601 research outputs found
Tensor hypercontraction: A universal technique for the resolution of matrix elements of local, finite-range -body potentials in many-body quantum problems
Configuration-space matrix elements of N-body potentials arise naturally and
ubiquitously in the Ritz-Galerkin solution of many-body quantum problems. For
the common specialization of local, finite-range potentials, we develop the
eXact Tensor HyperContraction (X-THC) method, which provides a quantized
renormalization of the coordinate-space form of the N-body potential, allowing
for a highly separable tensor factorization of the configuration-space matrix
elements. This representation allows for substantial computational savings in
chemical, atomic, and nuclear physics simulations, particularly with respect to
difficult "exchange-like" contractions.Comment: Third version of the manuscript after referee's comments. In press in
PRL. Main text: 4 pages, 2 figures, 1 table; Supplemental material (also
included): 14 pages, 2 figures, 2 table
Detection of Weld Defects by High Speed Imaging of the Vapor Plume
AbstractUsing two high speed cameras, we analyzed the 3D vapor plume fluctuations during laser welding of steel sheets in overlap configuration. Our results indicate that the position of the vapor plume contains relevant information on the process state. Whereas an increase of the penetration depth shifts the plume position in negative welding direction, welding defects like spatter formation or holes in the weld seam cause strong fluctuations of the plume position laterally transverse to the welding direction
E11 protein stabilisation by proteasome inhibition promotes osteocyte differentiation and may protect against osteoarthritis bone pathology
Supporting Accurate Interpretation of Self-Administered Medical Test Results for Mobile Health: Assessment of Design, Demographics, and Health Condition
Background: Technological advances in personal informatics allow people to track their own health in a variety of ways, representing a dramatic change in individualsâ control of their own wellness. However, research regarding patient interpretation of traditional medical tests highlights the risks in making complex medical data available to a general audience.
Objective: This study aimed to explore how people interpret medical test results, examined in the context of a mobile blood testing system developed to enable self-care and health management.
Methods: In a preliminary investigation and main study, we presented 27 and 303 adults, respectively, with hypothetical results from several blood tests via one of the several mobile interface designs: a number representing the raw measurement of the tested biomarker, natural language text indicating whether the biomarkerâs level was low or high, or a one-dimensional chart illustrating this level along a low-healthy axis. We measured respondentsâ correctness in evaluating these results and their confidence in their interpretations. Participants also told us about any follow-up actions they would take based on the result and how they envisioned, generally, using our proposed personal health system.
Results: We find that a majority of participants (242/328, 73.8%) were accurate in their interpretations of their diagnostic results. However, 135 of 328 participants (41.1%) expressed uncertainty and confusion about their ability to correctly interpret these results. We also find that demographics and interface design can impact interpretation accuracy, including false confidence, which we define as a respondent having above average confidence despite interpreting a result inaccurately. Specifically, participants who saw a natural language design were the least likely (421.47 times, P=.02) to exhibit false confidence, and women who saw a graph design were less likely (8.67 times, P=.04) to have false confidence. On the other hand, false confidence was more likely among participants who self-identified as Asian (25.30 times, P=.02), white (13.99 times, P=.01), and Hispanic (6.19 times, P=.04). Finally, with the natural language design, participants who were more educated were, for each one-unit increase in education level, more likely (3.06 times, P=.02) to have false confidence.
Conclusions: Our findings illustrate both promises and challenges of interpreting medical data outside of a clinical setting and suggest instances where personal informatics may be inappropriate. In surfacing these tensions, we outline concrete interface design strategies that are more sensitive to usersâ capabilities and conditions
The need for robust critique of arts and health research: Danceâmovement therapy, girls, and depression
We examine a highly cited randomized controlled trial on dance-movement therapy with adolescent girls with mild depression and examine its treatment in 14 evidence reviews and meta-analyses of dance research. We demonstrate substantial limitations in the trial which seriously undermine the conclusions reached regarding the effectiveness of dance movement therapy in reducing depression. We also show that the dance research reviews vary substantially in their treatment of the study. Some reviews provide a positive assessment of the study and take its findings at face value without critical commentary. Others are critical of the study, identifying significant limitations, but showing marked differences in Cochrane Risk of Bias assessments. Drawing on recent criticisms of systematic reviewing and meta-analysis, we consider how reviews can be so variable and discuss what is needed to improve the quality of primary studies, systematic reviews, and meta-analyses in the field of creative arts and health
pMel17 is recognised by monoclonal antibodies NKI-beteb, HMB-45 and HMB-50 and by anti-melanoma CTL.
