ライフサイエンスコーパス: simulate

1 s ranging from milliseconds to one hour were simulated.

2 nding to 3,221 experimental data points were simulated.

3 iency of 1.5% with stability over 10 h under simulated 1 sun conditions employing a broad range of so

4 in the critical frequency by blocking I (h) Simulating 1000 synchronized layer 5 PCs, we reproduced

5 ed by using the LoTToR on a phantom, i.e., a simulated 3D reconstruction from a low-tilt series of im

6 n strontium-88 atoms in an optical cavity to simulate a collective Lipkin-Meshkov-Glick model(25,26),

7 We simulated a range of different nonpharmaceutical interve

8 To test this assumption, we simulated a reinforcement learning (RL) agent equipped w

9 To address this issue, we simulated a systemic virus exposure in early pregnant ra

10 We also simulated a two-dimensional spatial version of this mode

11 t was instructed not to speak for 2 minutes, simulating a "no-talking" policy, while in an ophthalmic

12 ated with chronic intermittent hypoxia (CIH) simulating a severe condition of obstructive sleep apnea

13 en repeated while reading a 2-minute script, simulating a talking patient.

14 ics of active networks [MEDYAN]); this model simulates actomyosin network dynamics as a result of che

15 to 70 dB sound pressure level at 9 kHz were simulated, advection speed was as large as 1 mm/s in the

16 Simulated aggregation levels at the group and individual

17 We observe that computer-simulated aggregation levels mimic true disease patterns

18 ents data from 2011 to 2016 toward the Liver Simulated Allocation Model to compare outcomes by age an

19 "junior residents") were asked to perform a simulated ALND.

20 al mechanical perturbations, was utilised to simulate and examine modulation of the activation dynami

21 nsemble, enetLTS, Rlogreg) were compared for simulated and an RNA-seq dataset.

22 We compared results from simulated and clinical infections with data from known r

23 Using both simulated and experimental data, we demonstrate that the

24 Using both simulated and experimental data, we show that this model

25 We consider a broad array of simulated and experimental datasets to demonstrate the e

26 he segmentation accuracy of BCM3D using both simulated and experimental images.

27 Simulated and experimental results show that a lens with

28 Using simulated and experimental RNA-sequencing data sets, we

29 erforms four state-of-the-art TAD callers in simulated and experimental settings.

30 First, we benchmarked metaFlye using simulated and mock bacterial communities and show that i

31 e showcase the analysis of two datasets, one simulated and one from a breast cancer patient, and over

32 00-fold acceleration in computation for both simulated and patient data.

33 We use vg to align simulated and real aDNA samples to a variation graph con

34 aGrid, to detect outlier samples in multiple simulated and real biological RNA-seq data sets with pos

35 presents experimental results obtained using simulated and real chemical datasets.

36 We demonstrate, using both simulated and real data that using these classes results

37 at HiNT outperforms existing methods on both simulated and real data.

38 We test our method on a combination of simulated and real datasets under various setups.

39 gorithm also runs efficiently when tested on simulated and real human genomic data, and thus can be p

40 of both worlds by building a mapping between simulated and real metabolic data through a novel method

41 is question, we perform benchmark studies on simulated and real scRNA-seq data.

42 e the performance of SCATS, we analyzed both simulated and real scRNA-seq datasets and compared with

43 Comparisons with existing approaches using simulated and real WGBS data show that our method provid

44 In a simulated anisometropic case, where the refraction power

45 ividual-based mathematical model was used to simulate annual HIV incidence among MSM cohorts.

46 sac of pregnant rats at Embryonic Day 20 to simulate antenatal models of chorioamnionitis and preecl

47 intervention in South Africa over 20 years, simulating approximately 175 000 individuals per run.

48 cal agar embedded with pencil lead fragments simulating as FBs.

49 ata include experiments from the literature, simulated assays, and primary MPRA data.

