ライフサイエンスコーパス: plot

1 reference tissue model 2 and Logan reference plot.

2 on (EBSD) orientation density function (ODF) plot.

3 nd 3-tissue-compartment models and the Logan plot.

4 chieved from the linear range of calibration plot.

5 eratures were significantly higher in warmed plots.

6 s higher in fertilized compared with control plots.

7 correlated with the geographical distance of plots.

8 otR, a Perl/R pipeline for creating metagene plots.

9 ecreased by 28% in the high burning severity plots.

10 y influential studies using Amazonian forest plots.

11 ce for 63 vascular plant species across 5170 plots.

12 ies in a regional network of forest dynamics plots.

13 be derived from pretest-posttest probability plots.

14 ased on observations at >40 000 field survey plots.

15 re statistically compared using Bland-Altman plots.

16 s of sgRNAs and genes, and publication-ready plots.

17 rich set of QC metrics and publication-ready plots.

18 excluded relevant sources of bias by funnel plots.

19 analytical detection of asymmetry in funnel plots.

20 n's correlation coefficient and Bland-Altman plots.

21 case definition, and GA-specific probability plots.

22 in 15 replicate plots paired with 15 control plots.

23 reduction of total biomass in high diversity plots.

24 uent flood years by 15% compared to control plots.

25 the 24 hr mean of Rs, especially in trenched plots.

26 on correlation coefficients and Bland-Altman plots.

27 characteristic (ROC) curves, and calibration plots.

28 espiration, was greater in soils from warmed plots.

29 information criterion, F test, and residual plots.

30 3 age groups, and agreement in rankings was plotted.

31 Viral load density distributions were plotted.

32 r operating characteristic (ROC) curves were plotted.

33 g chromosome-aware interval queries and read plotting.

34 seaweed Gracilaria vermiculophylla in large plots (25 m(2)) on southeastern US intertidal landscapes

35 mblages of angiosperm trees in 0.1-ha forest plots across China to examine the effects of environment

36 Using a network of plots across five mountain ranges, we described patterns

37 f more permanent carbon intensive monitoring plots across the tropics.

38 As a result, the rate of ATP synthesis, plotted against [ADP], remains low until [ADP] reaches a

39 nts (52%), correct vascular procedural steps plotted against anatomy knowledge (the 2 IPS components

40 sIgG and sIgE titers plotted against exposure duration were compared between

41 n the region of interest for each tumor were plotted against MR ADC values.

42 ence in cores analyzed in 1994 and 2014 when plotted against sediment (radiometric) age, indicating t

43 ts of the Standardized Mean Difference (SMD) plotted against the standard error (SE) are susceptible

44 Model simulations of heated plots agreed with our observations and predicted loss of

45 The calibration plot allowed a range of linearity extending between 15 a

46 g the autotrophic carbon budget in 16 forest plots along a 3300 m elevation transect in Peru.

47 ntory data from the USA and Mexico (>125,000 plots) along with climate data to address two questions:

48 reement was obtained for the Logan reference plot also for a reduced scan time of 100 min (R(2) = 0.9

49 at are relatively oversampled with inventory plots also contain the highest values of predicted ancie

50 Cartesian plot analysis revealed that M10(Full)LZ meandered on fil

51 Parametric images were generated using Logan plot analysis, a basis function method, and spectral ana

52 ht, ear length, ear weight/plot, grain yield/plot and 100 grain weight were enhanced in NPs treatment

53 nevin and colleagues now elegantly twist the plot and achieve ultimate selectivity: They target MMP-9

54 ed Mx, it showed its ability to detect inter-plot and inter-season differences on both growing sites.

55 The funnel plot and the Egger's test (p=0.44) showed no evidence of

56 detected recombination events by similarity plots and (v) annotation of genomic regions.

57 Bland-Altman plots and 95% limits of agreement (LoA) were used to eva

58 arget analysis utilized Kendrick mass defect plots and a "nontarget" R script.

