ライフサイエンスコーパス: plot

1 ted based on 12 plots and 24 samples in each plot.

2 the data in the three-dimensional FSCV color plot.

3 a samples using the conventional calibration plot.

4 d deadwood structure in a 32-year-old forest plot.

5 and GAT was measured using the Bland-Altman plot.

6 med using Deming regression and Bland-Altman plots.

7 ludes an R-Shiny application with diagnostic plots.

8 Publication bias was modeled using funnel plots.

9 ibutions was used, which was based on moment plots.

10 he co-occurrence of variants with comutation plots.

11 sistant isolates in GaM-treated or untreated plots.

12 ted to greater stability in NEE in deep-snow plots.

13 ng patterns of RNA, as visualized by Sashimi plots.

14 ologic nodal stage (ypN0) using Kaplan-Meier plots.

15 under the curve (AUC) and decile calibration plots.

16 report of informative statistical tables and plots.

17 ivation energies of diffusion from Arrhenius plots.

18 novel discoveries through easy-to-understand plots.

19 Inventory and Analysis data from 989 burned plots.

20 nsused on > 1000 trees in nine 0.1 ha forest plots.

21 antitative performance comparisons as master plots.

22 sed in FYM plots compared to the rest of the plots.

23 sponding locations in the X- and XY-distance plots.

24 widely in the numbers and sizes of sampling plots.

25 erved in polyculture relative to monoculture plots.

26 e sites having additional irrigated cropland plots.

27 analysis of linear free-energy relationship plots.

28 plots, scatter plots, histograms and volcano plots.

29 the accuracy of O:C ratios and van Krevelen plots.

30 oup membership was assessed with calibration plots.

31 rings, including county maps and state-level plots.

32 diversity began to increase in unfertilised plots.

33 00 species from 189 long-term RAINFOR forest plots.

34 gating of subpopulations on two-dimensional plots.

35 t type was applied to nine randomly selected plots.

36 n organic soil horizons than heather control plots.

37 N pools were found in grazed and fertilized plots.

38 o artificial widening of DI versus cell size plots.

39 omposition of beetles captured in experiment plots.

40 d using Michaelis-Menten and Lineweaver-Burk plots.

41 reproducibility comparison, and Bland-Altman plots.

42 torical event size) on undisturbed grassland plots.

43 nce spectroscopy and corresponding data were plotted.

44 analysis and dipolar and chemical shift wave plotting.

45 per biological significance test and heatmap plotting.

46 In the Bland-Altman plot, 100% (48/48) of paired values (standard deviations

47 We present Stairway Plot 2, a cross-platform program package for this task u

48 f high-yielding farmers by up to 7% in small plots (8 site-years) and 15% in field-scale comparisons

49 In the Bland-Altman plot, 97.9% (47/48) of paired values (SDs of the CMS and

50 line-based semiparametric model with contour plots, accounting for possible nonlinear relations and i

51 s-based terrestrial ecosystem model to seven plots across a moisture stress gradient with detailed in

52 atography with electrochemical detection and plotted against HR.

53 cores between 0 and 8 weeks of treatment was plotted against PFC and ACC TSPO V(T), showing a signifi

54 The use these specific three-isotope plots allows a non-ambiguous discrimination between auth

55 When plotted along corresponding percentiles, the positive pr

56 Calibration plots also suggest that overestimation increases towards

57 th-hour time frame based on the Bland-Altman plot analysis.

58 igh AMF alpha- and beta-diversity across the plot and at all investigated time points.

59 n be visualized using a pre-calculated t-SNE plot and can be coloured by different features or by cel

60 Publication bias was evaluated via funnel plot and Egger's test.

61 f HMBP-Al(3+) was determined as 1:2 by Job's plot and ESI-MS as well as (1)H NMR titration.