50 and environmental data on air monitoring and simulated atmospheric chemistry, we used a spatiotempora

51 In normal-hearing subjects listening to CI simulated audio, we showed that participants were able t

52 enhanced by addition of a reducing agent, to simulate availability of reducible substrates in vivo).

53 were inserted into a computational model to simulate axonal conduction, a rapid decrease in velocity

54 nal neural networks (CNNs) are trained using simulated biofilm images with experimentally realistic S

55 An individual-based model was developed, simulating births, deaths, HIV disease and treatment, af

56 d using 3 different sets of training images: simulated bone scan images, images of a cylindric phanto

57 simulated images of a cylindric phantom and simulated bone scan images.

58 ing when future outcomes have to be mentally simulated, but not when direct experience with stimulus-

59 l warming (+4 degrees C), sea level changes (simulated by altering of the inundation duration to 0, 2

60 ng experiments in which biodiversity loss is simulated by randomly assembling communities of varying

61 We test the ability of a vegetation model to simulate C cycling and community composition during 100

62 model of the HIV epidemic in South Africa to simulate CAB LA uptake by population groups with differe

63 Results from our experiments simulating captive aquaculture conditions demonstrated t

64 eal and adjust for population structure in a simulated case-control admixed population.

65 Innovations in algorithms to reconstruct and simulate cellular length scale phenomena based on emergi

66 tier for in silico biology is the ability to simulate cellular processes using these observed geometr

67 d from urethral swabs and in the presence of simulated Chlamydia coinfection.

68 lations outperformed local populations under simulated climate change (snow removal) across all five

69 ng data that were labeled automatically from simulated clinical image interpretation.(C) RSNA, 2020.

70 ase describing the lesion into a microphone, simulating clinical interpretation.

71 We found that simulated closed-loop performance was robust to mismatch

72 f these materials, a rigorous bridge between simulated coarse-grained structures and spectroscopy has

73 ble emulsions were subjected to digestion in simulated conditions using in vitro gastrointestinal mod

74 ncluded aaRS recharging, Gln4p depletion was simulated, confirming slowed translation.

75 ial and freshwater species in the Amazon and simulated conservation for species from both realms.

76 uses an atomizer and fluorescent markers to simulate contamination of uncovered skin and hair of hea

77 The simulated cooling mode is determined by changes in the s

78 performs better than all other estimators in simulated correlation analyses.

79 This enables users to simulate cryo-electron tomogram images with non-deformab

80 nes and macromolecules together, to obtain a simulated cryo-electron tomogram image with deformable s

81 Since the content of the simulated cryo-ET is more complex and crowded compared w

82 ally assigned breaks intentionally placed in simulated data (i.e., true breaks) with weights averagin

83 col to eliminate sequencing errors from both simulated data and the raw reads.

84 oad >1000 copies/mL (treatment failure), and simulated data for 10 000 individuals over 5 years to co

85 We show that on simulated data POLCA is more accurate than Pilon, and co

86 Validation on real and simulated data sets shows that MPL is fast and accurate,

87 Analysis of real and simulated data shows that our method can identify large

88 We present examples using empirical and simulated data to demonstrate the performance of the pac

89 nal methods for gene expression analysis use simulated data to evaluate the accuracy of these methods

90 The experimental and simulated data were analyzed with hierarchical clusterin

91 CND improves phylogenetic reconstruction on simulated data where CNAs occur with varying probabiliti

92 We use simulated data with main effects, correlation and intera

93 We evaluate computational performance using simulated data, and show that calculating statistics fro

94 opes (SMLMs) are routinely benchmarked using simulated data, calibration rulers, or comparisons to se

95 Using simulated data, we show a high precision of 97% and a re

96 ed when assessment is focused too heavily on simulated data, where the alignment task is often simple

97 s with a competitive accuracy (> 0.86 on the simulated dataset with SNR = 0.1), or even one sample wi

98 We evaluate the method on simulated datasets and on real datasets from droplet-bas

99 We applied our framework to simulated datasets and to a real-world dataset.

100 The averages of the Jaccard index for the simulated datasets containing 2000 records were 0.705, 0

101 However, the simulated datasets may not reflect the real complexities

102 with SV information, we tested Meltos on two simulated datasets with five genomes in both.

