4,699 research outputs found
Fast joint detection-estimation of evoked brain activity in event-related fMRI using a variational approach
In standard clinical within-subject analyses of event-related fMRI data, two
steps are usually performed separately: detection of brain activity and
estimation of the hemodynamic response. Because these two steps are inherently
linked, we adopt the so-called region-based Joint Detection-Estimation (JDE)
framework that addresses this joint issue using a multivariate inference for
detection and estimation. JDE is built by making use of a regional bilinear
generative model of the BOLD response and constraining the parameter estimation
by physiological priors using temporal and spatial information in a Markovian
modeling. In contrast to previous works that use Markov Chain Monte Carlo
(MCMC) techniques to approximate the resulting intractable posterior
distribution, we recast the JDE into a missing data framework and derive a
Variational Expectation-Maximization (VEM) algorithm for its inference. A
variational approximation is used to approximate the Markovian model in the
unsupervised spatially adaptive JDE inference, which allows fine automatic
tuning of spatial regularisation parameters. It follows a new algorithm that
exhibits interesting properties compared to the previously used MCMC-based
approach. Experiments on artificial and real data show that VEM-JDE is robust
to model mis-specification and provides computational gain while maintaining
good performance in terms of activation detection and hemodynamic shape
recovery
Selection of sequence motifs and generative Hopfield-Potts models for protein familiesilies
Statistical models for families of evolutionary related proteins have
recently gained interest: in particular pairwise Potts models, as those
inferred by the Direct-Coupling Analysis, have been able to extract information
about the three-dimensional structure of folded proteins, and about the effect
of amino-acid substitutions in proteins. These models are typically requested
to reproduce the one- and two-point statistics of the amino-acid usage in a
protein family, {\em i.e.}~to capture the so-called residue conservation and
covariation statistics of proteins of common evolutionary origin. Pairwise
Potts models are the maximum-entropy models achieving this. While being
successful, these models depend on huge numbers of {\em ad hoc} introduced
parameters, which have to be estimated from finite amount of data and whose
biophysical interpretation remains unclear. Here we propose an approach to
parameter reduction, which is based on selecting collective sequence motifs. It
naturally leads to the formulation of statistical sequence models in terms of
Hopfield-Potts models. These models can be accurately inferred using a mapping
to restricted Boltzmann machines and persistent contrastive divergence. We show
that, when applied to protein data, even 20-40 patterns are sufficient to
obtain statistically close-to-generative models. The Hopfield patterns form
interpretable sequence motifs and may be used to clusterize amino-acid
sequences into functional sub-families. However, the distributed collective
nature of these motifs intrinsically limits the ability of Hopfield-Potts
models in predicting contact maps, showing the necessity of developing models
going beyond the Hopfield-Potts models discussed here.Comment: 26 pages, 16 figures, to app. in PR
Observational-Interventional Priors for Dose-Response Learning
Controlled interventions provide the most direct source of information for
learning causal effects. In particular, a dose-response curve can be learned by
varying the treatment level and observing the corresponding outcomes. However,
interventions can be expensive and time-consuming. Observational data, where
the treatment is not controlled by a known mechanism, is sometimes available.
Under some strong assumptions, observational data allows for the estimation of
dose-response curves. Estimating such curves nonparametrically is hard: sample
sizes for controlled interventions may be small, while in the observational
case a large number of measured confounders may need to be marginalized. In
this paper, we introduce a hierarchical Gaussian process prior that constructs
a distribution over the dose-response curve by learning from observational
data, and reshapes the distribution with a nonparametric affine transform
learned from controlled interventions. This function composition from different
sources is shown to speed-up learning, which we demonstrate with a thorough
sensitivity analysis and an application to modeling the effect of therapy on
cognitive skills of premature infants
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