Recently, we cloned the cDNA encoding the melanocyte lineage-specific antigen gp100 and demonstrated that gp100 is recognised by three different monoclonal antibodies (MAbs) used to diagnose malignant melanoma. In addition, we showed that tumour-infiltrating lymphocytes (TIL 1200) from a melanoma patient reacted specifically with cells transfected with the gp100 cDNA. Molecular characterisation of the gp100 cDNA revealed that the gp100 antigen is highly homologous, but not identical, to another melanocyte-specific protein, pMel17. Here, we report that cells transfected with pMel17 cDNA also react with all three MAbs used to diagnose malignant melanoma, NKI-beteb, HMB-45 and HMB-50. Moreover, pMel17 transfectants are specifically lysed by TIL1200. These data demonstrate that antigenic processing of both gp100 and pMel17 give rise to peptides seen by anti-melanoma cytotoxic T lymphocytes (CTL) and are therefore potential targets for immunotherapy of malignant melanoma
Ultrafast internal conversion and photochromism in gas-phase salicylideneaniline
Salicylidenaniline (SA) is an archetypal system for excited-state
intramolecular proton transfer (ESIPT) in non-planar systems. Multiple channels
for relaxation involving both the keto and enol forms have been proposed after
excitation to S with near-UV light. Here we present transient absorption
measurements of hot gas-phase SA, jet-cooled SA, and SA in Ar clusters using
cavity-enhanced transient absorption spectroscopy (CE-TAS). Assignment of the
spectra is aided by simulated TAS spectra, computed by applying time-dependent
complete active space configuration interaction (TD-CASCI) to structures drawn
from nonadiabatic molecular dynamics simulations. We find prompt ESIPT in all
conditions followed by the rapid parallel generation of the trans-keto
metastable photochrome state and fluorescent keto state in parallel. Increasing
the internal energy increases the photochrome yield and decreases the
fluorescent yield and fluorescent state lifetime observed in TAS. In Ar
clusters, internal conversion of SA is severely hindered but the photochrome
yield is unchanged. Taken together, these results are consistent with the
photochrome being produced via the vibrationally excited keto population after
ESIPT
Ultrafast internal conversion and photochromism in gas-phase salicylideneaniline
Salicylideneaniline (SA) is an archetypal system for excited-state intramolecular proton transfer (ESIPT) in non-planar systems. Multiple channels for relaxation involving both the keto and enol forms have been proposed after excitation to S1 with near-UV light. Here, we present transient absorption measurements of hot gas-phase SA, jet-cooled SA, and SA in Ar clusters using cavity-enhanced transient absorption spectroscopy (CE-TAS). Assignment of the spectra is aided by simulated TAS spectra, computed by applying time-dependent complete active space configuration interaction (TD-CASCI) to structures drawn from nonadiabatic molecular dynamics simulations. We find prompt ESIPT in all conditions followed by the rapid generation of the trans keto metastable photochrome state and fluorescent keto state in parallel. Increasing the internal energy increases the photochrome yield and decreases the fluorescent yield and fluorescent state lifetime observed in TAS. In Ar clusters, internal conversion of SA is severely hindered, but the photochrome yield is unchanged. Taken together, these results are consistent with the photochrome being produced via the vibrationally excited keto population after ESIPT
Improvement of the coupled-cluster singles and doubles method via scaling same- and opposite-spin components of the double excitation correlation energy
© 2008 American Institute of Physics. The electronic version of this article is the complete one and can be found at: http://dx.doi.org/10.1063/1.2883974DOI: 10.1063/1.2883974There has been much interest in cost-free improvements to second-order Moller-Plesset perturbation theory (MP2) via scaling the same- and opposite-spin components of the correlation energy (spin-component scaled MP2). By scaling the same- and opposite-spin components of the double excitation correlation energy from the coupled-cluster of single and double excitations (CCSD) method, similar improvements can be achieved. Optimized for a set of 48 reaction energies, scaling factors were determined to be 1.13 and 1.27 for the same- and opposite-spin components, respectively. Preliminary results suggest that the spin-component scaled CCSD (SCS-CCSD) method will outperform all MP2 type methods considered for describing intermolecular interactions. Potential energy curves computed with the SCS-CCSD method for the sandwich benzene dimer and methane dimer reproduce the benchmark CCSD(T) potential curves with errors of only a few hundredths of 1 kcal molâ»Âč for the minima. The performance of the SCS-CCSD method suggests that it is a reliable, lower cost alternative to the CCSD(T) method
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