128 research outputs found
The Theory of the Interleaving Distance on Multidimensional Persistence Modules
In 2009, Chazal et al. introduced -interleavings of persistence
modules. -interleavings induce a pseudometric on (isomorphism
classes of) persistence modules, the interleaving distance. The definitions of
-interleavings and generalize readily to multidimensional
persistence modules. In this paper, we develop the theory of multidimensional
interleavings, with a view towards applications to topological data analysis.
We present four main results. First, we show that on 1-D persistence modules,
is equal to the bottleneck distance . This result, which first
appeared in an earlier preprint of this paper, has since appeared in several
other places, and is now known as the isometry theorem. Second, we present a
characterization of the -interleaving relation on multidimensional
persistence modules. This expresses transparently the sense in which two
-interleaved modules are algebraically similar. Third, using this
characterization, we show that when we define our persistence modules over a
prime field, satisfies a universality property. This universality result
is the central result of the paper. It says that satisfies a stability
property generalizing one which is known to satisfy, and that in
addition, if is any other pseudometric on multidimensional persistence
modules satisfying the same stability property, then . We also show
that a variant of this universality result holds for , over arbitrary
fields. Finally, we show that restricts to a metric on isomorphism
classes of finitely presented multidimensional persistence modules.Comment: Major revision; exposition improved throughout. To appear in
Foundations of Computational Mathematics. 36 page
RNAG: a new Gibbs sampler for predicting RNA secondary structure for unaligned sequences
Motivation: RNA secondary structure plays an important role in the function of many RNAs, and structural features are often key to their interaction with other cellular components. Thus, there has been considerable interest in the prediction of secondary structures for RNA families. In this article, we present a new global structural alignment algorithm, RNAG, to predict consensus secondary structures for unaligned sequences. It uses a blocked Gibbs sampling algorithm, which has a theoretical advantage in convergence time. This algorithm iteratively samples from the conditional probability distributions P(Structure | Alignment) and P(Alignment | Structure). Not surprisingly, there is considerable uncertainly in the high-dimensional space of this difficult problem, which has so far received limited attention in this field. We show how the samples drawn from this algorithm can be used to more fully characterize the posterior space and to assess the uncertainty of predictions
Landholder Typologies Used in the Development of Natural Resource Management Programs in Australia - A Review
This article reviews the literature on the identification of landholder typologies that can be used to assist the design and delivery of natural resource management (NRM) programs. Australian researchers have developed typologies of landholders based on a variety of criteria. The rationale for developing landholder typologies is first discussed before reviewing the various approaches that have been used by Australian researchers and comparing their findings. The methods employed have differed according to the theories used to guide the research and the 'clients' or 'sponsors' of the research. The landholder types they describe, however, have a number of similarities. These similarities suggest that the studies have identified the same fundamental divisions in the rural community, and that it may be possible to integrate landholder typologies for a variety of NRM and non-NRM applications. It is concluded that further research could usefully investigate whether concepts of social class or sub-cultures may be appropriate to define and describe the variations in landholder types
Trihydrophobin 1 Phosphorylation by c-Src Regulates MAPK/ERK Signaling and Cell Migration
c-Src activates Ras-MAPK/ERK signaling pathway and regulates cell migration, while trihydrophobin 1 (TH1) inhibits MAPK/ERK activation and cell migration through interaction with A-Raf and PAK1 and inhibiting their kinase activities. Here we show that c-Src interacts with TH1 by GST-pull down assay, coimmunoprecipitation and confocal microscopy assay. The interaction leads to phosphorylation of TH1 at Tyr-6 in vivo and in vitro. Phosphorylation of TH1 decreases its association with A-Raf and PAK1. Further study reveals that Tyr-6 phosphorylation of TH1 reduces its inhibition on MAPK/ERK signaling, enhances c-Src mediated cell migration. Moreover, induced tyrosine phosphorylation of TH1 has been found by EGF and estrogen treatments. Taken together, our findings demonstrate a novel mechanism for the comprehensive regulation of Ras/Raf/MEK/ERK signaling and cell migration involving tyrosine phosphorylation of TH1 by c-Src
Inhibition of cancer cell invasion and metastasis by genistein
Genistein is a small, biologically active flavonoid that is found in high amounts in soy. This important compound possesses a wide variety of biological activities, but it is best known for its ability to inhibit cancer progression. In particular, genistein has emerged as an important inhibitor of cancer metastasis. Consumption of genistein in the diet has been linked to decreased rates of metastatic cancer in a number of population-based studies. Extensive investigations have been performed to determine the molecular mechanisms underlying genisteinβs antimetastatic activity, with results indicating that this small molecule has significant inhibitory activity at nearly every step of the metastatic cascade. Reports have demonstrated that, at high concentrations, genistein can inhibit several proteins involved with primary tumor growth and apoptosis, including the cyclin class of cell cycle regulators and the Akt family of proteins. At lower concentrations that are similar to those achieved through dietary consumption, genistein can inhibit the prometastatic processes of cancer cell detachment, migration, and invasion through a variety of mechanisms, including the transforming growth factor (TGF)-Ξ² signaling pathway. Several in vitro findings have been corroborated in both in vivo animal studies and in early-phase human clinical trials, demonstrating that genistein can both inhibit human cancer metastasis and also modulate markers of metastatic potential in humans, respectively. Herein, we discuss the variety of mechanisms by which genistein regulates individual steps of the metastatic cascade and highlight the potential of this natural product as a promising therapeutic inhibitor of metastasis
Transformations on tensor products and the torsionless property in abelian groups: Corrigendum
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