Evidence map›Paper›PMID 37954574›Full record

ArticleNAR genomics and bioinformatics2023

SnapKin: a snapshot deep learning ensemble for kinase-substrate prediction from phosphoproteomics data.

Di Xiao, Michael Lin, Chunlei Liu, Thomas A Geddes, James G Burchfield, Benjamin L Parker, Sean J Humphrey, Pengyi Yang

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Di XiaoComputational Systems Biology Group, Children's Medical Research Institute, The University of Sydney, Westmead, NSW 2145, Australia.
Michael LinSchool of Mathematics and Statistics, The University of Sydney, Sydney, NSW 2006, Australia.
Chunlei LiuComputational Systems Biology Group, Children's Medical Research Institute, The University of Sydney, Westmead, NSW 2145, Australia.
Thomas A GeddesComputational Systems Biology Group, Children's Medical Research Institute, The University of Sydney, Westmead, NSW 2145, Australia.
James G BurchfieldCharles Perkins Centre, The University of Sydney, Sydney, NSW 2006, Australia.
Benjamin L ParkerCentre for Muscle Research, Department of Anatomy and Physiology, School of Biomedical Sciences, Melbourne, VIC 3010, Australia.ORCID https://orcid.org/0000-0003-1818-2183
Sean J HumphreyCharles Perkins Centre, The University of Sydney, Sydney, NSW 2006, Australia.ORCID https://orcid.org/0000-0002-2666-9744
Pengyi YangComputational Systems Biology Group, Children's Medical Research Institute, The University of Sydney, Westmead, NSW 2145, Australia.ORCID https://orcid.org/0000-0003-1098-3138

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major challenge in mass spectrometry-based phosphoproteomics lies in identifying the substrates of kinases, as currently only a small fraction of substrates identified can be confidently linked with a known kinase. Machine learning techniques are promising approaches for leveraging large-scale phosphoproteomics data to computationally predict substrates of kinases. However, the small number of experimentally validated kinase substrates (true positive) and the high data noise in many phosphoproteomics datasets together limit their applicability and utility. Here, we aim to develop advanced kinase-substrate prediction methods to address these challenges. Using a collection of seven large phosphoproteomics datasets, and both traditional and deep learning models, we first demonstrate that a 'pseudo-positive' learning strategy for alleviating small sample size is effective at improving model predictive performance. We next show that a data resampling-based ensemble learning strategy is useful for improving model stability while further enhancing prediction. Lastly, we introduce an ensemble deep learning model ('SnapKin') by incorporating the above two learning strategies into a 'snapshot' ensemble learning algorithm. We propose SnapKin, an ensemble deep learning method, for predicting substrates of kinases from large-scale phosphoproteomics data. We demonstrate that SnapKin consistently outperforms existing methods in kinase-substrate prediction. SnapKin is freely available at https://github.com/PYangLab/SnapKin.

Identifiers

PMID37954574
PMCPMC10632189

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.