62 of the two-dimensional relative mass defect plot and offers the possibility for a more detailed subs

63 1-hexanol were selected based on the loading plot and their variables importance in the projection (V

64 al of 288 samples were collected based on 12 plots and 24 samples in each plot.

65 tribution images were calculated using Logan plots and analyzed on a volume-of-interest basis.

66 quality control metrics, generate essential plots and carry out analyses.

67 and soil surveys were carried out on ski run plots and compared to paired, undisturbed control sites

68 iability for tree species in 21 large forest plots and found much greater variability for higher lati

69 Correlation plots and intraclass correlation coefficient analysis co

70 surements was assessed by using Bland-Altman plots and intraclass correlation coefficients (ICCs).

71 We performed Bland-Altman plots and scatterplots to assess agreement between equat

72 scovered with RE2C are accompanied by forest plots and standardized predicted random-effects statisti

73 Publication bias was evaluated by funnel plots and the Egger test.

74 hotovoltage decay (OCVD), Mott-Schottky (MS) plot, and transient absorption spectroscopy (TAS) provid

75 ed versions of scatterplot matrices, volcano plots, and litre plots through the implementation of lay

76 lor plots were compared with reference color plots, and the SSIM cutoff score was optimized to distin

77 We identified six plots as originating from planting, rather than natural

78 ble quality control, differential expression plots as well as enrichments and protein-protein interac

79 mation is shown in the form of a genus trace plot, as well as a genus matrix diagram.

80 ng polyculture plots compared to monoculture plots, as well as a distinct species composition between

81 Funnel plot asymmetry and trim-and-fill revealed a clear public

82 alization), using paired grazed and ungrazed plots at 10 locations across the Mongolian Plateau.

83 even long-term bare-fallow (vegetation-free) plots at six sites: Denmark (two sites), France, Russia,

84 e mechanisms by decomposing changes in whole-plot biomass fluxes into contributions from changes in t

85 ropod Tritia neritea, using Bayesian skyline plots (BSP), multivariate analyses and Bayesian clusteri

86 In Kaplan-Meier plots by treatment regimen, those treated with SOF/RBV,

87 ion obtained from IRMPD and EID 2DMS contour plots can accurately identify and characterize agrochemi

88 tiple visualizations, such as k-mer spectrum plots, can be generated for evaluation.

89 Bland-Altman plots, coefficients of repeatability, and Pearson correl

90 ) and FD (25%) of birds visiting polyculture plots compared to monoculture plots, as well as a distin

91 0-10 cm depth significantly increased in FYM plots compared to the rest of the plots.

92 The resulting 2DMS contour plot contains abundant tandem MS information for each co

93 olar coordinates (HR-radius, DeltaPhi-angle) plotting cos(DeltaPhi) versus HR to determine if transit

94 However, the plots cover most of the environmental conditions across

95 -based assessments were conducted across 255 plots covering undisturbed and LULCC-affected mangroves

96 pproach, which provides several functions to plot data and fit models, assess their confidence and co

97 ng a combination of local-scale experimental plot data and geographic-scale data contained within the

98 uctivity between fertilized and unfertilized plots decreasing in proportion to nitrogen addition-depe

99 Bland-Altman plots demonstrated a systematic bias in most individual

100 Funnel plots demonstrated positive publication bias in PPV and

101 s showed notable alignments in binary mixing plots, demonstrating the dissemination of radioactive-en

102 Bland-Altman plots depicted varying agreement across APC platforms.

103 multiple statistics and publication-quality plots describing the quality of the data including N50,

104 th a bare earth control in a three-way split plot design such that the crop in each plot was sprayed

105 visualized using a two-dimensional Manhattan plot, displaying chromosomal location of SNPs along the

106 ics, we conducted a girdling experiment with plots distributed across 1 km(2) of treeline birch (Betu

107 modified Newcastle-Ottawa scale and a funnel plot (effect size measured using Hedges' g followed by t

108 data set, generating a series of interactive plots, EICs for individual components or entire compound

109 raphs can be prepared in TBtools using a new plotting engine ("JIGplot") developed to maximize their

110 regionally replicated 1-ha forest inventory plots established in a region of high geomorphological h

111 Soil plots experimentally infected with Rhodococcus equi (R.

112 Variation in whole-plot fluxes among census intervals was explained overwhe

113 The calibration plot for butralin obtained by square wave voltammetry wa

114 representation of the traditional Manhattan plot for displaying and exploring GWAS data.

