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1 ns with known collisional cross-sections for calibration.
2 esearch and minimize the need for repetitive calibration.
3 and 30-day mortality, respectively) and good calibration.
4 x effects that were observed during external calibration.
5 suggesting improvements in engine design and calibration.
6 cross a large number of laboratories without calibration.
7  good discrimination (C-statistic, 0.73) and calibration.
8 iscrimination (c-index 0.89 [0.85-0.93]) and calibration.
9 gether with temperature sensing for internal calibration.
10  to enable rapid detection and avoid tedious calibration.
11  streamline data extraction, processing, and calibration.
12 strated and effectively corrected by routine calibration.
13 aluated using measures of discrimination and calibration.
14 eclassification indices without detriment to calibration.
15 chieved for all samples using matrix-matched calibration.
16 ed heritability estimation, enabling correct calibration.
17 nd biogeographic scenarios with fossil-based calibrations.
18  field (3), resolution (4), scale (3), color calibration (2), and image storage (1).
19 voir by measuring HIV DNA, requires external calibration; a common choice of calibrator is the 8E5 ce
20 rnal discrimination (C-index, 0.77) and good calibration across risk groups as well as accurate predi
21 road taxon sampling (119 taxa) and 18 fossil calibrations across all Cyanobacteria and photosynthetic
22 F5529LP microcontroller to implement an auto-calibration algorithm tailored to improve the detection
23 ion for prediction of detergent was 0.94 for calibration and 0.93 for validation, using partial least
24 uare error (RMSE) from 3250 samples used for calibration and 868 used for external validation.
25                               Matrix-matched calibration and a recovery study were carried out in the
26 or the analysis of different molecules, HPLC calibration and analysis, and data quantification and in
27  models had limited applicability and lacked calibration and clinical implementation data needed to s
28 orrectly classify >99% of the spectra during calibration and cross-validation and to correctly predic
29              Overall, this model showed good calibration and discrimination (C-statistic=0.84).
30  detection technique which requires frequent calibration and has a long response time.
31 e the method, and validation R(2) for simple calibration and PLS were calculated as 0.989 and 0.951,
32 n contrast, digital PCR requires no external calibration and potentially provides 'absolute' quantifi
33            In this manuscript, we describe a calibration and prediction framework for stochastic comp
34 ct classifications were 96% and 100% for the calibration and prediction steps, respectively.
35 d that may improve on current approaches for calibration and prediction using stochastic models of ep
36 cker plant were analyzed using both external calibration and standard additions methods.
37 s the first effort to rely on Bayesian model calibration and synthesis to elucidate the key physiolog
38 ples were quantified applying matrix-matched calibration and using 2-chloro-5-bromoanisole as surroga
39 ion to technical issues regarding instrument calibration and validation and electronic transfer and s
40 ble to correctly classify all samples in the calibration and validation data sets, providing 100% pre
41 f determination values was obtained for both calibration and validation data sets, which are 0.990 an
42 and 0.79, and RMSE of 0.86 and 0.94% for the calibration and validation dataset, enabling quantificat
43   This tool has excellent discrimination and calibration and was validated in a different cohort from
44 g and eliminates the requirement for thermal calibrations and cycling programs.
45  of the models was evaluated with respect to calibration, and area under the curve (AUC) of receiver
46 hours cutpoints were assessed for model fit, calibration, and discrimination separately for the outco
47 wing Ti emissions at 390.11nm for univariate calibration, and partial least square (PLS) calibration
48 equations by assessing model discrimination, calibration, and the net reclassification index.
49 ilable metrics for assessing discrimination, calibration, and the relative performance of different p
50 real-time monitoring enabled by this offline calibration approach can be useful as a key component of
51 t high pressures and temperatures where this calibration approach is unsuitable.
52 dization is carried out by using a two-point calibration approach.
53 ents, we introduce computational methods and calibration approaches that enable rapid and accurate im
54             Because biomarkers available for calibration are limited, most investigators use self-rep
55                   Considering matrix-matched calibration as quantification technique, the recoveries
56 ficial serum sample, the slope of the linear calibration at the relevant background of interfering io
57          The protocol details preparation of calibration bead slides designed for SIM-based experimen
58 y and across ICUs for benchmarking, with low calibration bias.
59                          The use of separate calibrations built by separating hard and soft wheat, or
60 lso promoted assay consistency and minimized calibration burden; analyte response curves were shown t
61 sources of variability to be included in the calibration by minimizing the consumption of API and oth
62              Further, it demonstrated that a calibration can be generated on the offline feed frame t
63 ke risks in all 3 samples than the old FSRP (calibration chi(2) of new/old FSRP: in men: 64.0/12.1, 5
64                                              Calibration coefficients for linear regressions of obser
65 instrument setups by using a suitable set of calibration compounds.
