih.gov/pubmed/34838135 http://dx.doi.org/10.1186/s13104-021-05851-x |
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