ライフサイエンスコーパス: current method

1 rovement in sensitivity compared to the best current method.

2 s, demonstrating significant advantages over current methods.

3 ield, while also highlighting limitations of current methods.

4 analysis on a scale that is prohibitive with current methods.

5 eus is difficult to investigate in vivo with current methods.

6 tainties have not been taken into account in current methods.

7 ated at a scale that cannot be achieved with current methods.

8 of single-molecule kinetics beyond those of current methods.

9 lkene intermediates not easily accessible by current methods.

10 ion to relax the linkage phase assumption of current methods.

11 rase chain reaction amplification process of current methods.

12 horter time scale and lower cost than by the current methods.

13 pkCSM performs as well or better than current methods.

14 mans is hindered by technical limitations of current methods.

15 enetration depths than those achievable with current methods.

16 ithout evidence of prior clustering based on current methods.

17 epresenting a more than 20% improvement over current methods.

18 numbers of CD103(+) DCs can be isolated with current methods.

19 than the reliance on serendipity apparent in current methods.

20 ure that bypasses the issues associated with current methods.

21 es at scale and resolution out of reach with current methods.

22 (5) gauss, too low to be detectable by other current methods.

23 Current methods achieve low label enrichment in proteins

24 Few current methods allow single-cell measurement without re

25 However, current methods analyse the complete set of read-derived

26 55% of olive oil were also analysed with the current method and added to the data sets for chemometri

27 of the thermoelectric performance beyond the current methods and approaches.

28 APs is a considerable improvement over other current methods and further facilitates the inference of

29 ed variance, highlighting the limitations of current methods and models and the need for new research

30 However, current methods are complex, lack robustness and do not

31 urthermore, data normalization procedures of current methods are either not suitable for counts or no

32 However, current methods are far from being sufficiently reliable

33 Current methods are highly adapted to a certain biologic

34 phenotypic diversity observed in nature, yet current methods are impractical for characterizing the m

35 However, current methods are imprecise in delineating lesion exte

36 e information on biofilm area are needed, as current methods are indirect and inaccurate.

37 of variability are not well understood, and current methods are ineffective at capturing these detai

38 Current methods are invasive, non-sensitive, non-predict

39 ntal to understanding genomic fragility, but current methods are limited in versatility, sensitivity

40 yrophoric and air-sensitive reagents and the current methods are mostly restricted to organic halides

41 However, current methods are non-quantitative and have important

42 cal applications involving this pathway, but current methods are nonselective and are not applicable

43 Indeed, current methods are not able to predict the presence of

44 Still, the current methods are not optimized to estimate cruise emi

45 However, the efficiency and reliability of current methods are still lagging far behind human perfo

46 Current methods are still not practical for real data sc

47 However, current methods are suboptimal in providing high-speed a

48 nome-wide association study (GWAS) data with current methods are the lack of availability of individu

49 Heavy metals require careful monitoring, yet current methods are too complex for a point-of-care syst

50 areful monitoring due to their toxicity, yet current methods are too complex or bulky for point-of-ca

51 However, the current methods are unsuitable for growing single crysta

52 lated positions (DMPs) cannot be called with current methods as determined by saturation analysis.

53 The accuracy of current methods at genome scale significantly drops with

54 ng microalgae presents an advantage to other current methods available because all materials involved

55 Current methods based on optimization techniques are str

56 However, diversity is hard to estimate by current methods, because of inherent uncertainty in the

57 variations as causal anchors, which improves current methods by taking into consideration hidden conf

58 However, current methods cannot distinguish between inflation fro

59 lenges for delivery of protein therapeutics; current methods cannot quantify the functional effects o

60 to investigate metabolites in single cells, current methods commonly isolate and sacrifice cells, in

61 While the current methods demand high energy consumptions in conce

62 ne but quantification is problematic because current methods depend on indirect measurements at low r

63 step in structure-guided drug discovery, but current methods do little to suggest which interactions

64 Current methods do not adequately address the issues con

65 Current methods do not allow for POC applications due to

66 Current methods do not enable precise engineering of com

67 However, current methods do not scale up well to large sample siz

68 Current methods don't adequately address this issue sinc

69 However, in current methods, efficient acceleration is achieved only

70 Current methods either do not rely on a formal descripti

71 Current methods employed for the analysis of the chemica

72 Current methods enable targeting based on marker gene ex

73 re put at risk during playback, which is the current method for identifying degraded tapes.

