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@INPROCEEDINGS{DeBonis:873849,
author = {De Bonis, Giulia and Pastorelli, Elena and Capone,
Cristiano and Gutzen, Robin and Camassa, Alessandra and
Berengué, Arnau Manasanch and Resta, Francesco and Mascaro,
Anna Letizia Allegra and Pazienti, Antonio and Pigorini,
Andrea and Nieus, Thierry and Arena, Alessandro and Storm,
Johan Frederik and Massimini, Marcello and Pavone, Francesco
Saverio and Sanchez-Vives, Maria V. and Mattia, Maurizio and
Davison, Andrew and Denker, Michael and Paolucci, Pier
Stanislao},
title = {{M}ulti-scale, multi-species, multi-methodology
experiments, analysis tools and simulation models of {B}rain
{S}tates and {C}omplexity in {SP}3-{U}se{C}ase002},
reportid = {FZJ-2020-01051},
year = {2020},
abstract = {The general goal of SP3-UseCase002 is to offer to external
users, through EBRAINS Knowledge Graph, an integrated
environment, dedicated to the topic of cortical slow wave
activity (SWA) [1,2] in spontaneous and perturbed mode, and
to sleep/awake transitions, measures of complexity (like
PCI, perturbational complexity index) and the cognitive
effects of sleep in thalamo-cortical systems. The offering
includes multi-scale multi-species experimental data,
simulation models, simulation results, and analysis tools.
The analysis tools are designed to be applicable to both
experimental data and simulation results since, for a fair
comparison and accurate validation of the models, the
outcome of data-driven biologically-plausible simulations
[3] should be subjected to the same analysis tools used for
the data. We note that the variety of the experimental
techniques for data acquisition and the diversity of
subjects and species involved (due to large biological
variability, but also to brain states,
physiological/pathological conditions, drug doses and data
taking setups) make challenging the building of reliable and
generalizable data analysis tools aimed at identifying
common observables when comparing the outcome of different
experiments acquired with different experimental modalities,
and at obtaining reproducible results.SP3-UseCase002
integrates the results of WP3.2 (aka WaveScalES, focusing on
sleep, anaesthesia and transition to wakefulness, KR3.2) and
WP3.4 (aka ConsciousBrain, focusing on neural correlates and
measure of consciousness in physiological and pathological
brains, KR3.4).The analysis pipeline developed by WaveScalES
[4,5], when applied to experimental data, enables the
extraction of key spatio-temporal characteristics from slow
waves acquired with multiple experimental methodologies
(using micro-ECoG arrays and wide-field Calcium imaging
techniques, to be extended to hd-EEG and stereo-EEG), at
local and multi-areal spatial resolution. The platform also
includes simulation models of SWA and AW-like cortical
activity at biologically-plausible neural and synaptic
densities [6] and simulation models demonstrating the
effects of interactions among sleep and memories and the
changes in cognitive performances of thalamo-cortical models
passing through wakefulness-sleep-wakefulness cycles [7].
When applied to simulation results, similar features should
be extracted, to enable a quantitative comparison between
simulation and experimental data, fostering a better
calibration of simulations.Concerning the ConsciousBrain
research, the measure is based on a perturbational approach
(i.e. perturbing the brain with an exogenous input and
gauging the derived spatiotemporal dynamics). The proposed
analysis pipeline calculates several complexity indices on
multi-scale experimental data that includes TMS-EEG data in
healthy humans and patients with disorder of consciousness,
intracerebral recordings in epileptic patients undergoing
presurgical evaluation as well as spikes and LFP signals in
rats/mice. The Perturbational Complexity Index based on
Lempel and Ziv algorithm (PCIlz)[8] correlates with the
level of consciousness and has been validated using TMS-EEG
data collected from a large cohort of healthy subjects and
patients affected by disorder of consciousness [9]; the
Perturbational Complexity Index based on State Transitions
(PCIst)[10] is faster than PCIlz, it does not depend on
source modelling algorithms and can be applied on data
different from scalp EEG. In addition, a revisited version
of PCIlz, calibrated on TMS/EEG and extracellular signals
from cerebellar brain slices, will also be included.Here, we
present the status of the implementation of the Use Case,
with some preliminary results and conclusions.References 1.
Steriade (1993), Journal of Neuroscience. 2. Sanchez-Vives,
M.V. et al (2017), Neuron. 3. Capone C et al., Cerebral
cortex (2019): 29, 1. 4. De Bonis, G. et al. (2019) Front.
Syst. Neurosci, 13, 70. 5. Celotto M, et al (2018),
arXiv:1811.11687 6. Pastorelli, E. et al. (2019) Front.
Syst. Neurosci 13, 33. 7. Capone C., et al (2019), Sci. Rep.
9, 8990 8. Casali et al Science Tr. Med, 2013 9. Casarotto
et al Ann. of Neurol, 2016 10. Comolatti et al. Brain Stim,
2019},
month = {Feb},
date = {2020-02-03},
organization = {Human Brain Project Summit, Athens
(Greece), 3 Feb 2020 - 6 Feb 2020},
subtyp = {Invited},
cin = {INM-6 / INM-10 / IAS-6},
cid = {I:(DE-Juel1)INM-6-20090406 / I:(DE-Juel1)INM-10-20170113 /
I:(DE-Juel1)IAS-6-20130828},
pnm = {571 - Connectivity and Activity (POF3-571) / 574 - Theory,
modelling and simulation (POF3-574) / HBP SGA2 - Human Brain
Project Specific Grant Agreement 2 (785907)},
pid = {G:(DE-HGF)POF3-571 / G:(DE-HGF)POF3-574 /
G:(EU-Grant)785907},
typ = {PUB:(DE-HGF)24},
url = {https://juser.fz-juelich.de/record/873849},
}