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Caroline Haimerl

dblp:255/7004 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2019
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Computational science and engineering · 50% Bioinformatics and computational biology · 50%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › computational neuroscience › neural coding
neural population coding
0.412019
Flexible information routing in neural populations through stochastic comodulation · NeurIPS 2019
Computational science and engineering
theoretical neuroscience
0.412019
Flexible information routing in neural populations through stochastic comodulation · NeurIPS 2019

Methods — techniques the papers use, named apart from their topics

supervised learning · 0.4linear decoder · 0.4
YearPublicationVenuePosition
2019 Flexible information routing in neural populations through stochastic comodulation
abstract
Humans and animals are capable of flexibly switching between a multitude of tasks, each requiring rapid, sensory-informed decision making. Incoming stimuli are processed by a hierarchy of neural circuits consisting of millions of neurons with diverse feature selectivity. At any given moment, only a small subset of these carry task-relevant information. In principle, downstream processing stages could identify the relevant neurons through supervised learning, but this would require many example trials. Such extensive learning periods are inconsistent with the observed flexibility of humans or animals, who can adjust to changes in task parameters or structure almost immediately. Here, we propose a novel solution based on functionally-targeted stochastic modulation. It has been observed that trial-to-trial neural activity is modulated by a shared, low-dimensional, stochastic signal that introduces task-irrelevant noise. Counter-intuitively this noise is preferentially targeted towards task-informative neurons, corrupting the encoded signal. However, we hypothesize that this modulation offers a solution to the identification problem, labeling task-informative neurons so as to facilitate decoding. We simulate an encoding population of spiking neurons whose rates are modulated by a shared stochastic signal, and show that a linear decoder with readout weights approximating neuron-specific modulation strength can achieve near-optimal accuracy. Such a decoder allows fast and flexible task-dependent information routing without relying on hardwired knowledge of the task-informative neurons (as in maximum likelihood) or unrealistically many supervised training trials (as in regression).
Caroline Haimerl, Cristina Savin, Eero P. Simoncelli
NeurIPS1