Cargando…

SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species

Understanding sleep and its perturbation by environment, mutation, or medication remains a central problem in biomedical research. Its examination in animal models rests on brain state analysis via classification of electroencephalographic (EEG) signatures. Traditionally, these states are classified...

Descripción completa

Detalles Bibliográficos
Autores principales: Miladinović, Đorđe, Muheim, Christine, Bauer, Stefan, Spinnler, Andrea, Noain, Daniela, Bandarabadi, Mojtaba, Gallusser, Benjamin, Krummenacher, Gabriel, Baumann, Christian, Adamantidis, Antoine, Brown, Steven A., Buhmann, Joachim M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6490936/
https://www.ncbi.nlm.nih.gov/pubmed/30998681
http://dx.doi.org/10.1371/journal.pcbi.1006968
_version_ 1783414906824949760
author Miladinović, Đorđe
Muheim, Christine
Bauer, Stefan
Spinnler, Andrea
Noain, Daniela
Bandarabadi, Mojtaba
Gallusser, Benjamin
Krummenacher, Gabriel
Baumann, Christian
Adamantidis, Antoine
Brown, Steven A.
Buhmann, Joachim M.
author_facet Miladinović, Đorđe
Muheim, Christine
Bauer, Stefan
Spinnler, Andrea
Noain, Daniela
Bandarabadi, Mojtaba
Gallusser, Benjamin
Krummenacher, Gabriel
Baumann, Christian
Adamantidis, Antoine
Brown, Steven A.
Buhmann, Joachim M.
author_sort Miladinović, Đorđe
collection PubMed
description Understanding sleep and its perturbation by environment, mutation, or medication remains a central problem in biomedical research. Its examination in animal models rests on brain state analysis via classification of electroencephalographic (EEG) signatures. Traditionally, these states are classified by trained human experts by visual inspection of raw EEG recordings, which is a laborious task prone to inter-individual variability. Recently, machine learning approaches have been developed to automate this process, but their generalization capabilities are often insufficient, especially across animals from different experimental studies. To address this challenge, we crafted a convolutional neural network-based architecture to produce domain invariant predictions, and furthermore integrated a hidden Markov model to constrain state dynamics based upon known sleep physiology. Our method, which we named SPINDLE (Sleep Phase Identification with Neural networks for Domain-invariant LEearning) was validated using data of four animal cohorts from three independent sleep labs, and achieved average agreement rates of 99%, 98%, 93%, and 97% with scorings from five human experts from different labs, essentially duplicating human capability. It generalized across different genetic mutants, surgery procedures, recording setups and even different species, far exceeding state-of-the-art solutions that we tested in parallel on this task. Moreover, we show that these scored data can be processed for downstream analyzes identical to those from human-scored data, in particular by demonstrating the ability to detect mutation-induced sleep alteration. We provide to the scientific community free usage of SPINDLE and benchmarking datasets as an online server at https://sleeplearning.ethz.ch. Our aim is to catalyze high-throughput and well-standardized experimental studies in order to improve our understanding of sleep.
format Online
Article
Text
id pubmed-6490936
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-64909362019-05-17 SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species Miladinović, Đorđe Muheim, Christine Bauer, Stefan Spinnler, Andrea Noain, Daniela Bandarabadi, Mojtaba Gallusser, Benjamin Krummenacher, Gabriel Baumann, Christian Adamantidis, Antoine Brown, Steven A. Buhmann, Joachim M. PLoS Comput Biol Research Article Understanding sleep and its perturbation by environment, mutation, or medication remains a central problem in biomedical research. Its examination in animal models rests on brain state analysis via classification of electroencephalographic (EEG) signatures. Traditionally, these states are classified by trained human experts by visual inspection of raw EEG recordings, which is a laborious task prone to inter-individual variability. Recently, machine learning approaches have been developed to automate this process, but their generalization capabilities are often insufficient, especially across animals from different experimental studies. To address this challenge, we crafted a convolutional neural network-based architecture to produce domain invariant predictions, and furthermore integrated a hidden Markov model to constrain state dynamics based upon known sleep physiology. Our method, which we named SPINDLE (Sleep Phase Identification with Neural networks for Domain-invariant LEearning) was validated using data of four animal cohorts from three independent sleep labs, and achieved average agreement rates of 99%, 98%, 93%, and 97% with scorings from five human experts from different labs, essentially duplicating human capability. It generalized across different genetic mutants, surgery procedures, recording setups and even different species, far exceeding state-of-the-art solutions that we tested in parallel on this task. Moreover, we show that these scored data can be processed for downstream analyzes identical to those from human-scored data, in particular by demonstrating the ability to detect mutation-induced sleep alteration. We provide to the scientific community free usage of SPINDLE and benchmarking datasets as an online server at https://sleeplearning.ethz.ch. Our aim is to catalyze high-throughput and well-standardized experimental studies in order to improve our understanding of sleep. Public Library of Science 2019-04-18 /pmc/articles/PMC6490936/ /pubmed/30998681 http://dx.doi.org/10.1371/journal.pcbi.1006968 Text en © 2019 Miladinović et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Miladinović, Đorđe
Muheim, Christine
Bauer, Stefan
Spinnler, Andrea
Noain, Daniela
Bandarabadi, Mojtaba
Gallusser, Benjamin
Krummenacher, Gabriel
Baumann, Christian
Adamantidis, Antoine
Brown, Steven A.
Buhmann, Joachim M.
SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species
title SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species
title_full SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species
title_fullStr SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species
title_full_unstemmed SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species
title_short SPINDLE: End-to-end learning from EEG/EMG to extrapolate animal sleep scoring across experimental settings, labs and species
title_sort spindle: end-to-end learning from eeg/emg to extrapolate animal sleep scoring across experimental settings, labs and species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6490936/
https://www.ncbi.nlm.nih.gov/pubmed/30998681
http://dx.doi.org/10.1371/journal.pcbi.1006968
work_keys_str_mv AT miladinovicđorđe spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT muheimchristine spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT bauerstefan spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT spinnlerandrea spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT noaindaniela spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT bandarabadimojtaba spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT gallusserbenjamin spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT krummenachergabriel spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT baumannchristian spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT adamantidisantoine spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT brownstevena spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies
AT buhmannjoachimm spindleendtoendlearningfromeegemgtoextrapolateanimalsleepscoringacrossexperimentalsettingslabsandspecies