1,466 research outputs found
What\u27s An Intimate Relationship, Anyway? Expanding Access to the New York State Family Courts for Civil Orders of Protection
Comment on ``Protective measurements of the wave function of a single squeezed harmonic-oscillator state''
Alter and Yamamoto [Phys. Rev. A 53, R2911 (1996)] claimed to consider
``protective measurements'' [Phys. Lett. A 178, 38 (1993)] which we have
recently introduced. We show that the measurements discussed by Alter and
Yamamoto ``are not'' the protective measurements we proposed. Therefore, their
results are irrelevant to the nature of protective measurements.Comment: 2 pages LaTe
The Iterative Signature Algorithm for the analysis of large scale gene expression data
We present a new approach for the analysis of genome-wide expression data.
Our method is designed to overcome the limitations of traditional techniques,
when applied to large-scale data. Rather than alloting each gene to a single
cluster, we assign both genes and conditions to context-dependent and
potentially overlapping transcription modules. We provide a rigorous definition
of a transcription module as the object to be retrieved from the expression
data. An efficient algorithm, that searches for the modules encoded in the data
by iteratively refining sets of genes and conditions until they match this
definition, is established. Each iteration involves a linear map, induced by
the normalized expression matrix, followed by the application of a threshold
function. We argue that our method is in fact a generalization of Singular
Value Decomposition, which corresponds to the special case where no threshold
is applied. We show analytically that for noisy expression data our approach
leads to better classification due to the implementation of the threshold. This
result is confirmed by numerical analyses based on in-silico expression data.
We discuss briefly results obtained by applying our algorithm to expression
data from the yeast S. cerevisiae.Comment: Latex, 36 pages, 8 figure
Macrostate Data Clustering
We develop an effective nonhierarchical data clustering method using an
analogy to the dynamic coarse graining of a stochastic system. Analyzing the
eigensystem of an interitem transition matrix identifies fuzzy clusters
corresponding to the metastable macroscopic states (macrostates) of a diffusive
system. A "minimum uncertainty criterion" determines the linear transformation
from eigenvectors to cluster-defining window functions. Eigenspectrum gap and
cluster certainty conditions identify the proper number of clusters. The
physically motivated fuzzy representation and associated uncertainty analysis
distinguishes macrostate clustering from spectral partitioning methods.
Macrostate data clustering solves a variety of test cases that challenge other
methods.Comment: keywords: cluster analysis, clustering, pattern recognition, spectral
graph theory, dynamic eigenvectors, machine learning, macrostates,
classificatio
Patterns of subnet usage reveal distinct scales of regulation in the transcriptional regulatory network of Escherichia coli
The set of regulatory interactions between genes, mediated by transcription
factors, forms a species' transcriptional regulatory network (TRN). By
comparing this network with measured gene expression data one can identify
functional properties of the TRN and gain general insight into transcriptional
control. We define the subnet of a node as the subgraph consisting of all nodes
topologically downstream of the node, including itself. Using a large set of
microarray expression data of the bacterium Escherichia coli, we find that the
gene expression in different subnets exhibits a structured pattern in response
to environmental changes and genotypic mutation. Subnets with less changes in
their expression pattern have a higher fraction of feed-forward loop motifs and
a lower fraction of small RNA targets within them. Our study implies that the
TRN consists of several scales of regulatory organization: 1) subnets with more
varying gene expression controlled by both transcription factors and
post-transcriptional RNA regulation, and 2) subnets with less varying gene
expression having more feed-forward loops and less post-transcriptional RNA
regulation.Comment: 14 pages, 8 figures, to be published in PLoS Computational Biolog
A Novel Unsupervised Method to Identify Genes Important in the Anti-viral Response: Application to Interferon/Ribavirin in Hepatitis C Patients
Background: Treating hepatitis C with interferon/ribavirin results in a varied response in terms of decrease in viral titer and ultimate outcome. Marked responders have a sharp decline in viral titer within a few days of treatment initiation, whereas in other patients there is no effect on the virus (poor responders). Previous studies have shown that combination therapy modifies expression of hundreds of genes in vitro and in vivo. However, identifying which, if any, of these genes have a role in viral clearance remains challenging. Aims: The goal of this paper is to link viral levels with gene expression and thereby identify genes that may be responsible for early decrease in viral titer. Methods: Microarrays were performed on RNA isolated from PBMC of patients undergoing interferon/ribavirin therapy. Samples were collected at pre-treatment (day 0), and 1, 2, 7, 14 and 28 days after initiating treatment. A novel method was applied to identify genes that are linked to a decrease in viral titer during interferon/ribavirin treatment. The method uses the relationship between inter-patient gene expression based proximities and inter-patient viral titer based proximities to define the association between microarray gene expression measurements of each gene and viral-titer measurements. Results: We detected 36 unique genes whose expressions provide a clustering of patients that resembles viral titer based clustering of patients. These genes include IRF7, MX1, OASL and OAS2, viperin and many ISG's of unknown function. Conclusion: The genes identified by this method appear to play a major role in the reduction of hepatitis C virus during the early phase of treatment. The method has broad utility and can be used to analyze response to any group of factors influencing biological outcome such as antiviral drugs or anti-cancer agents where microarray data are available. © 2007 Brodsky et al
Fidelity trade-off for finite ensembles of identically prepared qubits
We calculate the trade-off between the quality of estimating the quantum
state of an ensemble of identically prepared qubits and the minimum level of
disturbance that has to be introduced by this procedure in quantum mechanics.
