507 research outputs found
Uniform random generation of large acyclic digraphs
Directed acyclic graphs are the basic representation of the structure
underlying Bayesian networks, which represent multivariate probability
distributions. In many practical applications, such as the reverse engineering
of gene regulatory networks, not only the estimation of model parameters but
the reconstruction of the structure itself is of great interest. As well as for
the assessment of different structure learning algorithms in simulation
studies, a uniform sample from the space of directed acyclic graphs is required
to evaluate the prevalence of certain structural features. Here we analyse how
to sample acyclic digraphs uniformly at random through recursive enumeration,
an approach previously thought too computationally involved. Based on
complexity considerations, we discuss in particular how the enumeration
directly provides an exact method, which avoids the convergence issues of the
alternative Markov chain methods and is actually computationally much faster.
The limiting behaviour of the distribution of acyclic digraphs then allows us
to sample arbitrarily large graphs. Building on the ideas of recursive
enumeration based sampling we also introduce a novel hybrid Markov chain with
much faster convergence than current alternatives while still being easy to
adapt to various restrictions. Finally we discuss how to include such
restrictions in the combinatorial enumeration and the new hybrid Markov chain
method for efficient uniform sampling of the corresponding graphs.Comment: 15 pages, 2 figures. To appear in Statistics and Computin
Polar Perturbations of Self-gravitating Supermassive Global Monopoles
Spontaneous global symmetry breaking of O(3) scalar field gives rise to
point-like topological defects, global monopoles. By taking into account
self-gravity,the qualitative feature of the global monopole solutions depends
on the vacuum expectation value v of the scalar field. When v < sqrt{1 / 8 pi},
there are global monopole solutions which have a deficit solid angle defined at
infinity. When sqrt{1 / 8 pi} <= v < sqrt{3 / 8 pi}, there are global monopole
solutions with the cosmological horizon, which we call the supermassive global
monopole. When v >= sqrt{3 / 8 pi}, there is no nontrivial solution. It was
shown that all of these solutions are stable against the spherical
perturbations. In addition to the global monopole solutions, the de Sitter
solutions exist for any value of v. They are stable against the spherical
perturbations when v sqrt{3 / 8 pi}.
We study polar perturbations of these solutions and find that all
self-gravitating global monopoles are stable even against polar perturbations,
independently of the existence of the cosmological horizon, while the de Sitter
solutions are always unstable.Comment: 10 pages, 6 figures, corrected some type mistakes (already corrected
in PRD version
Orthogonality conditions and asymptotic stability in the Stefan problem with surface tension
We prove nonlinear asymptotic stability of steady spheres in the two-phase
Stefan problem with surface tension. Our method relies on the introduction of
appropriate orthogonality conditions in conjunction with a high-order energy
method.Comment: 25 pages, important references added, two remarks added, typos
correcte
Jacobi-like bar mode instability of relativistic rotating bodies
We perform some numerical study of the secular triaxial instability of
rigidly rotating homogeneous fluid bodies in general relativity. In the
Newtonian limit, this instability arises at the bifurcation point between the
Maclaurin and Jacobi sequences. It can be driven in astrophysical systems by
viscous dissipation. We locate the onset of instability along several constant
baryon mass sequences of uniformly rotating axisymmetric bodies for compaction
parameter . We find that general relativity weakens the Jacobi
like bar mode instability, but the stabilizing effect is not very strong.
According to our analysis the critical value of the ratio of the kinetic energy
to the absolute value of the gravitational potential energy for compaction parameter as high as 0.275 is only 30% higher than the
Newtonian value. The critical value of the eccentricity depends very weakly on
the degree of relativity and for is only 2% larger than the
Newtonian value at the onset for the secular bar mode instability. We compare
our numerical results with recent analytical investigations based on the
post-Newtonian expansion.Comment: 15 pages, 8 figures, submitted to Phys. Rev.
An Immune Gene Expression Signature Associated With Development of Human Hepatocellular Carcinoma Identifies Mice That Respond to Chemopreventive Agents
Program (HEPCAR, reference no. 667273-2); US Department of Defense(CA150272P3); an Accelerator Award (CRUCK, AECC, AIRC) (HUNTER,reference no. C9380/A26813), NCI Cancer Center Support Grant, National Cancer Institute; Tisch Cancer Institute (P30-CA196521); Samuel Waxman Cancer Research Foundation; Spanish National Health Institute (SAF2016-76390); and the Generalitat de Catalunya/AGAUR (SGR-1358). Agrin Moeini is supported by Spanish National Health Institute. Sara Torrecilla and Judit Peix are funded by Centro de Investigación Biomedica en Red de Enfermedades Hepáticas y Digestivas (Ciberehd-ISCIII). Carla Montironi is a recipient of Josep Font grant. Carmen Andreu-Oller is supported by "la Caixa" INPhINIT Fellowship Grant (LCF/BQ/IN17/11620024). Roser Pinyol is supported by HEPCAR and AECC. Daniela Sia is supported by the Gilead Sciences Research Scholar Program in Liver Disease. Scott L. Friedman is supported by the National Institutes of Health Research project grant (R01,DK5662) and US Department of Defense (CA150272P3). Mathias Heikenwälder was supported by an ERC Consolidator grant (HepatoMetaboPath), the SFBTR 209, 1335 and SFBTR179.Background & Aims: Cirrhosis and chronic inflammation precede development of hepatocellular carcinoma (HCC) in approximately 80% of cases. We investigated immune-related gene expression patterns in liver tissues surrounding early-stage HCCs and chemopreventive agents that might alter these patterns to prevent liver tumorigenesis. Methods: We analyzed gene expression profiles of nontumor liver tissues from 392 patients with early-stage HCC (training set, N = 167 and validation set, N = 225) and liver tissue from patients with cirrhosis without HCC (N = 216, controls) to identify changes in expression