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DeepMF: deciphering the latent patterns in omics profiles with a deep learning method
BACKGROUND: With recent advances in high-throughput technologies, matrix factorization techniques are increasingly being utilized for mapping quantitative omics profiling matrix data into low-dimensional embedding space, in the hope of uncovering insights in the underlying biological processes. Neve...
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/PMC6933662/ https://www.ncbi.nlm.nih.gov/pubmed/31881818 http://dx.doi.org/10.1186/s12859-019-3291-6 |
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author | Chen, Lingxi Xu, Jiao Li, Shuai Cheng |
author_facet | Chen, Lingxi Xu, Jiao Li, Shuai Cheng |
author_sort | Chen, Lingxi |
collection | PubMed |
description | BACKGROUND: With recent advances in high-throughput technologies, matrix factorization techniques are increasingly being utilized for mapping quantitative omics profiling matrix data into low-dimensional embedding space, in the hope of uncovering insights in the underlying biological processes. Nevertheless, current matrix factorization tools fall short in handling noisy data and missing entries, both deficiencies that are often found in real-life data. RESULTS: Here, we propose DeepMF, a deep neural network-based factorization model. DeepMF disentangles the association between molecular feature-associated and sample-associated latent matrices, and is tolerant to noisy and missing values. It exhibited feasible cancer subtype discovery efficacy on mRNA, miRNA, and protein profiles of medulloblastoma cancer, leukemia cancer, breast cancer, and small-blue-round-cell cancer, achieving the highest clustering accuracy of 76%, 100%, 92%, and 100% respectively. When analyzing data sets with 70% missing entries, DeepMF gave the best recovery capacity with silhouette values of 0.47, 0.6, 0.28, and 0.44, outperforming other state-of-the-art MF tools on the cancer data sets Medulloblastoma, Leukemia, TCGA BRCA, and SRBCT. Its embedding strength as measured by clustering accuracy is 88%, 100%, 84%, and 96% on these data sets, which improves on the current best methods 76%, 100%, 78%, and 87%. CONCLUSION: DeepMF demonstrated robust denoising, imputation, and embedding ability. It offers insights to uncover the underlying biological processes such as cancer subtype discovery. Our implementation of DeepMF can be found at https://github.com/paprikachan/DeepMF. |
format | Online Article Text |
id | pubmed-6933662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69336622019-12-30 DeepMF: deciphering the latent patterns in omics profiles with a deep learning method Chen, Lingxi Xu, Jiao Li, Shuai Cheng BMC Bioinformatics Methodology BACKGROUND: With recent advances in high-throughput technologies, matrix factorization techniques are increasingly being utilized for mapping quantitative omics profiling matrix data into low-dimensional embedding space, in the hope of uncovering insights in the underlying biological processes. Nevertheless, current matrix factorization tools fall short in handling noisy data and missing entries, both deficiencies that are often found in real-life data. RESULTS: Here, we propose DeepMF, a deep neural network-based factorization model. DeepMF disentangles the association between molecular feature-associated and sample-associated latent matrices, and is tolerant to noisy and missing values. It exhibited feasible cancer subtype discovery efficacy on mRNA, miRNA, and protein profiles of medulloblastoma cancer, leukemia cancer, breast cancer, and small-blue-round-cell cancer, achieving the highest clustering accuracy of 76%, 100%, 92%, and 100% respectively. When analyzing data sets with 70% missing entries, DeepMF gave the best recovery capacity with silhouette values of 0.47, 0.6, 0.28, and 0.44, outperforming other state-of-the-art MF tools on the cancer data sets Medulloblastoma, Leukemia, TCGA BRCA, and SRBCT. Its embedding strength as measured by clustering accuracy is 88%, 100%, 84%, and 96% on these data sets, which improves on the current best methods 76%, 100%, 78%, and 87%. CONCLUSION: DeepMF demonstrated robust denoising, imputation, and embedding ability. It offers insights to uncover the underlying biological processes such as cancer subtype discovery. Our implementation of DeepMF can be found at https://github.com/paprikachan/DeepMF. BioMed Central 2019-12-27 /pmc/articles/PMC6933662/ /pubmed/31881818 http://dx.doi.org/10.1186/s12859-019-3291-6 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative 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 Chen, Lingxi Xu, Jiao Li, Shuai Cheng DeepMF: deciphering the latent patterns in omics profiles with a deep learning method |
title | DeepMF: deciphering the latent patterns in omics profiles with a deep learning method |
title_full | DeepMF: deciphering the latent patterns in omics profiles with a deep learning method |
title_fullStr | DeepMF: deciphering the latent patterns in omics profiles with a deep learning method |
title_full_unstemmed | DeepMF: deciphering the latent patterns in omics profiles with a deep learning method |
title_short | DeepMF: deciphering the latent patterns in omics profiles with a deep learning method |
title_sort | deepmf: deciphering the latent patterns in omics profiles with a deep learning method |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933662/ https://www.ncbi.nlm.nih.gov/pubmed/31881818 http://dx.doi.org/10.1186/s12859-019-3291-6 |
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