15,653 research outputs found
OGSA/Globus Evaluation for Data Intensive Applications
We present an architecture of Globus Toolkit 3 based testbed intended for
evaluation of applicability of the Open Grid Service Architecture (OGSA) for
Data Intensive Applications.Comment: To be published in the proceedings of the XIX International Symposium
on Nuclear Electronics and Computing (NEC'2003), Bulgaria, Varna, 15-20
September, 200
Network growth models and genetic regulatory networks
We study a class of growth algorithms for directed graphs that are candidate
models for the evolution of genetic regulatory networks. The algorithms involve
partial duplication of nodes and their links, together with innovation of new
links, allowing for the possibility that input and output links from a newly
created node may have different probabilities of survival. We find some
counterintuitive trends as parameters are varied, including the broadening of
indegree distribution when the probability for retaining input links is
decreased. We also find that both the scaling of transcription factors with
genome size and the measured degree distributions for genes in yeast can be
reproduced by the growth algorithm if and only if a special seed is used to
initiate the process.Comment: 8 pages with 7 eps figures; uses revtex4. Added references, cleaner
figure
Investigation of Pressure Distribution over an Extended Leading-Edge Flap on a 42 Degrees Sweptback Wing
Pressure distribution over an extended leading-edge flap on a 42 degree swept-back wing was investigated. Results indicate that the flap normal-force coefficient increased almost linearly with the angle of attack to a maximum value of 3.25. The maximum section normal-force coefficient was located about 30 percent of the flap span outboard of the inboard end and had a value of 3.75. Peak negative pressures built up at the flap leading edge as the angle of attack was increased and caused the chordwise location of the flap center of pressure to be move forward
Use of high throughput sequencing to observe genome dynamics at a single cell level
With the development of high throughput sequencing technology, it becomes
possible to directly analyze mutation distribution in a genome-wide fashion,