of genes that regulate the immune response that could contribute to hepatocarcinogenesis. We defined 172 genes as markers for this deregulated immune response, which we called the immune-mediated cancer field (ICF). We analyzed the expression data of liver tissues from 216 patients with cirrhosis without HCC and investigated the association between this gene expression signature and development of HCC and outcomes of patients (median follow-up, 10 years). Human liver tissues were also analyzed by histology. C57BL/6J mice were given a single injection of diethylnitrosamine (DEN) followed by weekly doses of carbon tetrachloride to induce liver fibrosis and tumorigenesis. Mice were then orally given the multiple tyrosine inhibitor nintedanib or vehicle (controls); liver tissues were collected and histology, transcriptome, and protein analyses were performed. We also analyzed transcriptomes of liver tissues collected from mice on a choline-deficient high-fat diet, which developed chronic liver inflammation and tumors, orally given aspirin and clopidogrel or the anti-inflammatory agent sulindac vs mice on a chow (control) diet. Results: We found the ICF gene expression pattern in 50% of liver tissues from patients with cirrhosis without HCC and in 60% of nontumor liver tissues from patients with early-stage HCC. The liver tissues with the ICF gene expression pattern had 3 different features: increased numbers of effector T cells; increased expression of genes that suppress the immune response and activation of transforming growth factor β signaling; or expression of genes that promote inflammation and activation of interferon gamma signaling. Patients with cirrhosis and liver tissues with the immunosuppressive profile (10% of cases) had a higher risk of HCC (hazard ratio, 2.41; 95% confidence interval, 1.21-4.80). Mice with chemically induced fibrosis or diet-induced steatohepatitis given nintedanib or aspirin and clopidogrel down-regulated the ICF gene expression pattern in liver and developed fewer and smaller tumors than mice given vehicle. Conclusions: We identified an immune-related gene expression pattern in liver tissues of patients with early-stage HCC, called the ICF, that is associated with risk of HCC development in patients with cirrhosis. Administration of nintedanib or aspirin and clopidogrel to mice with chronic liver inflammation caused loss of this gene expression pattern and development of fewer and smaller liver tumors. Agents that alter immune regulatory gene expression patterns associated with carcinogenesis might be tested as chemopreventive agents in patients with cirrhosis
Charge Form Factor and Cluster Structure of Li Nucleus
The charge form factor of Li nucleus is considered on the basis of its
cluster structure. The charge density of Li is presented as a
superposition of two terms. One of them is a folded density and the second one
is a sum of He and the deuteron densities. Using the available
experimental data for He and deuteron charge form factors, a good
agreement of the calculations within the suggested scheme is obtained with the
experimental data for the charge form factor of Li, including those in
the region of large transferred momenta.Comment: 12 pages 5 figure
Bessel Process and Conformal Quantum Mechanics
Different aspects of the connection between the Bessel process and the
conformal quantum mechanics (CQM) are discussed. The meaning of the possible
generalizations of both models is investigated with respect to the other model,
including self adjoint extension of the CQM. Some other generalizations such as
the Bessel process in the wide sense and radial Ornstein- Uhlenbeck process are
discussed with respect to the underlying conformal group structure.Comment: 28 Page
A transcribed enhancer dictates mesendoderm specification in pluripotency.
Enhancers and long noncoding RNAs (lncRNAs) are key determinants of lineage specification during development. Here, we evaluate remodeling of the enhancer landscape and modulation of the lncRNA transcriptome during mesendoderm specification. We sort mesendodermal progenitors from differentiating embryonic stem cells (ESCs) according to Eomes expression, and find that enhancer usage is coordinated with mesendoderm-specific expression of key lineage-determining transcription factors. Many of these enhancers are associated with the expression of lncRNAs. Examination of ESC-specific enhancers interacting in three-dimensional space with mesendoderm-specifying transcription factor loci identifies MesEndoderm Transcriptional Enhancer Organizing Region (Meteor). Genetic and epigenetic manipulation of the Meteor enhancer reveal its indispensable role during mesendoderm specification and subsequent cardiogenic differentiation via transcription-independent and -dependent mechanisms. Interestingly, Meteor-deleted ESCs are epigenetically redirected towards neuroectodermal lineages. Loci, topologically associating a transcribed enhancer and its cognate protein coding gene, appear to represent therefore a class of genomic elements controlling developmental competence in pluripotency
Oxidised cosmic acceleration
We give detailed proofs of several new no-go theorems for constructing flat
four-dimensional accelerating universes from warped dimensional reduction.
These new theorems improve upon previous ones by weakening the energy
conditions, by including time-dependent compactifications, and by treating
accelerated expansion that is not precisely de Sitter. We show that de Sitter
expansion violates the higher-dimensional null energy condition (NEC) if the
compactification manifold M is one-dimensional, if its intrinsic Ricci scalar R
vanishes everywhere, or if R and the warp function satisfy a simple limit
condition. If expansion is not de Sitter, we establish threshold
equation-of-state parameters w below which accelerated expansion must be
transient. Below the threshold w there are bounds on the number of e-foldings
of expansion. If M is one-dimensional or R everywhere vanishing, exceeding the
bound implies the NEC is violated. If R does not vanish everywhere on M,
exceeding the bound implies the strong energy condition (SEC) is violated.
Observationally, the w thresholds indicate that experiments with finite
resolution in w can cleanly discriminate between different models which satisfy
or violate the relevant energy conditions.Comment: v2: corrections, references adde
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