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Linear models enable powerful differential activity analysis in massively parallel reporter assays
BACKGROUND: Massively parallel reporter assays (MPRAs) have emerged as a popular means for understanding noncoding variation in a variety of conditions. While a large number of experiments have been described in the literature, analysis typically uses ad-hoc methods. There has been little attention...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417258/ https://www.ncbi.nlm.nih.gov/pubmed/30866806 http://dx.doi.org/10.1186/s12864-019-5556-x |
_version_ | 1783403533007060992 |
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author | Myint, Leslie Avramopoulos, Dimitrios G. Goff, Loyal A. Hansen, Kasper D. |
author_facet | Myint, Leslie Avramopoulos, Dimitrios G. Goff, Loyal A. Hansen, Kasper D. |
author_sort | Myint, Leslie |
collection | PubMed |
description | BACKGROUND: Massively parallel reporter assays (MPRAs) have emerged as a popular means for understanding noncoding variation in a variety of conditions. While a large number of experiments have been described in the literature, analysis typically uses ad-hoc methods. There has been little attention to comparing performance of methods across datasets. RESULTS: We present the mpralm method which we show is calibrated and powerful, by analyzing its performance on multiple MPRA datasets. We show that it outperforms existing statistical methods for analysis of this data type, in the first comprehensive evaluation of statistical methods on several datasets. We investigate theoretical and real-data properties of barcode summarization methods and show an unappreciated impact of summarization method for some datasets. Finally, we use our model to conduct a power analysis for this assay and show substantial improvements in power by performing up to 6 replicates per condition, whereas sequencing depth has smaller impact; we recommend to always use at least 4 replicates. An R package is available from the Bioconductor project. CONCLUSIONS: Together, these results inform recommendations for differential analysis, general group comparisons, and power analysis and will help improve design and analysis of MPRA experiments. |
format | Online Article Text |
id | pubmed-6417258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64172582019-03-25 Linear models enable powerful differential activity analysis in massively parallel reporter assays Myint, Leslie Avramopoulos, Dimitrios G. Goff, Loyal A. Hansen, Kasper D. BMC Genomics Methodology Article BACKGROUND: Massively parallel reporter assays (MPRAs) have emerged as a popular means for understanding noncoding variation in a variety of conditions. While a large number of experiments have been described in the literature, analysis typically uses ad-hoc methods. There has been little attention to comparing performance of methods across datasets. RESULTS: We present the mpralm method which we show is calibrated and powerful, by analyzing its performance on multiple MPRA datasets. We show that it outperforms existing statistical methods for analysis of this data type, in the first comprehensive evaluation of statistical methods on several datasets. We investigate theoretical and real-data properties of barcode summarization methods and show an unappreciated impact of summarization method for some datasets. Finally, we use our model to conduct a power analysis for this assay and show substantial improvements in power by performing up to 6 replicates per condition, whereas sequencing depth has smaller impact; we recommend to always use at least 4 replicates. An R package is available from the Bioconductor project. CONCLUSIONS: Together, these results inform recommendations for differential analysis, general group comparisons, and power analysis and will help improve design and analysis of MPRA experiments. BioMed Central 2019-03-12 /pmc/articles/PMC6417258/ /pubmed/30866806 http://dx.doi.org/10.1186/s12864-019-5556-x Text en © The Author(s) 2019 Open Access This article is distributed under the terms of theCreative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Myint, Leslie Avramopoulos, Dimitrios G. Goff, Loyal A. Hansen, Kasper D. Linear models enable powerful differential activity analysis in massively parallel reporter assays |
title | Linear models enable powerful differential activity analysis in massively parallel reporter assays |
title_full | Linear models enable powerful differential activity analysis in massively parallel reporter assays |
title_fullStr | Linear models enable powerful differential activity analysis in massively parallel reporter assays |
title_full_unstemmed | Linear models enable powerful differential activity analysis in massively parallel reporter assays |
title_short | Linear models enable powerful differential activity analysis in massively parallel reporter assays |
title_sort | linear models enable powerful differential activity analysis in massively parallel reporter assays |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417258/ https://www.ncbi.nlm.nih.gov/pubmed/30866806 http://dx.doi.org/10.1186/s12864-019-5556-x |
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