115 The calibration plot for tannic acid by differential pulse voltammetry w

116 mal statistical test and a quantile-quantile plot for visualization.

117 We provide novel computed IMS contour plots for a representative selection of aromatic molecul

118 Bland-Altman plots for AbsCD4, CD4%, and Hb levels demonstrated close

119 rally more evident in LN or HN plots than NN plots for BG in SG and CBH in GG.

120 the information presented by separate funnel plots for each outcome while elucidating more complex fe

121 lity figures as well as interactive spectrum plots for inclusion on web pages.

122 image analysis-based analysis of FSCV color plots for the first time, specifically the structural si

123 e class profiling using relative mass defect plots for the visualization of herbal compositions.

124 nalysis, the cumulative response curves were plotted for dichotomized reductions ranging from >=20% t

125 The receiver operating curves (ROCs) were plotted for every measurement and contrasted with the pr

126 We experimentally burned 102 plots, for which we measured vegetation structure, fuels

127 collected soil samples from five replicated plots from "S" shape soil profiles to the depth of 50 cm

128 hanisms of soil bacterial communities in 660 plots from 11 regions along a latitudinal gradient in ea

129 1 countries, compare them with 321 published plots from Amazonia and investigate the underlying drive

130 ented Python package that creates comutation plots from arbitrary input data, including categorical d

131 tomizable and publication quality comutation plots from arbitrary user data.

132 a dynamic visualization combining Manhattan plots from GWAS with PheWAS to create a 3D 'landscape'.

133 Logan plot graphical analysis demonstrated late linearity, sup

134 affected by fertiliser treatment, fertilised plots had a significantly higher abundance of leaf miner

135 The decay of SOC in these plots has been monitored for decades since the last inpu

136 Funnel plots have been widely used to detect small-study effect

137 ions such as line charts, box plots, scatter plots, histograms and volcano plots.

138 habitat, 250 soil cores were sampled from 10 plots hosting 10 different plant families across three f

139 In a 50-ha plot in a subtropical forest, China, we randomly sampled

140 mbinations) were planted in a diseased field plot in the Great Basin Desert of Utah.

141 reality (VR), designed to render a Manhattan plot in three dimensions, wrapping the graph around the

142 tional properties of regeneration across 316 plots in agroforestry parklands of Ghana and Burkina Fas

143 re comparable in unfertilized and fertilized plots in GG.

144 nts (DBE) versus number of carbon atoms (#C) plots in order to observe similarities and differences w

145 alpractice and the proper use of logarithmic plots in representation of calibration data sets.

146 ere 20~77% higher in NN plots than LN and HN plots in SG but they were comparable in unfertilized and

147 rived from over 38 thousand forest inventory plots in the eastern US from 2005 to 2017.

148 tant vector and its confidence interval were plotted in 2-dimensional S-F space.

149 Cluster rank plot incorporating stroke and major bleeding outcomes in

150 The Tafel plots indicate remarkably low charge transfer resistance

151 Bland-Altman plots indicated a very small percentage of results outsi

152 Bland-Altman plots indicated little bias between MeHg measurements wi

153 sed 36 paired invaded and non-invaded sample plots, invaded by the plant Antigonon leptopus, with hal

154 show that Cattell's rule based on the scree plot is a powerful tool to determine the number of cell-

155 The galaxy plot is an intuitive visualization tool that can aid in

156 f isotropic magnetic shielding (IMS) contour plots, is shown to provide a feature-rich picture of aro

