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Evaluating the informativeness of deep learning annotations for human complex diseases
Deep learning models have shown great promise in predicting regulatory effects from DNA sequence, but their informativeness for human complex diseases is not fully understood. Here, we evaluate genome-wide SNP annotations from two previous deep learning models, DeepSEA and Basenji, by applying strat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499261/ https://www.ncbi.nlm.nih.gov/pubmed/32943643 http://dx.doi.org/10.1038/s41467-020-18515-4 |
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author | Dey, Kushal K. van de Geijn, Bryce Kim, Samuel Sungil Hormozdiari, Farhad Kelley, David R. Price, Alkes L. |
author_facet | Dey, Kushal K. van de Geijn, Bryce Kim, Samuel Sungil Hormozdiari, Farhad Kelley, David R. Price, Alkes L. |
author_sort | Dey, Kushal K. |
collection | PubMed |
description | Deep learning models have shown great promise in predicting regulatory effects from DNA sequence, but their informativeness for human complex diseases is not fully understood. Here, we evaluate genome-wide SNP annotations from two previous deep learning models, DeepSEA and Basenji, by applying stratified LD score regression to 41 diseases and traits (average N = 320K), conditioning on a broad set of coding, conserved and regulatory annotations. We aggregated annotations across all (respectively blood or brain) tissues/cell-types in meta-analyses across all (respectively 11 blood or 8 brain) traits. The annotations were highly enriched for disease heritability, but produced only limited conditionally significant results: non-tissue-specific and brain-specific Basenji-H3K4me3 for all traits and brain traits respectively. We conclude that deep learning models have yet to achieve their full potential to provide considerable unique information for complex disease, and that their conditional informativeness for disease cannot be inferred from their accuracy in predicting regulatory annotations. |
format | Online Article Text |
id | pubmed-7499261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74992612020-10-01 Evaluating the informativeness of deep learning annotations for human complex diseases Dey, Kushal K. van de Geijn, Bryce Kim, Samuel Sungil Hormozdiari, Farhad Kelley, David R. Price, Alkes L. Nat Commun Article Deep learning models have shown great promise in predicting regulatory effects from DNA sequence, but their informativeness for human complex diseases is not fully understood. Here, we evaluate genome-wide SNP annotations from two previous deep learning models, DeepSEA and Basenji, by applying stratified LD score regression to 41 diseases and traits (average N = 320K), conditioning on a broad set of coding, conserved and regulatory annotations. We aggregated annotations across all (respectively blood or brain) tissues/cell-types in meta-analyses across all (respectively 11 blood or 8 brain) traits. The annotations were highly enriched for disease heritability, but produced only limited conditionally significant results: non-tissue-specific and brain-specific Basenji-H3K4me3 for all traits and brain traits respectively. We conclude that deep learning models have yet to achieve their full potential to provide considerable unique information for complex disease, and that their conditional informativeness for disease cannot be inferred from their accuracy in predicting regulatory annotations. Nature Publishing Group UK 2020-09-17 /pmc/articles/PMC7499261/ /pubmed/32943643 http://dx.doi.org/10.1038/s41467-020-18515-4 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dey, Kushal K. van de Geijn, Bryce Kim, Samuel Sungil Hormozdiari, Farhad Kelley, David R. Price, Alkes L. Evaluating the informativeness of deep learning annotations for human complex diseases |
title | Evaluating the informativeness of deep learning annotations for human complex diseases |
title_full | Evaluating the informativeness of deep learning annotations for human complex diseases |
title_fullStr | Evaluating the informativeness of deep learning annotations for human complex diseases |
title_full_unstemmed | Evaluating the informativeness of deep learning annotations for human complex diseases |
title_short | Evaluating the informativeness of deep learning annotations for human complex diseases |
title_sort | evaluating the informativeness of deep learning annotations for human complex diseases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499261/ https://www.ncbi.nlm.nih.gov/pubmed/32943643 http://dx.doi.org/10.1038/s41467-020-18515-4 |
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