59 as well as utilize long-term WPND monitoring plots and data collected from land-based weather station

60 idimensional graphical display featuring two plots and four axes, Guide Picker can analyze all guides

61 Soil porosity was higher in higher-diversity plots and had a positive effect on plant performance.

62 Quantile-quantile (QQ) plots and Manhattan plots are classical tools which have

63 water addition, water reduction and control plots and measured effects on vegetative and floral trai

64 ultiple dimensions, we created n-dimensional plots and metrics to characterize any set of quantitativ

65 d VA data using best fit on Lineweaver-Burke plots and modelled with non-linear regression using reci

66 bed using cumulative-hazard and Kaplan-Meier plots and multivariable analyses by Flexible Parametric

67 ), and synthesised graphically using harvest plots and narratively.

68 Renewed focus on large (1-50 ha) permanent plots and on spatial patterns of tree-layer variability

69 hr campaigns using two treatments: trenched plots and plots with shrubs.

70 iated with bare (unvegetated) patches in all plots and seasons.

71 features are facilitated through diagnostic plots and summary statistics computed over regions of th

72 l discrimination was measured by calibration plots and the concordance index.

73 parison, visualized in the browser as circle plots and topology diagrams.

74 by 25.2% in comparison with no-N deposition plots and turned the mesocosms from N2 O sinks to N2 O s

75 stribution volume (VND) via Lassen occupancy plotting and thereby estimate BPND in brain.

76 , 3D dispensing, 3D fiber deposition, and 3D plotting), and 3D bioprinting.

77 analysis, regression analysis, Bland-Altman plot, and paired sample t-tests were used to analyze the

78 Using a combination of treatment and control plots, and cages to exclude vertebrates, we made food re

79 Our analyses reveal that forest inventory plots, and especially forest recensus plots, in all regi

80 emical impedance spectroscopy, Mott-Schottky plots, and intensity-modulated photocurrent spectroscopy

81 hics, including univariate scatterplots, box plots, and violin plots, for comparing values of a conti

82 re using band shift assays, fluorescence Job plots, and yeast three-hybrid assays, we investigate the

83 duced lower yields than conventional in both plot- and field-scale experiments.

84 ackage to flexibly and quickly summarize and plot annotations of genomic regions.

85 The resulting action plots are assessed in the context of Beer-Lambert's law

86 Quantile-quantile (QQ) plots and Manhattan plots are classical tools which have been utilized to vi

87 Iron-binding speciation plots are consistent with ELT donating iron to deferasir

88 lished plots located along a tidal creek; 10 plots are on forest islands surrounded by salt marsh, an

89 to 0.4) when using precise field measures of plot area and when using larger fields for which roundin

90 shift in the distribution of spine densities plotted as a cumulative distribution, opposite to the ef

91 ion cross sections (CCS) were calculated and plotted as a function of mass-to-charge ratio.

92 Importantly, when plotted as function of sample size, the raw moments of t

93 When plotted as gender-dependent trends over time, all four c

94 Funnel plot asymmetry among SLC6A3 studies was identified and a

95 mple size and intervention effects on funnel plot asymmetry, using empirical datasets and illustrativ

96 Diversity-carbon relationships among all plots at 1 ha scale across the tropics are absent, and w

97 imentally warmed and nonwarmed common garden plots at Alexandra Fiord, Ellesmere Island in the Canadi

98 bient and +3.4 degrees C air and soil warmed plots at two sites in northern Minnesota.

99 PCA score plot based on both HPLC and UV spectroscopy showed the s

100 NEE also increased in Control (i.e., ambient plots), but this change could be explained by slow thaw

101 lower in elevated CO2 plots than in ambient plots, but did not differ between heat treatments.

102 tism on B. dracunculifoliae in the treatment plots, but did not significantly alter either the specie

103 frared heaters raised temperatures in heated plots, but raised temperatures more in the forest than a

104 n forest communities as measured in complete plot censuses, and on overall estimates of seed plant di

105 is introduced for extraction of current-time plots (chronoamperograms) from experimental potential-ti

106 mperograms) from experimental potential-time plots (chronopotentiograms).