dissociating mutation rate measurements from the traditional underlying
assumptions. Here, we sequenced several genomes of Escherichia coli from
colonies obtained after chemical mutagenesis and observed a strikingly
nonrandom distribution of the induced mutations. These include long stretches
of exclusively G to A or C to T transitions along the genome and orders of
magnitude intra- and inter-genomic differences in mutation density. Whereas
most of these observations can be explained by the known features of enzymatic
processes, the others could reflect stochasticity in the molecular processes at
the single-cell level. Our results demonstrate how analysis of the molecular
records left in the genomes of the descendants of an individual mutagenized
cell allows for genome-scale observations of fixation and segregation of
mutations, as well as recombination events, in the single genome of their
progenitor.Comment: 22 pages, 9 figures (including 5 supplementary), one tabl
Correlations of record events as a test for heavy-tailed distributions
A record is an entry in a time series that is larger or smaller than all
previous entries. If the time series consists of independent, identically
distributed random variables with a superimposed linear trend, record events
are positively (negatively) correlated when the tail of the distribution is
heavier (lighter) than exponential. Here we use these correlations to detect
heavy-tailed behavior in small sets of independent random variables. The method
consists of converting random subsets of the data into time series with a
tunable linear drift and computing the resulting record correlations.Comment: Revised version, to appear in Physical Review Letter
Examining c-di-GMP and possible quorum sensing regulation in Pseudomonas fluorescens SBW25:links between intra and inter-cellular regulation benefits community cooperative activities such as biofilm formation