103 On simulated datasets, DuploMap increased the percentage of

104 t none of the methods performed well for all simulated datasets.

105 dence that a large fraction (~29-53%) of the simulated decadal-scale variance in individual timeserie

106 We simulated dialytic removal of (1) phenytoin, initial con

107 on at temperatures as low as ~160 (o)C under simulated diesel exhaust conditions while using 5 times

108 a compartment model of the United States to simulate different influenza seasons and the impact of r

109 Frames were added to simulate different levels of administered activity.

110 framework that uses daily travel networks to simulate different outbreak and intervention scenarios a

111 , designed to provide a unified framework to simulate different types of data from healthy participan

112 We used a biophysical model to simulate different vocal fold oscillations, extended the

113 The effects of boiling and in vitro human simulated digestion on phenolic compounds and bioactivit

114 This multicompartment, flow-through system simulates digestion by transferring gastrointestinal flu

115 The simulated distribution was used to estimate the null dis

116 based and HSMRF-based models on a variety of simulated diversification scenarios, and then apply them

117 egimes of effectiveness within the different simulated dosage options.

118 Simulated dose in representative models is validated thr

119 within the Rosetta software suite capable of simulating double electron-electron resonance spectrosco

120 which is necessary to maintain canopy during simulated dry seasons.

121 alyze butterfly wings across a wide range of simulated environmental conditions, and find that region

122 We simulated environmentally realistic exposure of red-legg

123 ves for HMDSO, OMTSO and PDMSO was small and simulated errors in pO(2) measurement were 1-2 torr/ deg

124 l the main types of exine structure could be simulated experimentally.

125 By simulating experimentally the extinction of three consum

126 Many docking software packages can simulate flexible ligand docking, and among them, Autodo

127 in a community and this basis can be used to simulate forward by solving a relatively inexpensive sys

128 Here, we apply a new model to simulate future numbers of alien species based on estima

129 We simulate future trajectories of both RSV and influenza,

130 Both proteins were rapidly digested in simulated gastric fluid and their enzymatic activity was

131 d C. difficile inoculum, and pre-exposure to simulated gastric intestinal fluid (SGF) and simulated i

132 sess their bioaccessibility with an in vitro simulated gastrointestinal digestion according to the IN

133 li, pepper, spinach, kale and rocket after a simulated gastrointestinal digestion using a newly optim

134 P, are susceptible to degradation during the simulated gastrointestinal digestion.

135 ion and benefit the biogeochemical models in simulating global nitrogen cycling.

136 n Alaska, incubated them for 5 months with a simulated, gradual or abrupt temperature increase of +5

137 hyde (GA), and further calcified in vitro to simulate graft calcifications upon implantation was char

138 of As(III) could be selectively removed from simulated groundwater over 10 cycles at an ultralow ener

139 A comprehensive meta-analysis of simulated GWAS data has been incorporated demonstrating

140 Simulated GWAS datasets are also packaged with the pipel

141 dy the effect of residual stratification, we simulated GWAS under realistic models of demographic his

142 ketamine does not compromise tolerance to a simulated haemorrhagic insult.

143 By 2100, simulated Hg concentrations in the Yukon River increase

144 We used a Markov Model to simulate HIV and TB coinfected patient care in LMICs usi

145 We also simulate how either rapidly increased fish demand (drive

146 Finally, we used a mathematical model to simulate HRV under decreased "coupled-clock" regulation.

147 sms responsible for such variability through simulating human exposure via multiple exposure pathways

148 The simulated images could be regarded as the labeled data w

149 erimental images of C(18) were compared with simulated images for four theoretical model geometries,

150 The CNNs were evaluated with simulated images of a cylindric phantom and simulated bo

151 The simulated impact on near-surface climate properties at b

152 resence of an immune system are difficult to simulate in vitro.