The trade-off is quantified using two mean fidelities: the operation fidelity
which characterizes the average resemblance of the final qubit state to the
initial one, and the estimation fidelity describing the quality of the obtained
estimate. We analyze properties of quantum operations saturating the
achievability bound for the operation fidelity versus the estimation fidelity,
which allows us to reduce substantially the complexity of the problem of
finding the trade-off curve. The reduced optimization problem has the form of
an eigenvalue problem for a set of tridiagonal matrices, and it can be easily
solved using standard numerical tools.Comment: 26 pages, REVTeX, 2 figures. Few minor corrections, accepted for
publication in Physical Review
The Escherichia coli transcriptome mostly consists of independently regulated modules
Underlying cellular responses is a transcriptional regulatory network (TRN) that modulates gene expression. A useful description of the TRN would decompose the transcriptome into targeted effects of individual transcriptional regulators. Here, we apply unsupervised machine learning to a diverse compendium of over 250 high-quality Escherichia coli RNA-seq datasets to identify 92 statistically independent signals that modulate the expression of specific gene sets. We show that 61 of these transcriptomic signals represent the effects of currently characterized transcriptional regulators. Condition-specific activation of signals is validated by exposure of E. coli to new environmental conditions. The resulting decomposition of the transcriptome provides: a mechanistic, systems-level, network-based explanation of responses to environmental and genetic perturbations; a guide to gene and regulator function discovery; and a basis for characterizing transcriptomic differences in multiple strains. Taken together, our results show that signal summation describes the composition of a model prokaryotic transcriptome
Exploring leadership in multi-sectoral partnerships
This article explores some critical aspects of leadership in the context of multi-sectoral partnerships. It focuses on leadership in practice and asks the question, `How do managers experience and perceive leadership in such partnerships?' The study contributes to the debate on whether leadership in a multi-sectoral partnership context differs from that within a single organization. It is based on the accounts of practising managers working in complex partnerships. The article highlights a number of leadership challenges faced by those working in multi-sectoral partnerships. Partnership practitioners were clear that leadership in partnerships was more complex than in single organizations. However, it was more difficult for them to agree a consensus on the essential nature of leadership in partnership. We suggest that a first-, second- and third-person approach might be a way of better interpreting leadership in the context of partnerships
The noise in gravitational-wave detectors and other classical-force measurements is not influenced by test-mass quantization
It is shown that photon shot noise and radiation-pressure back-action noise
are the sole forms of quantum noise in interferometric gravitational wave
detectors that operate near or below the standard quantum limit, if one filters
the interferometer output appropriately. No additional noise arises from the
test masses' initial quantum state or from reduction of the test-mass state due
to measurement of the interferometer output or from the uncertainty principle
associated with the test-mass state. Two features of interferometers are
central to these conclusions: (i) The interferometer output (the photon number
flux N(t) entering the final photodetector) commutes with itself at different
times in the Heisenberg Picture, [N(t), N(t')] = 0, and thus can be regarded as
classical. (ii) This number flux is linear in the test-mass initial position
and momentum operators x_o and p_o, and those operators influence the measured
photon flux N(t) in manners that can easily be removed by filtering -- e.g., in
most interferometers, by discarding data near the test masses' 1 Hz swinging
freqency. The test-mass operators x_o and p_o contained in the unfiltered
output N(t) make a nonzero contribution to the commutator [N(t), N(t')]. That
contribution is cancelled by a nonzero commutation of the photon shot noise and
radiation-pressure noise, which also are contained in N(t). This cancellation
of commutators is responsible for the fact that it is possible to derive an
interferometer's standard quantum limit from test-mass considerations, and
independently from photon-noise considerations. These conclusions are true for
a far wider class of measurements than just gravitational-wave interferometers.
To elucidate them, this paper presents a series of idealized thought
experiments that are free from the complexities of real measuring systems.Comment: Submitted to Physical Review D; Revtex, no figures, prints to 14
pages. Second Revision 1 December 2002: minor rewording for clarity,
especially in Sec. II.B.3; new footnote 3 and passages before Eq. (2.35) and
at end of Sec. III.B.
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