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Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes
Although clinical and laboratory data have long been used to guide medical practice, this information is rarely integrated with multi-omic data to identify endotypes. We present Merged Affinity Network Association Clustering (MANAclust), a coding-free, automated pipeline enabling integration of cate...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195153/ https://www.ncbi.nlm.nih.gov/pubmed/33852839 http://dx.doi.org/10.1016/j.celrep.2021.108975 |
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author | Tyler, Scott R. Chun, Yoojin Ribeiro, Victoria M. Grishina, Galina Grishin, Alexander Hoffman, Gabriel E. Do, Anh N. Bunyavanich, Supinda |
author_facet | Tyler, Scott R. Chun, Yoojin Ribeiro, Victoria M. Grishina, Galina Grishin, Alexander Hoffman, Gabriel E. Do, Anh N. Bunyavanich, Supinda |
author_sort | Tyler, Scott R. |
collection | PubMed |
description | Although clinical and laboratory data have long been used to guide medical practice, this information is rarely integrated with multi-omic data to identify endotypes. We present Merged Affinity Network Association Clustering (MANAclust), a coding-free, automated pipeline enabling integration of categorical and numeric data spanning clinical and multi-omic profiles for unsupervised clustering to identify disease subsets. Using simulations and real-world data from The Cancer Genome Atlas, we demonstrate that MANAclust’s feature selection algorithms are accurate and outperform competitors. We also apply MANAclust to a clinically and multi-omically phenotyped asthma cohort. MANAclust identifies clinically and molecularly distinct clusters, including heterogeneous groups of “healthy controls” and viral and allergy-driven subsets of asthmatic subjects. We also find that subjects with similar clinical presentations have disparate molecular profiles, highlighting the need for additional testing to uncover asthma endotypes. This work facilitates data-driven personalized medicine through integration of clinical parameters with multi-omics. MANAclust is freely available at https://bitbucket.org/scottyler892/manaclust/src/master/. |
format | Online Article Text |
id | pubmed-8195153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-81951532021-06-11 Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes Tyler, Scott R. Chun, Yoojin Ribeiro, Victoria M. Grishina, Galina Grishin, Alexander Hoffman, Gabriel E. Do, Anh N. Bunyavanich, Supinda Cell Rep Article Although clinical and laboratory data have long been used to guide medical practice, this information is rarely integrated with multi-omic data to identify endotypes. We present Merged Affinity Network Association Clustering (MANAclust), a coding-free, automated pipeline enabling integration of categorical and numeric data spanning clinical and multi-omic profiles for unsupervised clustering to identify disease subsets. Using simulations and real-world data from The Cancer Genome Atlas, we demonstrate that MANAclust’s feature selection algorithms are accurate and outperform competitors. We also apply MANAclust to a clinically and multi-omically phenotyped asthma cohort. MANAclust identifies clinically and molecularly distinct clusters, including heterogeneous groups of “healthy controls” and viral and allergy-driven subsets of asthmatic subjects. We also find that subjects with similar clinical presentations have disparate molecular profiles, highlighting the need for additional testing to uncover asthma endotypes. This work facilitates data-driven personalized medicine through integration of clinical parameters with multi-omics. MANAclust is freely available at https://bitbucket.org/scottyler892/manaclust/src/master/. 2021-04-13 /pmc/articles/PMC8195153/ /pubmed/33852839 http://dx.doi.org/10.1016/j.celrep.2021.108975 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Tyler, Scott R. Chun, Yoojin Ribeiro, Victoria M. Grishina, Galina Grishin, Alexander Hoffman, Gabriel E. Do, Anh N. Bunyavanich, Supinda Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes |
title | Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes |
title_full | Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes |
title_fullStr | Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes |
title_full_unstemmed | Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes |
title_short | Merged Affinity Network Association Clustering: Joint multi-omic/clinical clustering to identify disease endotypes |
title_sort | merged affinity network association clustering: joint multi-omic/clinical clustering to identify disease endotypes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195153/ https://www.ncbi.nlm.nih.gov/pubmed/33852839 http://dx.doi.org/10.1016/j.celrep.2021.108975 |
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