157 Inspection of the Bland-Altman plots led to decisive agreement between the two reviewer

158 that N fertilizations generally reduced the plot-level variance and simultaneously re-established sp

159 d that SG generally displayed 10~120% higher plot-level variations in all variables than GG, and the

160 variations in all variables than GG, and the plot-level variations were 20~77% higher in NN plots tha

161 DNA Features Viewer is a sequence annotation plotting library which optimizes plot readability while

162 From the calibration plot LODs were calculated to be 0.032 ug L(-1) (Cd(II))

163 Here, we analyze 590 permanent plots measured across the tropics to derive the equilibr

164 The package provides a suite of plotting methods and enables expedient, flexible and int

165 ats" module), generating informative plots ("plotting" module), identifying lipid species at differen

166 database and a long-term continental forest plot network to map changes in community trait distribut

167 tive analysis was achieved using calibration plots obtained from fortified meat samples.

168 From a Tauc plot of (alphahnu)(2) versus energy, the direct band gap

169 A novel phase-behavior viscosity map-a plot of added salinity vs. soap fraction combining phase

170 racting fragment, yielding a high-resolution plot of the binding interface.

171 An Ashby plot of the CTE versus density serves as a quantitative

172 A semi-logarithmic plot of the dimensionless numbers indicated the emergenc

173 A plot of the interaction demonstrated that AC was associa

174 ies; a well-known illustration is the zigzag plot of their melting point versus chain length.

175 rs, forming 'arrays' which encircle a forest plot of ~30 m diameter.

176 Many enzymes show curvature in plots of activity versus temperature that is not account

177 mutant displays similar breaks in Arrhenius plots of both kinetic and HDX properties that are absent

178 ing for Manhattan distance to create average plots of Hi-C and HiChIP data.

179 3 m depth in eight sites, each having paired plots of native vegetation and rain-fed croplands, and h

180 me intervals between detections, and scatter plots of peak frequency, RMS, and peak-to-peak received

181 The plots of phase angle and LBI as a function of data point

182 Finally, abundance plots of selected analytes from the tricarboxylic acid c

183 Scatter plots of TD-CRDS and SMPS data correlated (r(2) > 0.9) w

184 isualize function initiates a dashboard with plots of the relevant QC outcomes.

185 gorithm-agnostic interactive exploration and plotting of gene fusions.

186 posterior capsulotomy rate for each lens was plotted on a monthly basis for the same period, creating

187 Methyl anion affinities (MAA*), plotted on the log scale of Mayr E, provide insights int

188 and those that do have been conducted within plots or mesocosms.

189 minated from each other, visually with t-SNE plots or quantitatively with the Gene Oracle deep learni

190 patients and 35.6% in controls (Kaplan-Meier plots, P = .005).

191 e differed with N fertilization due to large plot-plot variation.

192 ses ("stats" module), generating informative plots ("plotting" module), identifying lipid species at

193 n of the theoretical two-dimensional volcano plot predicted for L1(0)-CoMPt.

194 tronic properties of a molecule, IMS contour plots present a detailed, global landscape of a molecule

195 The resulting novel relative mass defect plots provide a quick way of two-dimensional substance c

196 = 28.9%; Q = 18.27, P = .16), and the funnel plot provided no evidence for publication bias.

197 This traditional plot provides a broad overview of the results, but offer

198 of 300 Omega cm(2) obtained from the Nyquist plot provides an insight into the rate of charge transfe

199 Funnel plot, Q statistics, and I(2) were used to test the heter

200 ed bioplatform exhibits a linear calibration plot ranging from 1 to 200 IU mL(-1) with a LOD of 0.3 I

201 annotation plotting library which optimizes plot readability while letting users tailor other visual

202 We surveyed 32 plots, recording 2025 trees of 97 species, and 7853 inse

203 oints and protein domains by transcript, and plot recurrent fusions within cohorts.