Bacterial success in colonizing complex environments requires individual response to micro-scale conditions as well as community-level cooperation to produce large-scale structures such as biofilms. Connecting individual and community responses could be achieved by linking the intracellular sensory and regulatory systems mediated by bis-(3β²-5β²)-cyclic dimeric guanosine monophosphate (c-di-GMP) and other compounds of individuals with intercellular quorum sensing (QS) regulation controlling populations. There is growing evidence to suggest that biofilm formation by many pseudomonads is regulated by both intra and intercellular systems, though in the case of the model Pseudomonas fluorescens SBW25 Wrinkly Spreader in which mutations increasing c-di-GMP levels result in the production of a robust cellulose-based air-liquid interface biofilm, no evidence for the involvement of QS regulation has been reported. However, our recent review of the P. fluorescens SBW25 genome has identified a potential QS regulatory pathway and other QSβassociated genes linked to c-di-GMP homeostasis, and QS signal molecules have also been identified in culture supernatants. These findings suggest a possible link between c-di-GMP and QS regulation in P. fluorescens SBW25 which might allow a more sophisticated and responsive control of cellulose production and biofilm formation when colonising the soil and plant-associated environments P. fluorescens SBW25 normally inhabits.ΠΠ½Π°Π»ΠΈΠ· Ρ-Π΄ΠΈ-ΠΠΠ€ ΠΈ Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΠΎΠ³ΠΎ ΡΡΠ²ΡΡΠ²Π° ΠΊΠ²ΠΎΡΡΠΌΠ° Ρ Pseudomonas fluorescens SBW 25: ΡΠ²ΡΠ·Ρ ΠΌΠ΅ΠΆΠ΄Ρ Π²Π½ΡΡΡΠΈ ΠΈ ΠΌΠ΅ΠΆΠΊΠ»Π΅ΡΠΎΡΠ½ΠΎΠΉ ΡΠ΅Π³ΡΠ»ΡΡΠΈΠ΅ΠΉ ΡΠΏΠΎΡΠΎΠ±ΡΡΠ²ΡΠ΅Ρ ΠΊΠΎΠΎΠΏΠ΅ΡΠ°ΡΠΈΠ²Π½ΠΎΠΌΡ ΠΏΠΎΠ²Π΅Π΄Π΅Π½ΠΈΡ Π² ΡΠΎΠΎΠ±ΡΠ΅ΡΡΠ²Π΅ ΠΈ ΡΠΎΡΠΌΠΈΡΠΎΠ²Π°Π½ΠΈΡ Π±ΠΈΠΎΠΏΠ»ΡΠ½ΠΊΠΈΠ£ΡΠΏΠ΅ΡΠ½ΠΎΡΡΡ Π±Π°ΠΊΡΠ΅ΡΠΈΠ°Π»ΡΠ½ΠΎΠΉ ΠΊΠΎΠ»ΠΎΠ½ΠΈΠ·Π°ΡΠΈΠΈ ΡΠ»ΠΎΠΆΠ½ΡΡ
ΡΠΊΠΎΠ½ΠΈΡ ΡΡΠ΅Π±ΡΠ΅Ρ ΠΈΠ½Π΄ΠΈΠ²ΠΈΠ΄ΡΠ°Π»ΡΠ½ΠΎΠ³ΠΎ ΠΎΡΠ²Π΅ΡΠ° Π½Π° ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΡ ΡΡΠ»ΠΎΠ²ΠΈΠΉ Π½Π° ΠΌΠΈΠΊΡΠΎΡΡΠΎΠ²Π½Π΅ ΡΠ°Π²Π½ΠΎ ΠΊΠ°ΠΊ ΠΈ ΠΊΠΎΠΎΠΏΠ΅ΡΠ°ΡΠΈΠΈ Π½Π° ΡΡΠΎΠ²Π½Π΅ ΡΠΎΠΎΠ±ΡΠ΅ΡΡΠ²Π° Π΄Π»Ρ ΠΏΡΠΎΠ΄ΡΠΊΡΠΈΠΈ ΡΠ°ΠΊΠΈΡ
ΠΊΡΡΠΏΠ½ΠΎ ΠΌΠ°ΡΡΡΠ°Π±Π½ΡΡ
ΡΡΡΡΠΊΡΡΡ ΠΊΠ°ΠΊ Π±ΠΈΠΎΠΏΠ»ΡΠ½ΠΊΠΈ. ΠΠΎΠΎΡΠ΄ΠΈΠ½Π°ΡΠΈΡ ΠΈΠ½Π΄ΠΈΠ²ΠΈΠ΄ΡΠ°Π»ΡΠ½ΡΡ
ΠΎΡΠ²Π΅Ρ ΠΎΠ² ΠΈ ΠΎΡΠ²Π΅ΡΠΎΠ² ΡΠΎΠΎΠ±ΡΠ΅ΡΡΠ²Π° ΠΌΠΎΠΆΠ΅Ρ Π±ΡΡΡ Π΄ΠΎΡΡΠΈΠ³Π½ΡΡΠ° ΠΏΡΡΠ΅ΠΌ ΡΠ²ΡΠ·ΡΠ²Π°Π½ΠΈΡ Π²Π½ΡΡΡΠΈΠΊΠ»Π΅ΡΠΎΡΠ½ΡΡ
ΡΠ΅Π½ΡΠΎΡΠ½ΡΡ
ΠΈ ΡΠ΅Π³ΡΠ»ΡΡΠΎΡΠ½ΡΡ
ΡΠΈΡΡΠ΅ΠΌ, ΠΎΠΏΠΎΡΡΠ΅Π΄ΡΠ΅ΠΌΡΡ