66                                              Calibration conditions are optimized for high dynamic ra
67 39)Ar ages for refining both the radiocarbon calibration curve and the Late Pleistocene time-scale at
68                   The results showed that Ti calibration curve at 390.11nm provides successful determ
69                                          The calibration curve for chlorpyriphos and prophenofos was
70                                            A calibration curve for S(2-) ion estimation has been cons
71                          Importantly, the pH calibration curve is independent of the probe concentrat
72 g, Ca, Na and K) through LIBS was done using calibration curve method in which all calibration curve
73 s per plate run, in the standard addition or calibration curve mode, respectively.
74 rformances such as, for example, R(2) of the calibration curve of 0.98 and 0.99 for proteins and smal
75                                          The calibration curve of lactose using optimized parameters
76 ological range 6.5-7.6 to construct a linear calibration curve of log(CEST104 ppm/CEST64 ppm) versus
77                     Unlike a FET sensor, the calibration curve of the BJT sensor is independent of ap
78 entified and quantitated on the basis of the calibration curve over the range of low ppm to over 100
79 xtraction steps, the method yielded a linear calibration curve ranging from 1.0 to 500mugL(-1) with a
80  using calibration curve method in which all calibration curve shows good linearity (r>0.95).
81                                       With a calibration curve taking into account the CCS dependence
82 dices, delineate the necessity of creating a calibration curve to adjust the given NTA particle numbe
83                                            A calibration curve was constructed on the basis of the su
84                                            A calibration curve was created by measuring the reaction
85                                          The calibration curve was found linear over a wide linear dy
86 in the rhizosphere of experimental plants, a calibration curve was generated that gave the nitrate co
87                                          The calibration curve was linear in the concentration ranges
88                                          The calibration curve was linear in the range 0.5-10mgl(-1).
89  calibration, and partial least square (PLS) calibration curve was obtained by evaluating the whole s
90                                              Calibration curve was obtained by following Ti emissions
91                                     A linear calibration curve was obtained from 0.040 to 1.30molL(-1
92                                            A calibration curve was obtained with a linear range of 0.
93 process efficiency, accuracy, precision, and calibration curve was underscored by calculations perfor
94 e buffer and spiked serum samples provided a calibration curve with R(2) values of 0.97 (n=27) and 0.
95 tion of free hemoglobin, based on a built-in calibration curve, and reports the patient's hemolysis l
96 ectrometry-based assay utilising a universal calibration curve.
97 d is simple, fast (<12.0min), present linear calibration curves (r(2)=0.995), and relative standard d
98                                 Also, sensor calibration curves are impacted by the transducer choice
99                                      We show calibration curves at the femtomolar level for cobalt, n
100 t rely on calibrants, internal standards, or calibration curves but, rather, leverages the relationsh
101 including the necessity to generate separate calibration curves for each biomarker.
102      The immunoassay was utilized to produce calibration curves for quantifying alpha-l-fucosidase co
103 ric acid concentration is known and separate calibration curves have been made for all possible acid
104 ne separation within <3 min, defining linear calibration curves in the range of 0.10-5.0 mmol L(-1).
105                             The matrix match calibration curves showed good linearity (r0.994) over a
106                Under optimum conditions, the calibration curves showed high levels of linearity (R(2)
107 alculated limits of detection (LOD) based on calibration curves were 1.42, 1.00, and 1.34 ng/mL, resp
108                                       Linear calibration curves were obtained for analyte concentrati
109                                       Linear calibration curves were obtained in the concentration ra
110                                          Two calibration curves were prepared from the data obtained
111                               Matrix matched calibration curves were used to determine Fusarium toxin
112 e spiked in aCSF is approximately 1 muM, and calibration curves with internal standards can achieve a
113                 Each approach yielded linear calibration curves with R(2) values between 0.98-0.99 fo
114 mL(-1) and 0.005-100ngmL(-1) for DPV and EIS calibration curves, respectively.
115 f the peak maximum) leading to any number of calibration curves.
116 allows for quantitative assessments based on calibration curves.
117 tal analysis stage, requiring matrix-matched calibration curves.
118  which eliminated the need for predetermined calibration curves.
119 elative standard deviation of the individual calibration data points, measured on immunosensors fabri
120  (bootstrapping) to propagate uncertainty in calibration data through all data manipulation steps.
