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Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures
Unravelling protein distributions within individual cells is vital to understanding their function and state and indispensable to developing new treatments. Here we present the Hybrid subCellular Protein Localiser (HCPL), which learns from weakly labelled data to robustly localise single-cell subcel...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163260/ https://www.ncbi.nlm.nih.gov/pubmed/37147530 http://dx.doi.org/10.1038/s42003-023-04840-z |
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author | Husain, Syed Sameed Ong, Eng-Jon Minskiy, Dmitry Bober-Irizar, Mikel Irizar, Amaia Bober, Miroslaw |
author_facet | Husain, Syed Sameed Ong, Eng-Jon Minskiy, Dmitry Bober-Irizar, Mikel Irizar, Amaia Bober, Miroslaw |
author_sort | Husain, Syed Sameed |
collection | PubMed |
description | Unravelling protein distributions within individual cells is vital to understanding their function and state and indispensable to developing new treatments. Here we present the Hybrid subCellular Protein Localiser (HCPL), which learns from weakly labelled data to robustly localise single-cell subcellular protein patterns. It comprises innovative DNN architectures exploiting wavelet filters and learnt parametric activations that successfully tackle drastic cell variability. HCPL features correlation-based ensembling of novel architectures that boosts performance and aids generalisation. Large-scale data annotation is made feasible by our AI-trains-AI approach, which determines the visual integrity of cells and emphasises reliable labels for efficient training. In the Human Protein Atlas context, we demonstrate that HCPL is best performing in the single-cell classification of protein localisation patterns. To better understand the inner workings of HCPL and assess its biological relevance, we analyse the contributions of each system component and dissect the emergent features from which the localisation predictions are derived. |
format | Online Article Text |
id | pubmed-10163260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101632602023-05-07 Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures Husain, Syed Sameed Ong, Eng-Jon Minskiy, Dmitry Bober-Irizar, Mikel Irizar, Amaia Bober, Miroslaw Commun Biol Article Unravelling protein distributions within individual cells is vital to understanding their function and state and indispensable to developing new treatments. Here we present the Hybrid subCellular Protein Localiser (HCPL), which learns from weakly labelled data to robustly localise single-cell subcellular protein patterns. It comprises innovative DNN architectures exploiting wavelet filters and learnt parametric activations that successfully tackle drastic cell variability. HCPL features correlation-based ensembling of novel architectures that boosts performance and aids generalisation. Large-scale data annotation is made feasible by our AI-trains-AI approach, which determines the visual integrity of cells and emphasises reliable labels for efficient training. In the Human Protein Atlas context, we demonstrate that HCPL is best performing in the single-cell classification of protein localisation patterns. To better understand the inner workings of HCPL and assess its biological relevance, we analyse the contributions of each system component and dissect the emergent features from which the localisation predictions are derived. Nature Publishing Group UK 2023-05-05 /pmc/articles/PMC10163260/ /pubmed/37147530 http://dx.doi.org/10.1038/s42003-023-04840-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Husain, Syed Sameed Ong, Eng-Jon Minskiy, Dmitry Bober-Irizar, Mikel Irizar, Amaia Bober, Miroslaw Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures |
title | Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures |
title_full | Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures |
title_fullStr | Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures |
title_full_unstemmed | Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures |
title_short | Single-cell subcellular protein localisation using novel ensembles of diverse deep architectures |
title_sort | single-cell subcellular protein localisation using novel ensembles of diverse deep architectures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163260/ https://www.ncbi.nlm.nih.gov/pubmed/37147530 http://dx.doi.org/10.1038/s42003-023-04840-z |
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