36 research outputs found
A renormalization group study of a class of reaction-diffusion model, with particles input
We study a class of reaction-diffusion model extrapolating continuously
between the pure coagulation-diffusion case () and the pure
annihilation-diffusion one () with particles input
() at a rate . For dimension , the dynamics
strongly depends on the fluctuations while, for , the behaviour is
mean-field like. The models are mapped onto a field theory which properties are
studied in a renormalization group approach. Simple relations are found between
the time-dependent correlation functions of the different models of the class.
For the pure coagulation-diffusion model the time-dependent density is found to
be of the form , where
is the diffusion constant. The critical exponent and are
computed to all orders in , where is the dimension of the
system, while the scaling function is computed to second order in
. For the one-dimensional case an exact analytical solution is
provided which predictions are compared with the results of the renormalization
group approach for .Comment: Ten pages, using Latex and IOP macro. Two latex figures. Submitted to
Journal of Physics A. Also available at
http://mykonos.unige.ch/~rey/publi.htm
Equilibrium statistical mechanics on correlated random graphs
Biological and social networks have recently attracted enormous attention
between physicists. Among several, two main aspects may be stressed: A non
trivial topology of the graph describing the mutual interactions between agents
exists and/or, typically, such interactions are essentially (weighted)
imitative. Despite such aspects are widely accepted and empirically confirmed,
the schemes currently exploited in order to generate the expected topology are
based on a-priori assumptions and in most cases still implement constant
intensities for links. Here we propose a simple shift in the definition of
patterns in an Hopfield model to convert frustration into dilution: By varying
the bias of the pattern distribution, the network topology -which is generated
by the reciprocal affinities among agents - crosses various well known regimes
(fully connected, linearly diverging connectivity, extreme dilution scenario,
no network), coupled with small world properties, which, in this context, are
emergent and no longer imposed a-priori. The model is investigated at first
focusing on these topological properties of the emergent network, then its
thermodynamics is analytically solved (at a replica symmetric level) by
extending the double stochastic stability technique, and presented together
with its fluctuation theory for a picture of criticality. At least at
equilibrium, dilution simply decreases the strength of the coupling felt by the
spins, but leaves the paramagnetic/ferromagnetic flavors unchanged. The main
difference with respect to previous investigations and a naive picture is that
within our approach replicas do not appear: instead of (multi)-overlaps as
order parameters, we introduce a class of magnetizations on all the possible
sub-graphs belonging to the main one investigated: As a consequence, for these
objects a closure for a self-consistent relation is achieved.Comment: 30 pages, 4 figure
Transcriptional Dynamics Reveal Critical Roles for Non-coding RNAs in the Immediate-Early Response
<div><p>The immediate-early response mediates cell fate in response to a variety of extracellular stimuli and is dysregulated in many cancers. However, the specificity of the response across stimuli and cell types, and the roles of non-coding RNAs are not well understood. Using a large collection of densely-sampled time series expression data we have examined the induction of the immediate-early response in unparalleled detail, across cell types and stimuli. We exploit cap analysis of gene expression (CAGE) time series datasets to directly measure promoter activities over time. Using a novel analysis method for time series data we identify transcripts with expression patterns that closely resemble the dynamics of known immediate-early genes (IEGs) and this enables a comprehensive comparative study of these genes and their chromatin state. Surprisingly, these data suggest that the earliest transcriptional responses often involve promoters generating non-coding RNAs, many of which are produced in advance of canonical protein-coding IEGs. IEGs are known to be capable of induction without de novo protein synthesis. Consistent with this, we find that the response of both protein-coding and non-coding RNA IEGs can be explained by their transcriptionally poised, permissive chromatin state prior to stimulation. We also explore the function of non-coding RNAs in the attenuation of the immediate early response in a small RNA sequencing dataset matched to the CAGE data: We identify a novel set of microRNAs responsible for the attenuation of the IEG response in an estrogen receptor positive cancer cell line. Our computational statistical method is well suited to meta-analyses as there is no requirement for transcripts to pass thresholds for significant differential expression between time points, and it is agnostic to the number of time points per dataset.</p></div