74 The current method for removing the cell-cycle effect is una

75 Current methods for 2-DCB extraction are either time-/so

76 Current methods for 4C-Seq analysis only identify intera

77 Current methods for analyzing adaptive immune receptor r

78 Current methods for analyzing root biology balance physi

79 Most of the current methods for analyzing root growth require either

80 Current methods for analyzing systems-level BNs deal wit

81 Unfortunately, current methods for analyzing the SOP fail to account fo

82 Current methods for ancestral reconstruction are limited

83 Current methods for annotating and interpreting human ge

84 hylation data, REPTILE greatly improves upon current methods for annotation of enhancers across a var

85 s for angiosperm phylogenetics projects, but current methods for annotation, alignment and tree estim

86 However, current methods for assessing Hi-C data reproducibility

87 Current methods for automated metabolic network reconstr

88 ology, nanotechnology and biotechnology, but current methods for autonomously synthesizing arbitrary

89 Current methods for cell isolation from complex samples

90 but it also presents an opportunity to test current methods for chemical synthesis and provides an i

91 and critically review each component of the current methods for CNT quantification including CNT ext

92 Current methods for constructing amide bonds join amines

93 Current methods for constructing N-N bonds have limited

94 Current methods for creatinine quantification suffer fro

95 method represents a marked improvement over current methods for detecting and measuring concentratio

96 Current methods for detecting disseminated tumor cells i

97 performance competitive with or superior to current methods for detecting germline and somatic singl

98 However, current methods for detecting viral infections and antiv

99 Current methods for detection and diagnosis of allergies

100 Current methods for detection of copy number variants (C

101 Current methods for diagnosis and monitoring are relativ

102 Current methods for discriminating lymphocyte cell types

103 tion in computational and cognitive systems, current methods for doing so in practice are computation

104 Current methods for dynamically quantifying transduction

105 near, multivariable AFT modeling outperforms current methods for estimating individual survival after

106 However, current methods for evaluating AAV particle populations

107 Current methods for evaluating adipose tissue function a

108 Current methods for evaluating persistence are based on

109 ironment is often unclear, in which case the current methods for evaluating persistence can be questi

110 Current methods for examining mechanical force generatio

111 Current methods for examining NF-kappaB activation invol

112 Yet current methods for examining protein dynamics either ne

113 sulin independence in selected patients, yet current methods for extracting islets from their surroun

114 However, current methods for extraction and measurement of PFCs r

115 chnique makes it an appealing alternative to current methods for fabricating selective solar absorber

116 between their high structural complexity and current methods for fluorination.

117 Current methods for gap filling either fall into the net

118 x (GCC) thickness may be more sensitive than current methods for glaucoma diagnosis and research.

119 A limitation of current methods for human B cell culture is the capacity

120 As current methods for identification of co-expression cann

121 Current methods for identifying in vivo targets of an RB

122 Current methods for identifying TADs using Hi-C data ass

123 Current methods for inspecting protein-detergent complex

124 Current methods for intraoperative histology are time- a

125 tudying lipid metabolism in green algae, but current methods for isolating mutants of this organism w

126 Current methods for magnetizing cells use artificial MNP

127 Current methods for mapping RNA-RNA interactions have to

128 However, current methods for measurement of ammonia are spectroph

129 Current methods for measuring DNA repair capacity (DRC)

130 In this statement, we review current methods for measuring these species and the seco

131 However, most current methods for miRNA detection require lengthy samp

132 ential to cellular differentiation; however, current methods for modeling methylation dynamics do not

133 The invasive nature of the current methods for monitoring of intracranial pressure

134 Most of the current methods for mutagenesis involve multiple step pr

135 Current methods for noninvasively imaging tumor perfusio

136 Current methods for pathogen detection in the clinical l

137 Current methods for predicting adverse events in patient

138 Current methods for producing immunoglobulin G (IgG) ant

139 nsitive, reproducible, and an alternative to current methods for quantitative analysis of blood monos

140 Current methods for rapid detection of delayed graft fun

141 Current methods for reconstructing dynamic regulatory ne

142 Current methods for selective protein degradation requir

143 This model improves upon current methods for separating specific and nonspecific

144 Current methods for sgRNA design are mainly concerned wi

145 However, current methods for single cell isolation struggle to ph

146 However, many current methods for ssRNA-seq suffer from the underrepre

147 Current methods for studying airway obstruction are inad

148 Current methods for studying lysine-based polyubiquitina

149 Current methods for subclone hierarchy inference tightly

150 The current methods for targeted drug delivery utilize ligan

151 However, current methods for TCR inference from scRNA-seq are lim

152 However, current methods for TD identification demand extensive c

153 lts suggest that the MDSeq often outperforms current methods for the analysis of gene expression mean

