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Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis
The diagnostic yield of exome and genome sequencing remains low (8–70%), due to incomplete knowledge on the genes that cause disease. To improve this, we use RNA-seq data from 31,499 samples to predict which genes cause specific disease phenotypes, and develop GeneNetwork Assisted Diagnostic Optimiz...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599066/ https://www.ncbi.nlm.nih.gov/pubmed/31253775 http://dx.doi.org/10.1038/s41467-019-10649-4 |
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author | Deelen, Patrick van Dam, Sipko Herkert, Johanna C. Karjalainen, Juha M. Brugge, Harm Abbott, Kristin M. van Diemen, Cleo C. van der Zwaag, Paul A. Gerkes, Erica H. Zonneveld-Huijssoon, Evelien Boer-Bergsma, Jelkje J. Folkertsma, Pytrik Gillett, Tessa van der Velde, K. Joeri Kanninga, Roan van den Akker, Peter C. Jan, Sabrina Z. Hoorntje, Edgar T. te Rijdt, Wouter P. Vos, Yvonne J. Jongbloed, Jan D. H. van Ravenswaaij-Arts, Conny M. A. Sinke, Richard Sikkema-Raddatz, Birgit Kerstjens-Frederikse, Wilhelmina S. Swertz, Morris A. Franke, Lude |
author_facet | Deelen, Patrick van Dam, Sipko Herkert, Johanna C. Karjalainen, Juha M. Brugge, Harm Abbott, Kristin M. van Diemen, Cleo C. van der Zwaag, Paul A. Gerkes, Erica H. Zonneveld-Huijssoon, Evelien Boer-Bergsma, Jelkje J. Folkertsma, Pytrik Gillett, Tessa van der Velde, K. Joeri Kanninga, Roan van den Akker, Peter C. Jan, Sabrina Z. Hoorntje, Edgar T. te Rijdt, Wouter P. Vos, Yvonne J. Jongbloed, Jan D. H. van Ravenswaaij-Arts, Conny M. A. Sinke, Richard Sikkema-Raddatz, Birgit Kerstjens-Frederikse, Wilhelmina S. Swertz, Morris A. Franke, Lude |
author_sort | Deelen, Patrick |
collection | PubMed |
description | The diagnostic yield of exome and genome sequencing remains low (8–70%), due to incomplete knowledge on the genes that cause disease. To improve this, we use RNA-seq data from 31,499 samples to predict which genes cause specific disease phenotypes, and develop GeneNetwork Assisted Diagnostic Optimization (GADO). We show that this unbiased method, which does not rely upon specific knowledge on individual genes, is effective in both identifying previously unknown disease gene associations, and flagging genes that have previously been incorrectly implicated in disease. GADO can be run on www.genenetwork.nl by supplying HPO-terms and a list of genes that contain candidate variants. Finally, applying GADO to a cohort of 61 patients for whom exome-sequencing analysis had not resulted in a genetic diagnosis, yields likely causative genes for ten cases. |
format | Online Article Text |
id | pubmed-6599066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65990662019-07-01 Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis Deelen, Patrick van Dam, Sipko Herkert, Johanna C. Karjalainen, Juha M. Brugge, Harm Abbott, Kristin M. van Diemen, Cleo C. van der Zwaag, Paul A. Gerkes, Erica H. Zonneveld-Huijssoon, Evelien Boer-Bergsma, Jelkje J. Folkertsma, Pytrik Gillett, Tessa van der Velde, K. Joeri Kanninga, Roan van den Akker, Peter C. Jan, Sabrina Z. Hoorntje, Edgar T. te Rijdt, Wouter P. Vos, Yvonne J. Jongbloed, Jan D. H. van Ravenswaaij-Arts, Conny M. A. Sinke, Richard Sikkema-Raddatz, Birgit Kerstjens-Frederikse, Wilhelmina S. Swertz, Morris A. Franke, Lude Nat Commun Article The diagnostic yield of exome and genome sequencing remains low (8–70%), due to incomplete knowledge on the genes that cause disease. To improve this, we use RNA-seq data from 31,499 samples to predict which genes cause specific disease phenotypes, and develop GeneNetwork Assisted Diagnostic Optimization (GADO). We show that this unbiased method, which does not rely upon specific knowledge on individual genes, is effective in both identifying previously unknown disease gene associations, and flagging genes that have previously been incorrectly implicated in disease. GADO can be run on www.genenetwork.nl by supplying HPO-terms and a list of genes that contain candidate variants. Finally, applying GADO to a cohort of 61 patients for whom exome-sequencing analysis had not resulted in a genetic diagnosis, yields likely causative genes for ten cases. Nature Publishing Group UK 2019-06-28 /pmc/articles/PMC6599066/ /pubmed/31253775 http://dx.doi.org/10.1038/s41467-019-10649-4 Text en © The Author(s) 2019 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 Deelen, Patrick van Dam, Sipko Herkert, Johanna C. Karjalainen, Juha M. Brugge, Harm Abbott, Kristin M. van Diemen, Cleo C. van der Zwaag, Paul A. Gerkes, Erica H. Zonneveld-Huijssoon, Evelien Boer-Bergsma, Jelkje J. Folkertsma, Pytrik Gillett, Tessa van der Velde, K. Joeri Kanninga, Roan van den Akker, Peter C. Jan, Sabrina Z. Hoorntje, Edgar T. te Rijdt, Wouter P. Vos, Yvonne J. Jongbloed, Jan D. H. van Ravenswaaij-Arts, Conny M. A. Sinke, Richard Sikkema-Raddatz, Birgit Kerstjens-Frederikse, Wilhelmina S. Swertz, Morris A. Franke, Lude Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis |
title | Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis |
title_full | Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis |
title_fullStr | Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis |
title_full_unstemmed | Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis |
title_short | Improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis |
title_sort | improving the diagnostic yield of exome- sequencing by predicting gene–phenotype associations using large-scale gene expression analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599066/ https://www.ncbi.nlm.nih.gov/pubmed/31253775 http://dx.doi.org/10.1038/s41467-019-10649-4 |
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