128 research outputs found
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We explore using a moderately sized large language model (GPT-J 6B
parameters) to create a plan for a simulated robot to achieve 30 classes of
goals in ScienceWorld, a text game simulator for elementary science
experiments. Previously published empirical work claimed that large language
models (LLMs) are a poor fit (Wang et al., 2022) compared to reinforcement
learning. Using the Markov assumption (a single previous step), the LLM
outperforms the reinforcement learning-based approach by a factor of 1.4. When
we fill the LLM's input buffer with as many prior steps as possible,
improvement rises to 3.5x. Even when training on only 6.5% of the training
data, we observe a 2.2x improvement over the reinforcement-learning-based
approach. Our experiments show that performance varies widely across the 30
classes of actions, indicating that averaging over tasks can hide significant
performance issues. In work contemporaneous with ours, Lin et al. (2023)
demonstrated a two-part approach (SwiftSage) that uses a small LLM (T5-large)
complemented by OpenAI's massive LLMs to achieve outstanding results in
ScienceWorld. Our 6-B parameter, single-stage GPT-J matches the performance of
SwiftSage's two-stage architecture when it incorporates GPT-3.5 turbo which has
29-times more parameters than GPT-J.Comment: Identical to EMNLP 2023 Finding
Spin dynamics simulations of the magnetic dynamics of RbMnF and direct comparison with experiment
Spin-dynamics techniques have been used to perform large-scale simulations of
the dynamic behavior of the classical Heisenberg antiferromagnet in simple
cubic lattices with linear sizes . This system is widely recognized
as an appropriate model for the magnetic properties of RbMnF.
Time-evolutions of spin configurations were determined numerically from coupled
equations of motion for individual spins using a new algorithm implemented by
Krech {\it etal}, which is based on fourth-order Suzuki-Trotter decompositions
of exponential operators. The dynamic structure factor was calculated from the
space- and time-displaced spin-spin correlation function. The crossover from
hydrodynamic to critical behavior of the dispersion curve and spin-wave
half-width was studied as the temperature was increased towards the critical
temperature. The dynamic critical exponent was estimated to be , which is slightly lower than the dynamic scaling prediction, but in
good agreement with a recent experimental value. Direct, quantitative
comparisons of both the dispersion curve and the lineshapes obtained from our
simulations with very recent experimental results for RbMnF are presented.Comment: 30 pages, RevTex, 9 figures, to appear in PR
The GALEX Ultraviolet Atlas of Nearby Galaxies
We present images, integrated photometry, surface-brightness and color
profiles for a total of 1034 nearby galaxies recently observed by the GALEX
satellite in its far-ultraviolet (FUV; 1516A) and near-ultraviolet (NUV; 2267A)
bands. (...) This data set has been complemented with archival optical,
near-infrared, and far-infrared fluxes and colors. We find that the integrated
(FUV-K) color provides robust discrimination between elliptical and
spiral/irregular galaxies and also among spiral galaxies of different
sub-types. Elliptical galaxies with brighter K-band luminosities (i.e. more
massive) are redder in (NUV-K) color but bluer in (FUV-NUV) than less massive
ellipticals. In the case of the spiral/irregular galaxies our analysis shows
the presence of a relatively tight correlation between the (FUV-NUV) color and
the total infrared-to-UV ratio. The correlation found between (FUV-NUV) color
and K-band luminosity (with lower luminosity objects being bluer than more
luminous ones) can be explained as due to an increase in the dust content with
galaxy luminosity.