107 arance of a characteristic maximum in the PL plot collected over time.

108 position of labile SOC was similar in warmed plots compared to the control.

109 comparison of the etch pit image and the ODF plot compellingly connects the macroscopic etch pit hexa

110 NICS calculations and ACID plots confirmed the diatropic nature of these structures

111 Ragone plot confirms that this device can make a synergetic bal

112 egression, heterogeneity testing, and forest plot construction.

113 Based on coordination charge and 3D XANES plots containing a series of model compounds as well as

114 The search of "volcano plots" correlating catalysis kinetics to the stability o

115 differential expression analysis, profiling plotting, correlation analysis, patient survival analysi

116 tude, by exploring relationships between per-plot counts of each life stage and the covariates hypoth

117 he expression stability was evaluated by box-plot, Cq analysis, NormFinder and BestKeeper statistical

118 ss the quantifiable range, with Bland-Altman plot data showing a mean difference (+/-1.96 standard de

119 ontrol plots, Rs in the low burning severity plots decreased by 19%, while it decreased by 28% in the

120 discussed in a three-dimensional calibration plot demonstrating the sensor's suitability to enable a

121 ach of those panels contains a series of X-Y plots depicting expression levels of subsystems of that

122 representations of the hairpin structure and plots depicting the alignment of sequences on the second

123 s exhibited discontinuities in the Arrhenius plots, distinguishing the unfolding and aggregation phas

124 We used SAS survey procedures to plot distributions of TBI and produce prevalence estimat

125 ng a significant decline in the diversity of plots driven by increasingly severe postfire summer weat

126 prediction rate of 0.843 area under the ROC plot due to the change in magnitude of the electrostatic

127 warmed (14.5%) compared with control (13.5%) plots during the growing season even though surface soil

128 kg) between adjacent replacement and control plots during two boro seasons.

129 ture-mark-recapture surveys of rodents on 30 plots each year.

130 The fitted calibration plots exhibit larger coverage with less data scattering

131 We find that frequently burned plots experienced a decline in surface soil carbon and n

132 Sixteen plot experiments and ten on-farm experiments were conduc

133 Compared to control plots, food webs in manipulated plots had significantly

134 An Eyring plot for beta-hydride elimination-olefin rotation-reinse

135 The theoretically predicted volcano plot for hydrogen production shows the best catalyst as

136 It uses cumulative probability (CP) plots for spatially representative data sets, preferably

137 g the slopes of charge density versus Deltaf plots for the Ag electrodeposition.

138 ivariate scatterplots, box plots, and violin plots, for comparing values of a continuous variable acr

139 Featured functions, such as sequence plot, fragment segmentation, measure tool and meta-infor

140 Plots from Logan and MA1 graphical methods became linear

141 Finally, an extremely flexible plotting function enables quantitative representation of

142 rtition probabilities and diagnostic density plots further allow for some quality control.

143 The comparison of Ragone plots further discloses that NVPF-NTP presents the best

144 g of those syntenic datasets to identify and plot gene retention patterns.

145 riment, plant height, ear length, ear weight/plot, grain yield/plot and 100 grain weight were enhance

146 Although Avicennia plots had more elevation capital, suggesting longer surv

147 d to control plots, food webs in manipulated plots had significantly lower values of weighted connect

148 notic EID risk index, and partial dependence plots illustrating relationships between events and pred

149 experiment, we suppressed ants from c. 1 ha plots in a lowland tropical rainforest in Sabah, Malaysi

150 utive years of data from tropical rainforest plots in Costa Rica that range from 10 y since abandonme

151 ata for >34 000 trees from several permanent plots in French Guiana to investigate if soil characteri

152 by the flood when grown in higher-diversity plots in July 2013.

153 longest running set of permanent vegetation plots in the Fynbos of South Africa (44 y), finding a si

154 on larger trees between burned and unburned plots in the long term.