Π±ΠΈΡ-(3',5')-ΡΠΈΠΊΠ»ΠΈΡΠ΅ΡΠΊΠΈΠΌ Π΄ΠΈΠΌΠ΅ΡΠ½ΡΠΌ Π³ΡΠ°Π½ΠΎΠ·ΠΈΠ½ΠΌΠΎΠ½ΠΎΡΠΎΡΡΠ°ΡΠΎΠΌ (Ρ-Π΄ΠΈ-ΠΠΠ€) ΠΈ Π΄ΡΡΠ³ΠΈΠΌΠΈ ΡΠΎΠ΅Π΄ΠΈΠ½Π΅Π½ΠΈΡΠΌΠΈ ΠΈΠ½Π΄ΠΈΠ²ΠΈΠ΄ΡΡΠΌΠΎΠ² Ρ ΠΌΠ΅ΠΆΠΊΠ»Π΅ΡΠΎΡΠ½ΠΎΠΉ ΡΠ΅Π³ΡΠ»ΡΡΠΈΠ΅ΠΉ - ΡΡΠ²ΡΡΠ²ΠΎΠΌ ΠΊΠ²ΠΎΡΡΠΌΠ° (Π§Π), ΠΊΠΎΠ½ΡΡΠΎΠ»ΠΈΡΡΡΡΠ΅ΠΌ ΠΏΠΎΠΏΡΠ»ΡΡΠΈ Ρ. ΠΠ°ΠΊΠ°ΠΏΠ»ΠΈΠ²Π°Π΅ΡΡΡ Π²ΡΡ Π±ΠΎΠ»ΡΡΠ΅ Π΄ΠΎΠΊΠ°Π·Π°ΡΠ΅Π»ΡΡΡΠ² ΡΠΎΠ³ΠΎ, ΡΡΠΎ ΡΠΎΡΠΌΠΈΡΠΎΠ²Π°Π½ΠΈΠ΅ Π±ΠΈΠΎΠΏΠ»Π΅Π½ΠΊΠΈ ΠΌΠ½ΠΎΠ³ΠΈΠΌΠΈ ΠΏΡΠ΅Π²Π΄ΠΎΠΌΠΎΠ½Π°Π΄Π°ΠΌΠΈ ΡΠ΅Π³ΡΠ»ΠΈΡΡΠ΅ΡΡΡ ΠΊΠ°ΠΊ Π²Π½ΡΡΡΠΈ ΠΊΠ»Π΅ΡΠΎΡΠ½ΡΠΌΠΈ, ΡΠ°ΠΊ ΠΈ ΠΌΠ΅ΠΆ ΠΊΠ»Π΅ΡΠΎΡΠ½ΡΠΌΠΈ ΡΠ΅Π³ΡΠ»ΡΡΠΎΡΠ½ΡΠΌΠΈ ΡΠΈΡΡΠ΅ΠΌΠ°ΠΌΠΈ, Ρ
ΠΎΡΡ Π² ΡΠ»ΡΡΠ°Π΅ ΠΌΠΎΠ΄Π΅Π»ΡΠ½ΠΎΠΉ Pseudomonas fluorescens SBW25 Wrinkly Spreader, Ρ ΠΊΠΎΡΠΎΡΠΎΠΉ ΠΌΡΡΠ°ΡΠΈΠΈ, ΠΏΠΎΠ²ΡΡΠ°ΡΡ ΠΈΠ΅ ΡΡΠΎΠ²Π½ΠΈ Ρ-Π΄ΠΈ-ΠΠΠ€, ΠΏΡΠΈΠ²ΠΎΠ΄ΡΡ ΠΊ ΡΠΎΠ·Π΄Π°Π½ΠΈΡ ΠΏΡΠΎΡΠ½ΠΎΠΉ ΡΠ΅Π»Π»ΡΠ»ΠΎΠ·Π½ΠΎΠΉ Π±ΠΈΠΎΠΏΠ»ΡΠ½ΠΊΠΈ Π½Π° Π³ΡΠ°Π½ΠΈΡΠ΅ ΡΠ°Π·Π΄Π΅Π»Π° ΡΠ°Π· Π²ΠΎΠ·Π΄ΡΡ
-ΠΆΠΈΠ΄ΠΊΠΎΡΡΡ, Π½Π΅ Π±ΡΠ»ΠΎ ΠΎΠ±Π½Π°ΡΡΠΆΠ΅Π½ΠΎ Π½ΠΈ ΠΊΠ° ΠΊΠΎΠ³ΠΎ ΡΠ²ΠΈΠ΄Π΅ΡΠ΅Π»ΡΡΡΠ²Π° Π²ΠΎΠ²Π»Π΅ΡΠ΅Π½ΠΈΡ ΠΊΠ²ΠΎΡΡΠΌ-Π·Π°Π²ΠΈΡΠΈΠΌΠΎΠΉ ΡΠ΅Π³ΡΠ»ΡΡΠΈΠΈ. ΠΠ΄Π½Π°ΠΊΠΎ Π½Π°Ρ Π½Π΅Π΄Π°Π²Π½ΠΈΠΉ ΠΎΠ±Π·ΠΎΡ Π³Π΅Π½ΠΎΠΌΠ° P. fluorescens SBW25 Π²ΡΡΠ²ΠΈΠ» ΠΏΠΎΡΠ΅Π½ΡΠΈΠ°Π»ΡΠ½ΡΠΉ Π§Π-Π·Π°Π²ΠΈΡΠΈΠΌΡΠΉ ΡΠ΅Π³ΡΠ»ΡΡΠΎΡΠ½ΡΠΉ ΠΏΡ ΡΡ ΠΈ Π΄ΡΡΠ³ΠΈΠ΅ Π§Π-Π·Π°Π²ΠΈΡΠΈΠΌΡΠ΅ Π³Π΅Π½Ρ, ΡΠ²ΡΠ·Π°Π½Π½ΡΠ΅ Ρ Π³ΠΎΠΌΠ΅ΠΎΡΡΠ°Π·ΠΎΠΌ Ρ-Π΄ΠΈ-ΠΠΠ€, Π° ΠΌΠΎΠ»Π΅ΠΊΡΠ»Ρ Π§Π-ΡΠΈΠ³Π½Π°Π»ΠΈΠ½Π³Π° Π±ΡΠ»ΠΈ ΠΈΠ΄Π΅Π½ΡΠΈΡΠΈΡΠΈΡΠΎΠ²Π°Π½Ρ Π² ΠΊΡΠ»ΡΡΡΡΠ΅. ΠΡΠΈ Π΄Π°Π½Π½ΡΠ΅ ΡΠ²ΠΈΠ΄Π΅ΡΠ΅Π»ΡΡΡΠ²ΡΡΡ ΠΎ Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΠΎΠΉ ΡΠ²ΡΠ·ΠΈ ΠΌΠ΅ΠΆΠ΄Ρ Ρ-Π΄ΠΈ-ΠΠΠ€-ΡΠ΅Π³ΡΠ»ΡΡΠΈΠ΅ΠΉ ΠΈ Π§Π Ρ P. fluorescens SBW25, ΡΡΠΎ ΠΏΠΎΠ·Π²ΠΎΠ»ΡΠ΅Ρ Π±ΠΎΠ»Π΅Π΅ ΡΠ»ΠΎΠΆΠ½ΡΠΉ ΠΈ Π³ΠΈΠ±ΠΊΠΈΠΉ ΠΊΠΎΠ½ΡΡΠΎΠ»Ρ Π½Π°Π΄ ΠΏΡΠΎΠ΄ΡΠΊΡΠΈΠ΅ΠΉ ΡΠ΅Π»Π»ΡΠ»ΠΎΠ·Ρ ΠΈ ΠΎΠ±ΡΠ°Π·ΠΎΠ²Π°Π½ΠΈ Π΅ΠΌ Π±ΠΈΠΎΠΏΠ»Π΅Π½ΠΊΠΈ ΠΏΡΠΈ ΠΊΠΎΠ»ΠΎΠ½ΠΈΠ·Π°ΡΠΈΠΈ ΠΏΠΎΡΠ² ΠΈ ΡΠΊΠΎΠ½ΠΈΡ, aΡΡΠΎΡΠΈΠΈΡΠΎΠ²Π°Π½Π½ΡΡ
Ρ ΡΠ°ΡΡΠ΅Π½ΠΈΡΠΌ ΠΈ, - Π΅ΡΡΠ΅ΡΡΠ²Π΅Π½Π½ΡΠΌΠΈ ΡΡΠ΅Π΄Π°ΠΌΠΈ ΠΎΠ±ΠΈΡΠ°Π½ΠΈΡ P. fluorescens SBW25
The Anatomy of a Grid portal
In this paper we introduce a new way to deal with Grid portals referring to
our implementation. L-GRID is a light portal to access the EGEE/EGI Grid
infrastructure via Web, allowing users to submit their jobs from a common Web
browser in a few minutes, without any knowledge about the Grid infrastructure.
It provides the control over the complete lifecycle of a Grid Job, from its