153 Finally, the cascading invulnerability is simulated in several typical network models and the US p

154 ibed in the mouse, and therefore they can be simulated in sufficient detail to capture their intrinsi

155 These two possibilities were simulated in the different microwells with varied depth

156 ng currents measured in NMR spectroscopy and simulated in time-dependent density functional theory ca

157 By analyzing and simulating inactive conformations of the highly homologo

158 6-9 and carbonate-buffered) was developed to simulate incomplete bromide (Br(-)) oxidation during sho

159 comes model, a Markov state transition model simulating individuals' long-term outcomes, healthcare c

160 In simulated infections, if >=10(4) CFU/ml of N. gonorrhoea

161 From the simulated infections, we estimated hospitalizations, dea

162 al resolution of ESMs and their inability to simulate intense and short rainfall events mask effects

163 r and to reduce the required sample size for simulated interventional trials.

164 ron sized particles have been compared under simulated intestinal conditions.

165 atments, a higher affinity for bacteria than simulated intestinal epithelium, a valuable activity at

166 simulated gastric intestinal fluid (SGF) and simulated intestinal fluid (SIF), on the antibacterial a

167 , 1.6, and 2 mmol/mL) and by positioning the simulated intravenous line within several fields of view

168 le-to-male grooming strength decreased after simulated intrusions compared to female-to-female groomi

169 Simulated ion trajectories were used to rationalize the

170 endorff heart preparations before and during simulated ischemia.

171 mplitude relatively well, the majority still simulates its asymmetry between warm (El Nino) and cold

172 days, and concentrations were compared with simulated kinetic profiles.

173 izontal ocean currents, vertical swimming of simulated larvae can have an order of magnitude impact o

174 In a simulated laundering experiment, the EMEL concentrations

175 From each of the simulated lesions, 25 radiomics features related to the

176 ion efficiency of 4.33% under AM 1.5 G solar simulated light.

177 Effects of DIO were recapitulated by simulating lipotoxicity in skeletal muscle cells treated

178 Specifically, we found that the simulated mechanism of action of RUTI and INH are in goo

179 mechanical and agent-based model (Mech-ABM), simulating mechanotransduction in a single osteoblast un

180 Stimulation of the terminals in simulated models of inflammatory or neuropathic hyperexc

181 To simulate MS and HB, an existing computational model of p

182 C, we developed clusterlab, a new method for simulating multivariate Gaussian clusters.

183 ary, we found that the divergent response to simulated N deposition depended on ambient N deposition

184 er maximum photosynthetic capacity maximised simulated NCE under aseasonal high mean LAI, with the re

185 mbles in prefrontal cortex, hippocampus, and simulated neural networks simultaneously represented mul

186 trap iterations in different subsets of data simulating new incoming data in 6-month batches.

187 Simulated night shifts were used to induce a misalignmen

188 Besides, simulating non-deformable and deformable components unde

189 active vertex model to experiments, we have simulated numerically a confluent cellular monolayer spr

190 s in each country to assess their ability to simulate observed yield.

191 olved advection) on patterns of observed and simulated ocean warming remains a challenge.

192 ittency is reliably detectable when sampling simulated odorants on the order of seconds, and provides

193 er, the existing methods are based on either simulated or limited experimental datasets.

194 However, there is a lack of tools to simulate pangenome variability and structure using defin

195 ypothesis with more than [Formula: see text] simulated particles with a range of active swimming beha

196 mpassing drug resistance and radiobiology to simulate patterns of local versus distant recurrences in

197 Simulated patterns of involvement across cortical areas

198 vailability was determined using an in vitro simulated peptic-pancreatic digestion, followed by measu

199 We design a simulated perturbation process to characterize the contr

200 ped simplePHENOTYPES, an R/CRAN package that simulates pleiotropy, partial pleiotropy, and spurious p

201 estation and then withdrawn from estrogen to simulate postpartum estrogen withdrawal.