155 ia, in both seagrass and unvegetated control plots in the low intertidal and shallow subtidal zone.

156 We established experimental maize plots in western Kenya to allow us to quantify the respo

157 entory plots, and especially forest recensus plots, in all regions of Amazonia are located disproport

158 Van Deemter plots indicated higher efficiencies for the 3D serpentin

159 Lineweaver-Burk plots indicated that 5-CQA exerts a mixed type inhibitio

160 he AAScatterPlot tool compacts into a single plot, information about the hydropathy index, Van der Wa

161 ssed via Begg's and Egger's tests and funnel plot inspection.Findings from 12 RCTs (n = 609 participa

162 The Extended Inhibition Plot introduced here yielded an estimate of the volume o

163 f-level field measurements and species-level plot inventory data and find reasonable agreement.

164 rrect, a portion of the sigmoid on a log-log plot is very close to linear, allowing the unknown endog

165 From the gradient of the calibration plot, limit of detection (LOD), and sensitivity were cal

166 ory composition in 13 previously established plots located along a tidal creek; 10 plots are on fores

167 Its sampling design includes many plots located in humid ecosystems and ignores critical a

168 compile a unique pan-tropical dataset of 360 plots located in structurally intact old-growth closed-c

169 e examine whether Amazonian forest inventory plot locations are spatially biased toward areas with hi

170 cm of soil between 13 high-As and 13 low-As plots managed by 16 different farmers, and we explore th

171 By Bland-Altman plot, mean maximal LVWT difference between echocardiogra

172 s, LC-MS, FIR, Fluorescence titration, Job's plot method and theoretical approaches.

173 on previously established stable isotope bi-plot metrics.

174 osely match those from African and Amazonian plot networks, suggesting that the world's remaining int

175 lis became the predominant species, while in plots not treated with insecticides, T. tabaci remained

176 graphics functions are implemented to easily plot numerical or categorical data associated with the r

177 dimerization were determined from van't Hoff plots obtained from variable-temperature electron parama

178 However, the force plots obtained with serum-modified tips are very differe

179 hourglass magnetic dispersion and the Yamada plot of incommensurability versus doping in terms of the

180 CPET rate constants, and a combined Bronsted plot of ln(kMS-CPET) vs ln(Keq) was linear with a slope

181 n that is estimated by fitting a line to the plot of log bending energy against log variance explaine

182 The Arrhenius plot of the adsorption/desorption rate constants measure

183 A linear log-log plot of the distribution showed a more homogeneous distr

184 sity was significantly less than in adjacent plots of a less-common pasture grass (Lolium multiflorum

185 Data is presented from three neighboring plots of bauxite residue that was deposited 20 years ago

186 The plots of DeltaG(double dagger) vs approximated DeltarG d

187 of cell walls along the elongation zone, but plots of growth rate versus wall compliances were striki

188 manipulating, and graphing publication-ready plots of hierarchical data.

189 biturate anions were derived from the linear plots of log k2 versus the electrophilicity parameters E

190 aking with mechanical stirring), with linear plots of peak current vs cumulative concentration of TNT

191 n visual inspection of fractional polynomial plots of the association between ESI and indices of stra

192 Linearized plots of the percentages of (4)C1 against limiting JCH a

193 constants were obtained as the slopes of the plots of the pseudo-first-order rate constants versus th

194 We found that funnel plots of the Standardized Mean Difference (SMD) plotted

195 The data were plotted onto a world map representing eight major sampli

196 ulations by traditional gating using biaxial plots, or identification of populations that display sma

197 more hydrophilic environment, while concave plots originate from AOs in a more hydrophobic location

198 parameters, with linear Arrhenius and Eyring plots over an exceptionally wide temperature range of 11

199 tics of probability distributions: spaghetti plots over one dimensional projection, heatmaps of distr

200 c relatedness, body mass and the size of the plots over which densities were estimated.

201 ted with B. dracunculifolia, in 15 replicate plots paired with 15 control plots.