The images in this Atlas along with the profiles and integrated properties
are publicly available through a dedicated web page at
http://nedwww.ipac.caltech.edu/level5/GALEX_Atlas/Comment: 181 pages, 10 figures, accepted for publication in ApJS (abstract
abridged
Digital Signal Processing Research Program
Contains table of contents for Section 2, an introduction, reports on twenty-one research projects and a list of publications.U.S. Navy - Office of Naval Research Grant N00014-93-1-0686Lockheed Sanders, Inc. Contract P.O. BY5561U.S. Air Force - Office of Scientific Research Grant AFOSR 91-0034National Science Foundation Grant MIP 95-02885U.S. Navy - Office of Naval Research Grant N00014-95-1-0834MIT-WHOI Joint Graduate Program in Oceanographic EngineeringAT&T Laboratories Doctoral Support ProgramDefense Advanced Research Projects Agency/U.S. Navy - Office of Naval Research Grant N00014-89-J-1489Lockheed Sanders/U.S. Navy - Office of Naval Research Grant N00014-91-C-0125U.S. Navy - Office of Naval Research Grant N00014-89-J-1489National Science Foundation Grant MIP 95-02885Defense Advanced Research Projects Agency/U.S. Navy Contract DAAH04-95-1-0473U.S. Navy - Office of Naval Research Grant N00014-91-J-1628University of California/Scripps Institute of Oceanography Contract 1003-73-5
Ăpisodes dâinactivitĂ© et revenus criminels dans une trajectoire de dĂ©linquance
LâinstabilitĂ© de lâactivitĂ© criminelle dans le temps est dĂ©jĂ bien documentĂ©e. On connaĂźt toutefois
peu les circonstances qui expliquent ces variations Ă court terme. Une meilleure connaissance de
ces facteurs est souhaitable puisquâil est possible que les transitions et les changements Ă court
terme précÚdent les points tournants des carriÚres criminelles. Les conditions qui rendent compte
dâune interruption temporaire des activitĂ©s peuvent, par exemple, contribuer Ă expliquer un
dĂ©sistement dĂ©finitif. LâĂ©tude se fonde sur les trajectoires de 172 dĂ©linquants impliquĂ©s dans des
crimes Ă but lucratif et analyse les variations mensuelles de leurs revenus criminels ainsi que les
Ă©pisodes dâinactivitĂ© criminelle Ă lâintĂ©rieur dâune pĂ©riode fenĂȘtre de 36 mois. La mĂ©thode des
calendriers dâhistoire de vie combinĂ©e aux modĂšles hiĂ©rarchiques permet dâexaminer
conjointement le rÎle de facteurs statiques (les caractéristiques individuelles des sujets) et
dynamiques (les circonstances de vie). Les rĂ©sultats mettent en Ă©vidence lâimportance des
événements qui marquent le style de vie des délinquants et des paramÚtres qui caractérisent
lâengagement criminel dans la comprĂ©hension des variations dans les trajectoires Ă lâĂ©tude. Ils
soulignent Ă©galement lâimportance de la finalitĂ© derriĂšre les activitĂ©s criminelles pour expliquer
la décision des délinquants de cesser temporaire leurs activités illicites
The Toronto prehospital hypertonic resuscitation-head injury and multi organ dysfunction trial (TOPHR HIT) - Methods and data collection tools
<p>Abstract</p> <p>Background</p> <p>Clinical trials evaluating the use of hypertonic saline in the treatment of hypovolemia and head trauma suggest no survival superiority over normal saline; however subgroup analyses suggest there may be a reduction in the inflammatory response and multiorgan failure which may lead to better survival and enhanced neurocognitive function. We describe a feasibility study of randomizing head injured patients to hypertonic saline and dextran vs. normal saline administration in the out of hospital setting.</p> <p>Methods/Design</p> <p>This feasibility study employs a randomized, placebo-controlled design evaluating normal saline compared with a single dose of 250 ml of 7.5% hypertonic saline in 6% dextran 70 in the management of traumatic brain injuries. The primary feasibility endpoints of the trial were: 1) baseline survival rates for the treatment and control group to aid in the design of a definitive multicentre trial, 2) randomization compliance rate, 3) ease of protocol implementation in the out-of-hospital setting, and 4) adverse event rate of HSD infusion.</p> <p>The secondary objectives include measuring the effect of HSD in modulating the immuno-inflammatory response to severe head injury and its effect on modulating the release of neuro-biomarkers into serum; evaluating the role of serum neuro-biomarkers in predicting patient outcome and clinical response to HSD intervention; evaluating effects of HSD on brain atrophy post-injury and neurocognitive and neuropsychological outcomes.</p> <p>Discussion</p> <p>We anticipate three aspects of the trial will present challenges to trial success; ethical demands associated with a waiver of consent trial, challenging follow up and comprehensive accurate timely data collection of patient identifiers and clinical or laboratory values. In addition all the data collection tools had to be derived de novo as none existed in the literature.</p> <p>Trial registration number</p> <p>NCT00878631</p
