TY - JOUR
T1 - Unsupervised Discovery of Demixed, Low-Dimensional Neural Dynamics across Multiple Timescales through Tensor Component Analysis
AU - Williams, Alex H.
AU - Kim, Tony Hyun
AU - Wang, Forea
AU - Vyas, Saurabh
AU - Ryu, Stephen I.
AU - Shenoy, Krishna V.
AU - Schnitzer, Mark
AU - Kolda, Tamara G.
AU - Ganguli, Surya
N1 - Funding Information:
The authors thank Subhaneil Lahiri (Stanford University), Jeff Seely (Cognescent Corporation), and Casey Battaglino (Georgia Tech) for discussions pertaining to this work. A.H.W. was supported by the Department of Energy Computational Science Graduate Fellowship program. T.H.K. was supported by a Stanford Graduate Fellowship in Science & Engineering. F.W. was supported by a National Science Foundation Graduate Research Fellowship. S.V. was supported by NIH F31 Ruth L. Kirschstein National Research Service Award 1F31NS103409-01, an NSF Graduate Research Fellowship, and a Ric Weiland Stanford Graduate Fellowship. K.V.S. was supported by the following awards: NIH National Institute of Neurological Disorders and Stroke (NINDS) Transformative Research Award R01NS076460, NIH National Institute of Mental Health Grant (NIMH) Transformative Research Award R01MH09964703, NIH Director's Pioneer Award 8DP1HD075623, Defense Advanced Research Projects Agency (DARPA) Biological Technology Office (BTO) ?REPAIR? award N66001-10-C-2010, DARPA BTO ?NeuroFAST? award W911NF-14-2-0013, the Simons Foundation Collaboration on the Global Brain awards 325380 and 543045, and the Howard Hughes Medical Institute. M.S. was supported by the NIH (#1R21NS104833-01), the National Science Foundation (#1707261), and the Howard Hughes Medical Institute. Work by T.G.K. was supported by the U.S. Department of Energy, Office of Science, Office of Advanced Scientific Computing Research, Applied Mathematics program in a grant to Sandia National Laboratories, a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia, LLC., a wholly owned subsidiary of Honeywell International, Inc., for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-NA-0003525. S.G. was supported by the Burroughs Wellcome Foundation, the McKnight Foundation, the James S. McDonnell Foundation, the Simons Foundation, and the Office of Naval Research. The authors thank W.L. Gore, Inc. for donating Preclude artificial dura used as part of the chronic electrode array implantation procedure used in the primate BMI task.
Funding Information:
The authors thank Subhaneil Lahiri (Stanford University), Jeff Seely (Cognescent Corporation), and Casey Battaglino (Georgia Tech) for discussions pertaining to this work. A.H.W. was supported by the Department of Energy Computational Science Graduate Fellowship program. T.H.K. was supported by a Stanford Graduate Fellowship in Science & Engineering. F.W. was supported by a National Science Foundation Graduate Research Fellowship. S.V. was supported by NIH F31 Ruth L. Kirschstein National Research Service Award 1F31NS103409-01, an NSF Graduate Research Fellowship, and a Ric Weiland Stanford Graduate Fellowship. K.V.S. was supported by the following awards: NIH National Institute of Neurological Disorders and Stroke (NINDS) Transformative Research Award R01NS076460, NIH National Institute of Mental Health Grant (NIMH) Transformative Research Award R01MH09964703, NIH Director's Pioneer Award 8DP1HD075623, Defense Advanced Research Projects Agency (DARPA) Biological Technology Office (BTO) “REPAIR” award N66001-10-C-2010, DARPA BTO “NeuroFAST” award W911NF-14-2-0013, the Simons Foundation Collaboration on the Global Brain awards 325380 and 543045, and the Howard Hughes Medical Institute. M.S. was supported by the NIH (#1R21NS104833-01), the National Science Foundation (#1707261), and the Howard Hughes Medical Institute. Work by T.G.K. was supported by the U.S. Department of Energy, Office of Science, Office of Advanced Scientific Computing Research, Applied Mathematics program in a grant to Sandia National Laboratories, a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia, LLC., a wholly owned subsidiary of Honeywell International, Inc., for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-NA-0003525. S.G. was supported by the Burroughs Wellcome Foundation, the McKnight Foundation, the James S. McDonnell Foundation, the Simons Foundation, and the Office of Naval Research. The authors thank W.L. Gore, Inc. for donating Preclude artificial dura used as part of the chronic electrode array implantation procedure used in the primate BMI task.