154 Current methods for the detection of heavy metals requir

155 Current methods for the detection of Mycobacterium tuber

156 Unfortunately, all current methods for the syntheses of these compounds onl

157 Most of the current methods for the synthesis of boronic acids, howe

158 However, current methods for their functional reconstitution in b

159 Current methods for their prevention include avoidance o

160 Current methods for tracking GPCR signaling suffer from

161 Current methods for trapping and analyzing sulfenic acid

162 -specific regulation of gene expression, but current methods generally require large numbers of cells

163 The current method has showed some limitations in elucidatin

164 larly helpful for the hard targets for which current methods have a low accuracy while human-expert k

165 Although current methods have mostly focused on analyzing bacteri

166 Current methods have not yet satisfied the need for rapi

167 merous insights into biological systems, but current methods have several limitations.

168 Using current methods, however, it is laborious and sometimes

169 ing sequences sampled serially through time, current methods implicitly assume either that sampling t

170 The current method improves on previous strategies in that i

171 ion factors and show that DeFCoM outperforms current methods in determining bound and unbound motif s

172 Here we review current methods in human neuroscience, highlighting the

173 r on detecting deletions compared with other current methods in terms of F-score.

174 n, we have shown that our method outperforms current methods in terms of statistical power while main

175 vidence that (18)F-FDG PET/CT may improve on current methods in this regard.

176 Current methods ineffectively capture pathogenic non-cod

177 The current methods involving polymerase chain reaction and/

178 The current method is capable of riboflavin peak % relative

179 The majority of current methods is based on immunological targeting of a

180 s per minute-more than 200 times faster than current methods-is achieved.

181 mapping reads, a time-consuming step in all current methods, it provides quantification estimates mu

182 Current methods lack high sensitivity to detect small tu

183 Current methods limit the biological contexts that can b

184 We found current methods limited in the size of correlated gene s

185 variability to overall phenotypic variation, current methods may miss important links between genotyp

186 oper normalization of metabolomics data, but current methods may not be applicable when estimating in

187 Yet, current methods merge the sequence space and the structu

188 t produce H2 in monoculture, indicating that current methods might not adequately estimate the thermo

189 cations to oncology, critical limitations of current methods must be addressed.

190 Multiphoton microscopy is the current method of choice for in vivo deep-tissue imaging

191 The current method of choice predicts transcription factor (

192 The current method of controlling selectivity provides oppor

193 n clinical examination or leakage on FA, our current method of diagnosing this important endpoint, wh

194 However, the current method of editing the VACV genome is not efficie

195 The current method of synthesizing these hybrids via direct

196 Current methods of chemical vapour deposition (CVD) of g

197 This review describes the evidence examining current methods of cleaning, disinfecting, and monitorin

198 ediated boundary significant advantages over current methods of concentration and separation and the

199 ts to megacities justify a re-examination of current methods of converting reactive nitrogen to dinit

200 Current methods of detection include ultrasound examinat

201 l sensors and assays offer an alternative to current methods of detection.

202 Growing evidence suggests that current methods of direct lineage conversion may rely on

203 We show that current methods of estimating CTL escape rates, based on

204 Current methods of estimating the public health effects

205 Key points of departure from current methods of expert-based narrative review prevale

206 In contrast to current methods of expert-based narrative review, the Na

207 Current methods of fabricating 3D-shaped particles such

208 Unfortunately, current methods of gene delivery treat only a fraction o

209 In this article we review the current methods of gut microbiome analysis and the resul

210 Current methods of identifying antigen-specific T cell r

211 t issues are associated with a number of the current methods of immobilization.

212 However, current methods of loss-of-function analysis are insuffi

213 Due to the challenges encountered with current methods of lycopene extraction using hazardous s

214 Current methods of measuring DNase I relies either on an

215 Current methods of monitoring breathing require cumberso

216 Current methods of network comparison are limited to ext

217 t holds promise as a powerful alternative to current methods of neural control, which rely predominan

218 Current methods of ocular treatment allow globe salvage

219 ion of the population diversity, challenging current methods of outbreak tracing and resistance diagn

220 e a better physiological representation over current methods of patient-derived cell culture and xeno

221 Current methods of PD-L1 diagnosis have shown to vary ba

222 Current methods of protein delivery commonly suffer from

223 a and represent a potential target to refine current methods of surgical planning and stimulation par

224 Current methods of transporter measurement, however, are

225 Our scheme alleviates several limitations of current methods, offering a new pathway towards direct r

226 Compared with current methods on both simulated and experimental densi

227 In comparison with current methods, our approach tackles the challenges pos

228 ow to high LETs which is an advantage of the current method over methods previously employed to fit t