121 ting the training data with patient-specific calibration data, consisting of an individual's labeled
122 or SIM-based experiments, the acquisition of calibration data, the documentation of typically encount
123 ew and checklist for experimental design and calibration decisions, and is applicable to any commerci
124 Root mean square electromyography/bite-force calibrations determined subject-specific masseter and te
125 actively adapt to them will require regional calibration, due to geographic variation in insect sensi
126 ematic effects removal; iv) investigation of calibration effectiveness using chemometrics methods; an
127 event and those who will not and by adequate calibration ensuring accurate prediction of absolute ris
128                                              Calibration equations did not capture dependencies on bo
129 uation factors, correlations with truth, and calibration equations for FFQ-reported intakes of energy
130           Numerical simulation revealed that calibration error is only negligible when the normalized
131 an area under the curve of 0.819 and average calibration error of 2.7% (95% CI, 2.0%-3.6%).
132        The main outcome was the average risk calibration error.
133 s to provide a check on the maximum expected calibration error.
134  is effective while height/area-based linear calibrations fail, e.g., when (a) the detector is in a n
135 lized root-mean-squared error (NRMSE) in the calibration falls below 0.05%.
136       On the other hand, the external ED-XRF calibration for elements with Z > 20 in acid extracts wa
137               We measured discrimination and calibration for prediction of violent offending at 1 yea
138                         SHFM showed adequate calibration for survival but overestimated LVAD-free sur
139 emonstrated moderate discrimination and good calibration for the prediction of in-hospital and 30-day
140 nge, sensitivity and application of internal calibrations for IgE and IgG4 were assessed.
141 file was then assembled for each point using calibrations for these surface conditions.
142                                      Derived calibrations for total-GSLs, aliphatic-GSLs, glucoraphan
143 des inherent immunity to power fluctuations, calibration-free operation, and an output that is linear
144 ) QEPAS that can be used for ultra-sensitive calibration-free trace-gas detection and fast spectral s
145        Under the optimum condition, a linear calibration graph in the range of 4.00-100.00mgL(-1) was
146                     The dynamic range of the calibration graph was 0.03-0.50mumolL(-1) CoQ10, and the
147            Under the optimum conditions, the calibration graph was found to be LOQ-250microgL(-1) (r(
148          Under the optimized conditions, the calibration graph was linear in the range of 0.017-3.0mu
149          Under the optimized conditions, the calibration graph was linear in the range of 0.3-300mugL
150 ality risk predictions were assessed for (1) calibration (graphically) by comparing the agreement bet
151 terms of discrimination (Harrel C index) and calibration (Hosmer-Lemeshow goodness-of-fit test) for p
152                  The model demonstrated good calibration (Hosmer-Lemeshow goodness-of-fit test, P = 0
153 bidity and mortality, and it had appropriate calibration (Hosmer-Lemeshow P = 0.33).
154 lent discrimination (c-statistic, 0.836) and calibration (Hosmer-Lemeshow P = 0.99) and provided a st
155 ength SIL protein were compared for internal calibration (i.e., as internal calibrators) and external
156 (i.e., as internal calibrators) and external calibration (i.e., as internal standards) when quantifyi
157 ed: external standard, standard addition and calibration in a phenols-free matrix, which was subseque
158 ating HIV-specific covariates exhibited weak calibration in a validation sample and did not discrimin
159 t, 0.78 in validation cohort), with adequate calibration in both cohorts.
160           Under optimum conditions, external calibration in solvent could be used for quantification
161                                        Model calibration in the validation cohort was excellent, with
162 plots showed the new risk score to have good calibration in the validation cohort.
163 s associated with using the 300-Da membrane, calibration in this small size range, accounting for dri
164 enabling, thus, the use of external standard calibration instead of matrix-matched calibration of eac
165                                         This calibration is a critical step to allow interinstrument
166 observing pressure limits are discussed, and calibration is conducted using a combination of bromophe
167 x effects are observed, thus, matrix-matched calibration is required to reach good performances, i.e.
168 roof-of-concept study, through only external calibrations, it was possible to accurately predict the
169 umption of the popularly-used power spectrum calibration method.
170                       Three different ED-XRF calibration methodologies were designed as elemental qua
171 with Z > 20 in acid extracts, a novel ED-XRF calibration methodology based on standard additions was
172  the one hand, the developed external ED-XRF calibration methodology for elements with Z </= 20 was p
173                     Current state-of-the-art calibration methods are generally accurate and applicabl
174  quantitative results were obtained when the calibration mixture was similar to the analyzed sample i
175                Calibration using the general calibration model method resulted in acceptable goodness
176                                              Calibration model was established using the band with a
177                       The performance of the calibration model was evaluated using the coefficient of
178 imperative before calculating a multivariate calibration model.