Funding Information:
The authors thank Subhaneil Lahiri (Stanford University), Jeff Seely (Cognescent Corporation), and Casey Battaglino (Georgia Tech) for discussions pertaining to this work. A.H.W. was supported by the Department of Energy Computational Science Graduate Fellowship program . T.H.K. was supported by a Stanford Graduate Fellowship in Science & Engineering . F.W. was supported by a National Science Foundation Graduate Research Fellowship . S.V. was supported by NIH F31 Ruth L. Kirschstein National Research Service Award 1F31NS103409-01 , an NSF Graduate Research Fellowship, and a Ric Weiland Stanford Graduate Fellowship . K.V.S. was supported by the following awards: NIH National Institute of Neurological Disorders and Stroke (NINDS) Transformative Research Award R01NS076460 , NIH National Institute of Mental Health Grant (NIMH) Transformative Research Award R01MH09964703 , NIH Director’s Pioneer Award 8DP1HD075623 , Defense Advanced Research Projects Agency (DARPA) Biological Technology Office (BTO) “REPAIR” award N66001-10-C-2010 , DARPA BTO “NeuroFAST” award W911NF-14-2-0013 , the Simons Foundation Collaboration on the Global Brain awards 325380 and 543045 , and the Howard Hughes Medical Institute . M.S. was supported by the NIH (# 1R21NS104833-01 ), the National Science Foundation (# 1707261 ), and the Howard Hughes Medical Institute . Work by T.G.K. was supported by the U.S. Department of Energy , Office of Science, Office of Advanced Scientific Computing Research, Applied Mathematics program in a grant to Sandia National Laboratories, a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia, LLC., a wholly owned subsidiary of Honeywell International, Inc., for the U.S. Department of Energy’s National Nuclear Security Administration under contract DE-NA-0003525 . S.G. was supported by the Burroughs Wellcome Foundation , the McKnight Foundation , the James S. McDonnell Foundation , the Simons Foundation , and the Office of Naval Research . The authors thank W.L. Gore, Inc. for donating Preclude artificial dura used as part of the chronic electrode array implantation procedure used in the primate BMI task.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/6/27
Y1 - 2018/6/27
N2 - Perceptions, thoughts, and actions unfold over millisecond timescales, while learned behaviors can require many days to mature. While recent experimental advances enable large-scale and long-term neural recordings with high temporal fidelity, it remains a formidable challenge to extract unbiased and interpretable descriptions of how rapid single-trial circuit dynamics change slowly over many trials to mediate learning. We demonstrate a simple tensor component analysis (TCA) can meet this challenge by extracting three interconnected, low-dimensional descriptions of neural data: neuron factors, reflecting cell assemblies; temporal factors, reflecting rapid circuit dynamics mediating perceptions, thoughts, and actions within each trial; and trial factors, describing both long-term learning and trial-to-trial changes in cognitive state. We demonstrate the broad applicability of TCA by revealing insights into diverse datasets derived from artificial neural networks, large-scale calcium imaging of rodent prefrontal cortex during maze navigation, and multielectrode recordings of macaque motor cortex during brain machine interface learning. Williams et al. describe an unsupervised method to uncover simple structure in large-scale recordings by extracting distinct cell assemblies with rapid within-trial dynamics, reflecting interpretable aspects of perceptions, actions, and thoughts, and slower across-trial dynamics reflecting learning and internal state changes.
AB - Perceptions, thoughts, and actions unfold over millisecond timescales, while learned behaviors can require many days to mature. While recent experimental advances enable large-scale and long-term neural recordings with high temporal fidelity, it remains a formidable challenge to extract unbiased and interpretable descriptions of how rapid single-trial circuit dynamics change slowly over many trials to mediate learning. We demonstrate a simple tensor component analysis (TCA) can meet this challenge by extracting three interconnected, low-dimensional descriptions of neural data: neuron factors, reflecting cell assemblies; temporal factors, reflecting rapid circuit dynamics mediating perceptions, thoughts, and actions within each trial; and trial factors, describing both long-term learning and trial-to-trial changes in cognitive state. We demonstrate the broad applicability of TCA by revealing insights into diverse datasets derived from artificial neural networks, large-scale calcium imaging of rodent prefrontal cortex during maze navigation, and multielectrode recordings of macaque motor cortex during brain machine interface learning. Williams et al. describe an unsupervised method to uncover simple structure in large-scale recordings by extracting distinct cell assemblies with rapid within-trial dynamics, reflecting interpretable aspects of perceptions, actions, and thoughts, and slower across-trial dynamics reflecting learning and internal state changes.
KW - brain machine interfaces
KW - dimensionality reduction
KW - gain modulation
KW - large-scale recordings
KW - learning
KW - motor control
KW - navigation
KW - neural data analysis
KW - recurrent neural networks
KW - single-trial analysis
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U2 - 10.1016/j.neuron.2018.05.015
DO - 10.1016/j.neuron.2018.05.015
M3 - Article
C2 - 29887338
AN - SCOPUS:85047777491
VL - 98
SP - 1099-1115.e8
JO - Neuron
JF - Neuron
SN - 0896-6273
IS - 6
ER -