202 Overlaid contour plots prediction showed that the optimal conditions for

203 ominance was switched - ECM trees dominating plots previously occupied by AM trees, and vice versa -

204 that the percentage of AM or ECM trees in a plot promotes microbial communities that both reflect an

205 PCA plot proved the potential of reproducibility of analyses

206 Of the 2 graphical models tested, the Patlak plot provided adequate results for the tumor and brain,

207 The Logan plot provided the best estimate of tau binding using art

208 by plot-scale experiments (0.02-ha to 1.0-ha plots) provided a comparison of plot versus field perfor

209 same plane in a cell are used in the phasor plot providing a solution to analyze multiple lifetime o

210 ut significantly higher (13.0% vs. 11.0%) in plots receiving added winter rain relative to controls,

211 net isotope effect, but the proton inventory plot remains linear, consistent with an unchanging rate-

212 Plot representativeness of trait distributions at landsc

213 0.16 mm for cutting and 0.19 and 0.17 mm for plotting, respectively.

214 A Bayesian skyline plot revealed the rapid expansion of CRF01_AE in China a

215 The response plots revealed that addition of methanol noticeably impr

216 Compared with the control plots, Rs in the low burning severity plots decreased by

217 tal data from 95 white spruce (Picea glauca) plots sampled across a longitudinal gradient in southwes

218 For soybeans at the plot scale, biological and conventional managements prod

219 For all three crops, at the plot scale, reduced-input and conventional managements p

220 ng neighbouring trees varied, but not at the plot scale.

221 ly based on observations at the experimental plot scale.

222 Although yield gaps between plot-scale and field-scale research are widely acknowled

223 Nearby plot-scale experiments (0.02-ha to 1.0-ha plots) provide

224 We found that plot-scale yields well matched field-scale yields for co

225 known to regulate soil respiration rates at plot scales within certain biomes, quantitative framewor

226 In contrast, the Logan plot showed excellent fits and parameter variance (total

227 Compared to the control, soils from warmed plots showed significant increase in the signal intensit

228 Calibration plots showed the new risk score to have good calibration

229 Main effect plots showed total FAAs extraction was favoured under co

230 , we analyze data from three forest dynamics plots spanning a moisture gradient in Panama that have e

231 ce of markers with different types of paper, plotting speeds, and pattern dimensions.

232 oss three main forest types of PNG using 193 plots stratified across 3,100-m elevation gradient.

233 avorably with a global compilation of paired plot studies.

234 hetic rates by altering CO2 concentration in plots subjected to +200 ppmv for 15 years.

235 d this shift was accelerated in more diverse plots, suggesting that a large species pool is important

236 idimensional scaling and principal component plots, supported by an analysis of molecular variance, s

237 In calibration plots, survival distributions predicted by the nomogram

238 re dispersed among species in high-diversity plots than expected based on monocultures.

239 ll treatments and were lower in elevated CO2 plots than in ambient plots, but did not differ between

240 These effects occurred in plots that integrated different ecosystem types (i.e., m

241 ficantly, particularly in warmed, fertilized plots that received additional winter precipitation.

242 he spatial scale of seed mixing, doubling in plots that received seed from large (>/=5 km) compared w

243 We resampled plots that were established in 1972 and repeated the ful

244 per cent) less nitrogen after 64 years than plots that were protected from fire.

245 a or images requires more PCs than needed to plot the largest population shifts.

246 an online Javascript calculator that easily plots the expected serum PFOA concentration over time an

247 Using natural cubic splines, we plotted the hazard ratio for all-cause mortality and car

248 ctrochemical impedance spectroscopy (EIS) by plotting the peak current and Rct against PSA concentrat

249 Plotting the phasors allowed for decomposition, unmixing

250 mosphere, causing the planet to seem bigger; plotting the planet's observed size as a function of the

251 e measure as effect size (when possible), or plotting the SMD against a sample size-based precision e

252 urvature of the log(rate) versus temperature plot (the change in heat capacity for the system, DeltaC

253 When fitted into the HER volcano plot, the MoS2 active sites follow a trend distinct from

254 alyzing more than 210,000 0.5-hectare sample plots through a photo-interpretation approach using larg

255 We suggest a simple and familiar plot to assess heterogeneity across outcomes, which shou

256 We constructed forest plots to determine the sensitivity and specificity of de

257 d at 1, 3, 6, 12, 18, and 24 months and were plotted to observe their trend.