202 Simulated practice, both face-to-face and computer-based

203 Finally, CLZ depth injection simulated preferential flow and demonstrated the importa

204 Additionally, we experimentally simulated previously reported ETV/3TC resistance for HBV

205 d on moire superlattices that can be used to simulate problems in strong-correlation physics that are

206 DO fluxes at the SWI calculated from the simulated profiles with the negative-flux lower boundary

207 reement with the observed DO fluxes than the simulated profiles with the zero-flux lower boundary con

208 We simulate prostate-specific antigen (PSA) dynamics, with

209 ctural data, developing a novel algorithm to simulate protein complex dynamics.

210 ich culminated in IL-1beta induction thereby simulating pseudohypoxia.

211 ped to elucidate the reaction mechanisms and simulate reaction kinetics of UV/PAA process.

212 Simulated real-world studies are conducted in consecutiv

213 Here I present efficient software for simulating reconstructed phylogenies under time-dependen

214 Simulated reconstructions, using linear-nonlinear cascad

215 xtracellular recordings and state-of-the-art simulated recordings.

216 l predictions of NPP; (4) to test effects of simulated reductions of phytoplankton biomass or nutrien

217 ngstanding uncertainties in their ability to simulate regional and local precipitation extremes and r

218 Our simulated results compare favorably with recent experime

219 The simulated results showed that the model was capable of p

220 Using both simulated Ribo-seq footprint data and three benchmark da

221 Among 173 simulated ridges, 115 can be tracked (RMSD < 0.001).

222 or showed almost the same sensitivity in the simulated river water samples as in phosphate buffer, re

223 ducing positive affective states is by human-simulated rough and tumble play or 'tickling' [3,4].

224 r transportation of laboratory samples under simulated routine conditions and public health emergency

225 arge-scale rubber cultivation is viable, and simulated rubber expansion under different scenarios.

226 rmance of these methods on a wide variety of simulated samples, as well as two real data samples.

227 en provide two vignettes illustrating how to simulate sets of correlated traits in simplePHENOTYPES.

228 misalignment underpins mood vulnerability in simulated shift work.

229 cal samples under various storage conditions simulating shipping in hot or cold climates.

230 ) acquired from parents while they shop in a simulated shopping market as well as follow up functiona

231 where a system of connected rivers is to be simulated simultaneously.

232 For the in silico study, we simulate single cells from TF/pathway perturbation bulk

233 We develop a strategy to simulate single-cell transcriptional data from synthetic

234 gnostic performance of dual-energy CT versus simulated single-energy CT in the differentiation of sma

235 smission heterogeneity under a wide range of simulated situations, including incomplete sampling, var

236 Simulating sleep after new learning reversed the damage

237 operties due to hindlimb unloading alone and simulated spaceflight.

238 implifications of complex systems, and often simulate specific processes at single scales (e.g. tempo

239 FORCCHN2 simulates spring and autumn phenological events from hea

240 The model is simulated stochastically by sampling the parameter value

241 controlled-release proton pump inhibitors in simulated stomach and intestinal contents, as well as co

242 ratios over the Arabian Gulf are adequately simulated, strong underprediction by the model was found

243 dth (TRW) records, growing season length and simulated subdaily soil hydrology to parameterize ring w

244 We modify an ocean model to simulate submarine iceberg melting in Sermilik Fjord, ea

245 Further, comparison of simulated sunlight inactivation efficacy in maturation p

246 rom different plants, 36 h of irradiation by simulated sunlight removed 28-33% of DCAN-FP and 41-48%

247 d decay rates were dependent on the level of simulated sunlight, but they were not significantly diff

248 This study examined effect of simulated sunlight, relative humidity, and suspension ma

249 However, at full intensity simulated sunlight, the mean decay constant was 0.29 +/-

250 At such extremes of simulated system complexity, the largest stable complex

251 ect quadrature method of moments (ADQMOM) to simulate the abrupt-rise process of haze development and