179 rocedure arises from the need to improve the calibration models prediction ability for cider monitori
180 ) regression was then applied to develop the calibration models, by a new iterative approach.
181 ion analysis (TDA) is an absolute method (no calibration needed) for the determination of the molecul
182 ysis using CN emission band and multivariate calibration NN model obtaining correlation coefficient (
183                                     However, calibration of a model where a behaviour depends on an i
184                           Discrimination and calibration of associations between the mPICH score and
185 s, outlining an all-inclusive method for the calibration of complex magnetic probes with a controllab
186  acoustic effects of muscle recruitment, and calibration of computational birdsong models, enabling e
187 andard calibration instead of matrix-matched calibration of each sample, and the subsequent increase
188 nsights that will be helpful for appropriate calibration of ELISAs.
189 ation in blind people may replace vision for calibration of external space.
190 chosen stellar initial-mass function and the calibration of gas masses) render such comparisons incon
191 tion with high accuracy is crucial for force calibration of optical trapping systems.
192           We validated the accuracy and risk calibration of our model using cross-validation and comp
193 tification and analytical performance is the calibration of the ATR-FTIR sensor which is commonly per
194                                         Mass calibration of the instrument was performed using commer
195 rd and that provided by the astrochronologic calibration of the Oxygen isotopic curves, and to assess
196                                              Calibration of the RDE using a tachometer shows that the
197                              We suggest that calibration of the repulsive exponent in the LJ potentia
198 he Oxygen isotopic curves, and to assess the calibrations of (40)Ar/(39)Ar standards.
199 ectively evaluated screening tools to report calibration or clinical utility for improving health out
200 as evaluated with respect to discrimination, calibration, overall performance, and clinical usefulnes
201                                          The calibration performance for single kernel protein conten
202 ve CT of the L4 vertebral body with use of a calibration phantom.
203                                          The calibration plot allowed a range of linearity extending
204 aluated and discussed in a three-dimensional calibration plot demonstrating the sensor's suitability
205                                          The calibration plot was achieved over the concentration ran
206                     From the gradient of the calibration plot, limit of detection (LOD), and sensitiv
207 ppm MP was achieved from the linear range of calibration plot.
208         Model discrimination was measured by calibration plots and the concordance index.
209                                   The fitted calibration plots exhibit larger coverage with less data
210                                              Calibration plots showed the new risk score to have good
211                      Concordance indices and calibration plots were used to evaluate the performance
212                                           In calibration plots, survival distributions predicted by t
213 er-operator characteristic (ROC) curves, and calibration plots.
214 embrane choices, ionization) and an original calibration procedure allowing the quantification of mas
215           TWIMS and TIMS routinely require a calibration procedure to convert measured physical quant
216 accuracy, advantages, and limitations of the calibration procedures are also discussed.
217 stration, Stokes spectral reconstruction and calibration procedures are included, and the system is v
218 ion of all compounds is achieved by external calibration procedures, and internal quality control and
219                     Hence, BF-QEPAS avoids a calibration process and permits continuous monitoring of
220               Optimization of a multivariate calibration process has been undertaken for a Visible-Ne
221 ractical solutions such as cumbersome signal calibration processes and substantial modifications of t
222 he calibration sample preparation and system calibration protocol can be executed within 1-2 d.
223  the best performance, with a coefficient of calibration r(2) 0.9834 and 0.9775, respectively, and th
224              Large variation occurred in the calibrations, R(2) and RPD due to the variability of the
225 s validated by the in terms of: selectivity, calibration range (0.01-0.05 to 0.5mg/kg), linearity (r(
226      The PE/AgNPs-OA exhibited a wide linear calibration range from 1.7 muM to 30 mM for the determin
227 t the method developed here is linear in the calibration range; recoveries from mouse tissues were in
228 orrections and quantifying with surface area calibration, rather than mass, shows considerably improv
229                           Further aspects of calibration, recoveries, and potential matrix effects ar
230 antitative sensing measurements with minimal calibration requirements, an important characteristic fo
231 or of 18.7% and 32.8% for PLS and univariate calibration, respectively.
232                                   Laboratory calibration results indicated that the thin film retract
233 , and the relative Root Mean Square Error of Calibration (RMSEC) 0.594 and 0.699.
234                                          The calibration sample preparation and system calibration pr
235                                          The calibration scans confirmed that imprinted probes enable
236  faster for the larger analytes studied, and calibration sensitivity is improved by up to approximate
237                                        For a calibration set, there is a single height- or area-based
238                  Comparisons to existing BLM calibrations show good agreement, but reveal that select
239 ighly dense compounds, with traditional mass calibration showing an average error of 34.7% and the ne
240 of 34.7% and the newly proposed surface area calibration showing an average error of 5.8%.