submission and status monitoring, to the output retrieval. The system,
implemented as client-server architecture, is based on the Globus Grid
middleware. The client side application is based on a java applet; the server
relies on a Globus User Interface. There is no need of user registration on the
server side, and the user needs only his own X.509 personal certificate. The
system is user-friendly, secure (it uses SSL protocol, mechanism for dynamic
delegation and identity creation in public key infrastructures), highly
customizable, open source, and easy to install. The X.509 personal certificate
does not get out from the local machine. It allows to reduce the time spent for
the job submission, granting at the same time a higher efficiency and a better
security level in proxy delegation and management.Comment: 6 page
Vortex pairing in two-dimensional Bose gases
Recent experiments on ultracold Bose gases in two dimensions have provided
evidence for the existence of the Berezinskii-Kosterlitz-Thouless (BKT) phase
via analysis of the interference between two independent systems. In this work
we study the two-dimensional quantum degenerate Bose gas at finite temperature
using the projected Gross-Pitaevskii equation classical field method. While
this describes the highly occupied modes of the gas below a momentum cutoff, we
have developed a method to incorporate the higher momentum states in our model.
We concentrate on finite-sized homogeneous systems in order to simplify the
analysis of the vortex pairing. We determine the dependence of the condensate
fraction on temperature and compare this to the calculated superfluid fraction.
By measuring the first order correlation function we determine the boundary of
the Bose-Einstein condensate and BKT phases, and find it is consistent with the
superfluid fraction decreasing to zero. We reveal the characteristic unbinding
of vortex pairs above the BKT transition via a coarse-graining procedure.
Finally, we model the procedure used in experiments to infer system
correlations [Hadzibabic et al., Nature 441, 1118 (2006)], and quantify its
level of agreement with directly calculated in situ correlation functions.Comment: published versio
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