204 The Bland-Altman plots reported the lowest SUV bias (0.02) and variance (

205 s (LFERs)-including Hammett and Swain-Lupton plots-reveal a clear difference in sensitivity to the po

206 A Bayesian Skygrid plot revealed that the effective population size of HIV-

207 ctions, as suggested by multivariate loading plots, revealed highly complementary molecular informati

208 atiotemporal variation in AMF diversity on a plot scale (10 x 10 m) in a grassland managed at low int

209 natural vegetation are still lacking at the plot scale.

210 Full-data analyses of the raw plot-scale data using multilevel models were also suscep

211 discerned from remote sensing can complement plot-scale studies of plant physiological responses to d

212 Here we integrate plot-scale vegetation data with detailed climate and sno

213 tive visualizations such as line charts, box plots, scatter plots, histograms and volcano plots.

214 aROC is created by plotting sensitivity against 1-specificity.

215 ant signal of adaptive differentiation among plots separated by < 1 km, with selection acting on grow

216 functions, e.g., managing data, customizing plots, setting parameters, and monitoring real-time resu

217 Star plot show that woody aroma compounds are dominant in win

218 Bland-Altman plot showed a consistent difference between full finger

219 Bland-Altman plot showed mean bias between FFR and CT-FFR as 0.059+/-

220 The typical thoracoabdominal motion (TAM) plot showed the abdomen and rib cage motion in synchrony

221 For the PC1, Kaplan-Meier plots showed a significant difference between PC1 low vs

222 Root-to-tip plots showed the DRC66 sequence is not an outlier as wou

223 ovariation between replication, variance and plot size.

224 using subpopulation treatment effect pattern plot (STEPP) methodology across subpopulations defined b

225 e present study represents the first "Paired Plot" study of the water balance of afforestation on the

226 carbon sink, our most intensively monitored plots suggest a post-2010 increase in carbon losses, del

227 se correlations between guild abundances per plot, suggestive of weak signals of both inter-guild com

228 hurricane were higher in previously managed plots than in un-managed controls.

229 ot-level variations were 20~77% higher in NN plots than LN and HN plots in SG but they were comparabl

230 erns were generally more evident in LN or HN plots than NN plots for BG in SG and CBH in GG.

231 cept user's private bigwig files as input to plot the concerned data on promoters, exons or any other

232 ted Stochastic Neighbor Embedding (t-SNE) to plot the distribution of compounds embedded in a 2D map,

233 Kaplan-Meier curves plot the duration of effect.

234 m according to frequency or tidal volume and plots the results against bin means.

235 We found that, by plotting the accumulative positions of five- and sevenfo

236 es (five-parameter logistic fit p < 0.05) by plotting the measured ratios of the MS ion responses aga

237 ntial log-hazard ratio, the survival scatter plot, the hazard ratio receiver operating characteristic

238 Based on the calibration plot, the quantities of several low concentration HMOs w

239 chanistic model showed that among the forest plots, the net effect of temporal population variability

240 In combination with Hammett plots, these studies document the relationship between o

241 Plotting this transition's local coexistence points agai

242 atterplot matrices, volcano plots, and litre plots through the implementation of layered interactivit

243 earman's) correlations and used Bland-Altman plots to compare GCIPL thickness measurements between th

244 more than 130,000 national forest inventory plots to describe the contribution of nearly 1.4 trillio

245 VALERIE generates an ensemble of informative plots to visualise cell-to-cell heterogeneity of alterna

246 eceiver operating characteristic curves were plotted to evaluate diagnostic performance of renal resi

247 Heat maps were plotted to summarise the topography of rod and cone pigm

248 is includes all the associated visualization plots, to allow ease of data interpretation and manuscri

249 ll as a distinct species composition between plot types.