241                                          The calibration slope was 0.9966 (P = .99), determined from
242 9 externally) and high internal and external calibration (slopes 0.71-1.31 between observed and estim
243 s (stage 1) to partial (stages 2-4) and full calibration (stage 5), 24 process-based biogeochemical m
244                                          Two calibration stages were explored, partial (P1), where ex
245                                Partial model calibration (stages 2-4) markedly reduced prediction err
246                                      Using a calibration standard fabricated in our lab to test our p
247 termined from five measurements of the mixed calibration standard were 3.3, 5.3, and 5.4%, respective
248 d for absolute quantification if appropriate calibration standards are used.
249 icroparticles concentration in solution, two calibration standards were used: Virus-Like Particles (V
250 characterized for quantitative imaging using calibration standards, similar calibration tools for imm
251                                              Calibration statistical descriptors on milk dried on pap
252                         This paper describes calibration strategies in laboratory conditions that can
253 membrane TBA(+) ion content was predicted in calibration studies to within a few percent of the conve
254 esults showed that the one-calibrant kinetic calibration technique can be used for determination of c
255    In open bed form, a one-calibrant kinetic calibration technique was accomplished by loading benzop
256  Component Regression (PCR) were used as the calibration techniques.
257                                        First calibration tests show sensitivities of up to 18000 coun
258  Our equations had better discrimination and calibration than the UK Prospective Diabetes Study Outco
259                          The method produces calibrations that are comparable to the state-of-the-art
260  standard solutions can be used for external calibration, thereby significantly increasing the applic
261 lopment of near-infrared spectroscopy (NIRS) calibration to determine individual and total glucosinol
262                                        Model calibration to experimental results allowed estimating b
263                                We expand our calibration to high ligand concentrations and high numbe
264                                The impact of calibration to international units/ml (CMV and EBV) on v
265 dges at both ends, which may provide a great calibration tool for pressure sensors for operation in t
266      We present a non-destructive analytical calibration tool to allow quantitative assessment of ind
267 imaging using calibration standards, similar calibration tools for immunofluorescence with small orga
268 tup achieved stable analyte response and, in calibration trials, a linear response range and detectio
269                         It is limited by the calibration uncertainties in strain amplitude and relies
270               Proteoform Suite performs mass calibration using high-scoring top-down identifications
271 lytical chemistry including (a) multivariate calibration using microwave resonance spectroscopy for t
272                                              Calibration using the general calibration model method r
273                                              Calibration using the quantum simulation data did not pr
274                                      Several Calibration/Validation (Cal/Val) studies for CALIOP cond
275                                          The calibration was analyzed using coefficient of determinat
276                                              Calibration was assessed by comparing observed vs predic
277                                   The sensor calibration was carried out in a high-fidelity aerospace
278                             The multivariate calibration was carried out using a combination of diffe
279                        A near-infrared (NIR) calibration was developed using an efficient offline app
280                                     The NIRS calibration was established based on modified partial le
281       The design of experiment (DOE) for the calibration was established by an initial risk assessmen
282                                              Calibration was evaluated using the Hosmer-Lemeshow test
283  0.76 (95% confidence interval, .71-.80) and calibration was good (Hosmer-Lemeshow C-statistic = 5.48
284 mprovement of analytical results by external calibration was necessary.
285                                              Calibration was not reported despite being a key model p
286 ROC area under the curve=0.62; P=0.122), but calibration was poor, underestimating survival across ti
287 istic, 0.78 for women and 0.79 for men), and calibration was reasonable.
288                                              Calibration was satisfactory, but discrimination ranged
289 C-MS/MS method using authentic standards for calibration was within +/-17%, permitting its use in pre
290                            After a series of calibrations, we site-specifically labeled alpha-tubulin
291                           Discrimination and calibration were also evaluated with these sex-specific
292 th of field, resolution, and scale and color calibration were obtained by the clinical photographer,
293                               Three kinds of calibration were used: external standard, standard addit
294                             The Multivariate calibrations were developed and proposed for Saturated F
295                                              Calibrations were performed by partial least squares reg
296                         High pressure sensor calibrations were performed in standard solutions as wel
297               Single-point internal standard calibrations were used to estimate absolute concentratio
298 tor analyses, including item response theory calibration, were performed; reliability estimates were
299 hod evaluation was done by external standard calibration with linearity range between 0.5 and 3mg/kg,
300 l performance, but with differences in their calibration, with some biased toward higher precision an

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