258 ts) with a forest inventory dataset (105,316 plots) to extrapolate and map relationships between vari

259 Here we introduce a scatter plot tool (AAScatterPlot) that easily shows the selectio

260 scater provides a rich suite of plotting tools for single-cell data and a flexible data

261 The naive solution of simply plotting two-dimensional graphs for every combination of

262 nge of distribution on a two-dimensional(2D) plot upon structural root-mean-square deviations(RMSD) f

263 We conclude that funnel plots using the SMD in combination with the SE are unsui

264 ditionally mean angular error maps were also plotted using automated cross-correlation based approach

265 ting longer survival, than Spartina or mixed plots, vegetation type had no effect on rates of accreti

266 ha to 1.0-ha plots) provided a comparison of plot versus field performance.

267 Pt measured at 600 degrees C form a volcano plot versus relative oxidation potential.

268 he ET rate constants and the maximum VOC are plotted versus the LUMO energy of the acceptor organic m

269 The calibration plot was achieved over the concentration range 1.4x10(-5

270 One plot was amended 16 years ago with process sand, organic

271 gypsum, and seeded (fully treated), another plot was amended 16 years ago with process sand, organic

272 s for the tumor and brain, whereas the Logan plot was appropriate for muscles.

273 putative biomarkers from OPLS-DA model and S-plot was combined to jack-knife confidence intervals, me

274 A forest plot was constructed of the percentage RC estimates from

275 and seeded (partially treated), and a third plot was left untreated.

276 levation dynamics, vegetation in half of the plots was subjected to freezing (mangrove) or wrack buri

277 molecular mechanism based on the van't Hoff plot were examined.

278 n differences obtained from the Bland-Altman plots were 48.5, 47.2, 19.5, and -253.3 cm(3), respectiv

279 Forest plots were created based on Cox model analysis.

280 Experimental plots were established in spatially equivalent positions

281 rrelation coefficient (ICC) and Bland-Altman plots were used to assess the agreement between photogra

282 Concordance indices and calibration plots were used to evaluate the performance of nomogram.

283 Conditional Q-Q and fold enrichment plots were used to visually demonstrate the strength of

284 ctions free/BR follow characteristic sigmoid plots when represented versus redox potential suggesting

285 ce yields were measured for soil replacement plots where the soil was exchanged and adjacent control

286 the soil was exchanged and adjacent control plots where the soil was not exchanged.

287 adelta(37)Cl versus Deltadelta(13)C) isotope plot, which opens further possibilities for pathway iden

288 netic properties by means of catalytic Tafel plots, which relate kinetics and overpotential.

289 quantification, such as the Logan reference plot with 100-min scan time.

290 oncordance was assessed from a four-quadrant plot with a 15% zone of exclusion.

291 on ontology classes, and displays a scatter plot with two proposed new bibliometric statistics: Impo

292 tem functioning (BEF) relationships in small plots with model communities established from species po

293 At the hectare scale, plots with more N-fixing trees grew slower.

294 es from a large-scale network of 447 1-km(2) plots with remotely sensed indices of primary productivi

295 gns using two treatments: trenched plots and plots with shrubs.

296 8 ecosystem functions measured on 209 forest plots) with a forest inventory dataset (105,316 plots) t

297 The results were plotted within a framework formed by an MRI atlas of the

298 soil CO2 flux and microbial community in the plots without litters showed limited response to rains.

299 Here we use data from 3,035 sampling plots worldwide, to quantify the interim reduction of bi

300 nd nearly 2.4 million trees across 24 forest plots worldwide, we show that global patterns in tree sp