250 spatially explicit design within two 15-m(2) plots under three fertilization treatments in SG and GG

251 il (0-15 cm) were collected from two 15 m(2) plots under three fertilization treatments in switchgras

252 outcomes of visualization method (silhouette plot) used to compare results of implemented chemometric

253 The Bland-Altman plot, used to compare the 2 measurement methods, showed

254 tooth were ascertained by smoking status and plotted using contour maps to identify new patterns.

255 er of nodes removed and 5-year OS or DFS was plotted using restricted cubic spline functions.

256 Within-plot variances of glycosidases appeared higher in SG tha

257 delta(15)N were quantified and their within-plot variations and spatial distributions were achieved

258 The descending within-plot variations were also identified among variables (SO

259 The Lassen plot was applied to compute levetiracetam occupancy and

260 The occupancy plot was applied to compute receptor occupancy by scopol

261 The plot was characterized by high AMF turnover rates with a

262 Funnel plot was not performed due to the limited number of stud

263 split plot design such that the crop in each plot was sprayed with either a 10% (w/v) aqueous extract

264 Galbraith plot was used to investigate statistical heterogeneity a

265 a decade, and including over 50,000 habitat plots, we examined the panda population and habitat tren

266 ance classes within the relative mass defect plots were calculated.

267 Using SSIM, sample FSCV color plots were compared with reference color plots, and the

268 Thirty-six plots were developed to grow collard greens on Prairie V

269 Study plots were established in 2000 and re-surveyed in 2017 o

270 Arrhenius plots were generated to calculate the respective activat

271 med, and corresponding Kaplan-Meier survival plots were generated.

272 The calibration plots were linear in the range of 10-1000 ug L(-1).

273 catches were reduced in the field more when plots were treated with verbenone dispensers (SPLAT) co-

274 Three random plots were used as a control in each row.

275 elation coefficients (ICCs) and Bland-Altman plots were used to assess intra- and interreader variabi

276 sure discriminative ability, and calibration plots were used to assess the degree of agreement betwee

277 elation coefficients (ICCs) and Bland-Altman plots were used to assess the reliability of the repeate

278 ential functions (f, D(p), D(f)) while Logan plots were used to calculate volume of distribution (V(T

279 nfluence on survival, and partial dependence plots were used to determine the dependence of survival

280 ray ionization (ESI)-mass spectra, and Job's plots were used to verify the mechanism of the specific

281 In the randomized study, the EI scatter plots were visibly separated for the low- and high-elast

282 rever feasible and violin or box-and-whisker plots when not.

283 r(-1) , five of which also have experimental plots where atmospheric N deposition was simulated throu

284 trast, significantly decreased in fertilized plots where herbivores were removed.

285 , e.g., by replacing bar graphs with scatter plots wherever feasible and violin or box-and-whisker pl

286 rris intra-particle diffusion model and Boyd plot which showed that the adsorption process was both i

287 opose a new visualization method, the galaxy plot, which can simultaneously present the effect sizes

288 We illustrate the use of the galaxy plot with 2 case studies, including a meta-analysis of h

289 and retest was established by a Bland Altman plot with 95% limits of agreement.

290 ic network representations, data tables, and plots with comprehensive activity summaries across all T

291 d gas production in soils from tilled arable plots with contrasting fertilizer inputs (no N, mineral

292 much greater variability for higher latitude plots with fewer tree species.

293 viduals occupied higher trophic positions in plots with higher wolf spider densities.

294 elation coefficients (ICC), and Bland-Altman plots with linear regression.

295 tial dependence and accumulated local effect plots with modeled aqueous uranium speciation and surfac

296 Plots with trees had greater soil respiration and lower

297 ggregation to an extended database of forest plots with up-to-date taxonomy.

298 Old soil C loss was suppressed in plots with warmer deep soil temperatures because they te

299 e strata can be explored in a sectional view plotted within user defined levels.

300 also show that using ten times the number of plots would result in an increase to just ~50% of those