Thermodynamics of the N = 2* flow
We discuss the thermodynamics of the N = 2*, SU (N) gauge theory at large 't Hooft coupling. The tool we use is the non-extremal deformation of the supergravity solution of Pilch and Warner (PW) [13], dual to N = 4, SU (N) gauge theory softly broken to N = 2. We construct the exact non-extremal solution in five-dimensional gauged supergravity and further uplift it to ten dimensions. Turning to the thermodynamics, we analytically compute the leading correction in m/T to the free energy of the non-extremal D3 branes due to the PW mass deformation, and find that it is positive. We also demonstrate that the mass deformation of the non-extremal D3 brane geometry induces a temperature dependent gaugino condensate. We find that the standard procedure of extracting the N = 2* gauge theory thermodynamic quantities from the dual supergravity leads to a violation of the first law of thermodynamics. We speculate on a possible resolution of this paradox.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/49141/2/jhep112003031.pd
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Genome-wide association studies (GWAS) have identified >300 loci associated with measures of adiposity including body mass index (BMI) and waist-to-hip ratio (adjusted for BMI, WHRadjBMI), but few have been identified through screening of the African ancestry genomes. We performed large scale meta-analyses and replications in up to 52,895 individuals for BMI and up to 23,095 individuals for WHRadjBMI from the African Ancestry Anthropometry Genetics Consortium (AAAGC) using 1000 Genomes phase 1 imputed GWAS to improve coverage of both common and low frequency variants in the low linkage disequilibrium African ancestry genomes. In the sex-combined analyses, we identified one novel locus (TCF7L2/HABP2) for WHRadjBMI and eight previously established loci at P < 5Ă10â8: seven for BMI, and one for WHRadjBMI in African ancestry individuals. An additional novel locus (SPRYD7/DLEU2) was identified for WHRadjBMI when combined with European GWAS. In the sex-stratified analyses, we identified three novel loci for BMI (INTS10/LPL and MLC1 in men, IRX4/IRX2 in women) and four for WHRadjBMI (SSX2IP, CASC8, PDE3B and ZDHHC1/HSD11B2 in women) in individuals of African ancestry or both African and European ancestry. For four of the novel variants, the minor allele frequency was low (<5%). In the trans-ethnic fine mapping of 47 BMI loci and 27 WHRadjBMI loci that were locus-wide significant (P < 0.05 adjusted for effective number of variants per locus) from the African ancestry sex-combined and sex-stratified analyses, 26 BMI loci and 17 WHRadjBMI loci contained †20 variants in the credible sets that jointly account for 99% posterior probability of driving the associations. The lead variants in 13 of these loci had a high probability of being causal. As compared to our previous HapMap imputed GWAS for BMI and WHRadjBMI including up to 71,412 and 27,350 African ancestry individuals, respectively, our results suggest that 1000 Genomes imputation showed modest improvement in identifying GWAS loci including low frequency variants. Trans-ethnic meta-analyses further improved fine mapping of putative causal variants in loci shared between the African and European ancestry populations
Genetic diversity fuels gene discovery for tobacco and alcohol use
Tobacco and alcohol use are heritable behaviours associated with 15% and 5.3% of worldwide deaths, respectively, due largely to broad increased risk for disease and injury(1-4). These substances are used across the globe, yet genome-wide association studies have focused largely on individuals of European ancestries(5). Here we leveraged global genetic diversity across 3.4 million individuals from four major clines of global ancestry (approximately 21% non-European) to power the discovery and fine-mapping of genomic loci associated with tobacco and alcohol use, to inform function of these loci via ancestry-aware transcriptome-wide association studies, and to evaluate the genetic architecture and predictive power of polygenic risk within and across populations. We found that increases in sample size and genetic diversity improved locus identification and fine-mapping resolution, and that a large majority of the 3,823 associated variants (from 2,143 loci) showed consistent effect sizes across ancestry dimensions. However, polygenic risk scores developed in one ancestry performed poorly in others, highlighting the continued need to increase sample sizes of diverse ancestries to realize any potential benefit of polygenic prediction.Peer reviewe
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