252 MBITES, it is possible to build models that simulate the behavior and ecology of adult mosquitoes in

253 large scales, first, tree-level models that simulate the carbon costs of drought-induced plant hydra

254 to a broad range of disciplines: models that simulate the geometries and mechanical properties of sof

255 n cyclical work loop experiments designed to simulate the in vivo dynamics of muscle fibers during sw

256 To more closely simulate the low-dose rates found in space, sequential f

257 hardware configurations that can be used to simulate the network on specialized cytomorphic hardware

258 hanistic model to climate reconstructions to simulate the past 50,000 years of bird migration worldwi

259 dimensional (3D) computational framework to simulate the performance and response of deeply implante

260 we use a climate-dependent epidemic model to simulate the SARS-CoV-2 pandemic by probing different sc

261 ation model tied to a fire behavior model to simulate the spread of buffelgrass (Cenchrus ciliaris) i

262 A half-space dislocation model is used to simulate the theoretical values of the postseismic displ

263 We simulate the urban climate of various generated cities u

264 composed of four sub-models is developed to simulate the urbanization and energy consumption in Chin

265 known whether influenza vaccine is leaky, we simulated the 2011-2012 to 2014-2015 influenza seasons t

266 We simulated the allocation of kidneys from 2200 deceased d

267 We simulated the diaphragm's in vivo cyclical length change

268 e-selectivity of REMPI in ion traps, we have simulated the expected broadening of the ionisation thre

269 We simulated the Mg-doped GaN transport properties by densi

270 We simulated the proposed neural mechanisms and tested mode

271 model of AMPA receptor phosphorylation that simulates the induction of long-term depression (LTD) an

272 ere, we present an in vitro human model that simulates the initial apical infection of alveolar epith

273 We propose an experimental setup that simulates the intracranial hydrodynamics of a pneumoceph

274 developed an in vivo compression device that simulates the solid mechanical forces exerted by a growi

275 pportunities to Egypt, Sudan and Ethiopia by simulating the filling period of the reservoir; a new no

276 A variety of microstructures, simulating the full range of exine types, was obtained b

277 We confirmed our results by simulating the impact of specific peptide mutations and

278 imulator, a powerful tool that is capable of simulating the mutational landscapes of thousands of can

279 We simulated these mutations in both GDP- and GTP-bound Cdc

280 Here, we develop a computational model to simulate this chain of olfactory processing from the rec

281 time, the time to re-extend tentacles after simulated tidal immersion.

282 pid-protein interaction profile of all GPCRs simulated to facilitate analysis and comparison of our d

283 presenting realistic recording schemes) were simulated to validate SIRE and to assess their impact on

284 additional chemicals of interest, as well as simulated ToxCast(TM) metabolites, totaling 55,450 chemi

285 de in conjunction with our dynamic model, we simulate transmission dynamics of seasonal influenza in

286 gnificantly improves the spatial patterns of simulated tree cover, which demonstrates the need to rep

287 effectiveness of our pedigree approach on a simulated trio of pseudo-diploid yeast genomes with diff

288 In addition to simulated tumors with varying number of biopsies, we dem

289 % for two of the three sealant fluids during simulated urination to a urinal cartridge but removal of

290 to the nearest region with unused beds were simulated using an algorithm that minimized total inter-

291 tion in response to climate change have been simulated using both statistical and process-based model

292 using single-edge precracked beam method and simulated using reactive molecular dynamics.

293 ; this surprising result is confirmed by DFT-simulated UV-vis spectra.

294 dose, to 85% body surface area, using solar simulated UVR or narrowband UVB (311 nm).

295 icipants experienced a variable magnitude of simulated VF loss based on longitudinal data from a real

296 were not capable of consistently identifying simulated VF loss, despite it being of a magnitude likel

297 We used a gaze-contingent simulated visual field (VF) loss paradigm, in which part

298 We constructed simulated wild turkey nests throughout the home ranges o

299 educed incidence of reproductive dormancy in simulated winter conditions, while flies overexpressing

300 The procedures were simulated with finite element analysis.