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      Derivatives and Inverse of Cascaded Linear+Nonlinear Neural Models

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          Abstract

          In vision science, cascades of Linear+Nonlinear transforms explain a number of perceptual experiences [Carandini&Heeger Nat.Rev.Neur.12]. However, the conventional literature is usually too focused on only describing the forward input-output transform. Instead, in this work we present the mathematical details of such cascades beyond the forward transform, namely the derivatives and the inverse. These analytic results (usually omitted) are important for three reasons: (a) they are strictly necessary in new experimental methods based on the synthesis of visual stimuli with interesting geometrical properties, (b) they are convenient to analyze classical experiments for model fitting, and (c) they represent a promising way to include model information in blind visual decoding methods. Besides, statistical properties of the model are more intuitive by using vector representations. As an example, we develop a derivable and invertible vision model consisting of a cascade of modules that account for brightness, contrast, energy masking, and wavelet masking. To stress the generality of this modular setting we show examples where some of the canonical Divisive Normalizations [Carandini&Heeger Nat.Rev.Neur.12] are substituted by equivalent modules such as the Wilson-Cowan interaction [Wilson&Cowan J.Biophys.72] (at the V1 cortex) or a tone-mapping [Cyriac et al. SPIE 15] (at the retina). We illustrate the presented theory with three applications. First, we show how the Jacobian w.r.t. the input plays a major role in setting the model by allowing the use of novel psychophysics based on the geometry of the neural representation (as in [Malo&Simoncelli SPIE 15]). Second, we show how the Jacobian w.r.t. the parameters can be used to find the model that better reproduces image distortion psychophysics. Third, we show that analytic inverse may improve regression-based brain decoding techniques.

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          Identifying natural images from human brain activity.

          A challenging goal in neuroscience is to be able to read out, or decode, mental content from brain activity. Recent functional magnetic resonance imaging (fMRI) studies have decoded orientation, position and object category from activity in visual cortex. However, these studies typically used relatively simple stimuli (for example, gratings) or images drawn from fixed categories (for example, faces, houses), and decoding was based on previous measurements of brain activity evoked by those same stimuli or categories. To overcome these limitations, here we develop a decoding method based on quantitative receptive-field models that characterize the relationship between visual stimuli and fMRI activity in early visual areas. These models describe the tuning of individual voxels for space, orientation and spatial frequency, and are estimated directly from responses evoked by natural images. We show that these receptive-field models make it possible to identify, from a large set of completely novel natural images, which specific image was seen by an observer. Identification is not a mere consequence of the retinotopic organization of visual areas; simpler receptive-field models that describe only spatial tuning yield much poorer identification performance. Our results suggest that it may soon be possible to reconstruct a picture of a person's visual experience from measurements of brain activity alone.
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            Mean squared error: Love it or leave it? A new look at Signal Fidelity Measures

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              Application of fourier analysis to the visibility of gratings

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                Author and article information

                Journal
                01 November 2017
                Article
                1711.00526
                2466f703-ce41-49f5-b43e-21969b957474

                http://arxiv.org/licenses/nonexclusive-distrib/1.0/

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                Custom metadata
                Reproducible results: associated Matlab toolbox available at http://isp.uv.es/docs/MultiLayer_L_NL.zip
                q-bio.NC

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