229 Most current methods perform well on molecular function predi

230 Although current methods permit accurate comparisons of the effec

231 The current method provided precision of less than 6% RSD, (

232 The current method provides a novel method to study the join

233 Moreover, current methods providing such information require exten

234 ar with current assays and, in contrast with current methods, quantitatively scores PPIs with enough

235 Most current methods rely on features that are manually selec

236 Many current methods rely on parameters requiring calibration

237 However, current methods rely on viral identification, and this a

238 Current methods require high-coverage genotype data and

239 However, in current methods, shear waves are measured near the surfa

240 Venn diagrams comparing MUMAL2 with the best current method show that the number of exclusive peptide

241 Overall, our current method successfully addresses the aforementioned

242 However, current methods suffer from interference between the sin

243 Unfortunately, current methods suffer from invasiveness, poor resolutio

244 However, current methods that address this problem assume that ea

245 Y chromosomes, which is a requirement of all current methods that determine stratum structure based o

246 original, specific property information than current methods that operate on homogeneous networks.

247 hment in France showed that, compared to the current method, TNT2-LCA allows delineation of more appr

248 is) can identify complex infections, but the current method to distinguish clonal heterogeneity from

249 tion is a serious public health problem, and current methods to abate addiction and relapse are curre

250 Current methods to analyze urinary iodide are limited by

251 Current methods to assess undesired photo-induced cell c

252 nalytes emphasize the susceptibility of many current methods to blank contamination, misinterpretatio

253 Current methods to control and study receptor function,

254 t on high-quality adherent cell culture, but current methods to cryopreserve cells in this format can

255 Current methods to culture murine MSCs (mMSCs) select fo

256 Because current methods to detect acetylcarnitine involve biopsy

257 Current methods to detect aggregation of biological mole

258 However, the current methods to detect anti-PEG abs are tedious and u

259 Current methods to detect C. difficile spores on surface

260 Current methods to detect carbapenemase activity are sub

261 The current methods to determine the influence of one region

262 a disagree on many of their predictions, and current methods to evaluate accuracy and computational p

263 However, current methods to evaluate mitochondrial activity still

264 been a recent focus on critically evaluating current methods to fill data gaps and on identifying ext

265 Because current methods to generate a stable vortex are difficul

266 Current methods to generate alloantigen-specific Tregs r

267 Current methods to generate amiRNA or syn-tasiRNA constr

268 However, current methods to generate hypomorphic mutations are li

269 Current methods to identify patients at risk for cardiot

270 However, the specificity of current methods to identify simultaneously several cance

271 TFs tend to bind the genome in clusters, and current methods to identify these clusters are either li

272 The current methods to image the distribution of Pt drugs ar

273 Current methods to investigate neuraminidase activity us

274 The purpose of this review is to summarize current methods to measure autophagy, selective mitochon

275 Unfortunately, current methods to measure biomechanical properties are

276 However, current methods to measure cooperativity parameters have

277 However, current methods to measure metabolites are either low-th

278 However, current methods to measure O2 isotope signatures are tim

279 However, current methods to measure RNA polymerase fidelity are l

280 Current methods to measure supracellular mechanical prop

281 Current methods to monitor subsurface biofilm growth in

282 However, current methods to produce amiRNA constructs for silenci

283 This is not trivial because most current methods to simulate Boolean network models of GR

284 ns also presents a substantial challenge, as current methods to store genealogies consume a great dea

285 Current methods to synthesize PG are not sustainable due

286 Current methods toward incorporating lithium in sulfur-s

287 Current methods treat pathways as independent entities.

288 Current methods use database searches that are dependent

289 um parsimony reconciliations is NP-complete, current methods use either exact algorithms with exponen

290 Current methods used to characterize the mechanodynamics

291 while trapping the target cell, because the current method uses long ultrasound pulses for grabbing

292 Current methods using Na(+)-sensitive fluorescent indica

293 Indeed, current methods (using cell-penetrating peptides for ins

294 Most current methods utilizing network information to priorit

295 This finding implies that, with current methods, visual prosthetics will have a limited

296 dual cancer cells and MRD (undetectable with current methods) were non-invasively detected up to 4 mm

297 ids would provide a significant advance over current methods, which often lack specificity.

298 In comparison to current methods, which utilize hydrogen peroxide as an o

299 ffers significantly greater sensitivity than current methods, while computational optimizations reduc

300 However, current methods yield ensemble profiles that are insensi