ライフサイエンスコーパス: current method

1 lities, which are difficult to obtain by the current methods.

2 ssary: requirements not fulfilled by most of current methods.

3 major sources of confounding not offered by current methods.

4 ronates, which are not readily accessible by current methods.

5 omical production of (15)O compared with the current methods.

6 This is in part due to the limitations of current methods.

7 cryo-EM structures when used in addition to current methods.

8 ercomes some of the bottlenecks limiting the current methods.

9 that, to date, have resisted detection using current methods.

10 However, this is not possible with current methods.

11 ion in side-by-side comparisons with several current methods.

12 ntial to attack problems beyond the reach of current methods.

13 s, demonstrating significant advantages over current methods.

14 ield, while also highlighting limitations of current methods.

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

16 than the reliance on serendipity apparent in current methods.

17 rovide additional survival prediction to the current methods.

18 ure that bypasses the issues associated with current methods.

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

20 ebraic in nature and distinct from all other current methods.

21 t are especially challenging to analyze with current methods.

22 ation of such pulses is still a challenge by current methods.

23 work of the analysis when compared to other current methods.

24 munity vastly exceeds what is feasible using current methods.

25 Current methods(1-4) are limited by the loss of native m

26 Current methods achieve low label enrichment in proteins

27 Current methods allow easy and quick integration of fluo

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

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

30 compare the advantages and disadvantages of current methods and discuss the outstanding challenges a

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

32 We describe optimization of current methods and present new protocols for using HPV

33 While the current methods and procedures for quantitative determin

34 We discuss the limitations and challenges of current methods applied to apicomplexan noncoding RNA st

35 , genome-wide studies of small RNA; however, current methods are challenged by low sensitivity and hi

36 in research and clinical applications where current methods are either too slow or are destructive.

37 cal diagnosis of reproductive disorders, but current methods are hampered by frequent blood sampling

38 cterizing gene expression in eukaryotes, but current methods are incompatible with bacteria.

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

40 However, current methods are insufficient to test hypotheses that

41 We conclude that current methods are largely suitable for the qualitative

42 mportant strategy for their preparation, yet current methods are limited in their alkene-types and to

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

44 Most current methods are limited to identifying mean effects,

45 However, current methods are limited, and the most accurate techn

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

47 Despite many successes, current methods are not able to keep up with the growing

48 It is possible that current methods are not sensitive enough to reveal the e

49 enabled great progress on this problem, but current methods are specialized for images that have lar

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

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

52 mes with the analyses of their hard tissues: current methods are time-consuming, destructive, and lar

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

54 Thus, none of the current methods are utilized as a generally applicable,

55 fferent domains, and how close to optimality current methods are.

56 However, current methods assume plane monolayer geometry and negl

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

58 Current methods based on optimization techniques are str

59 of ampicillin, which would have failed using current methods because it adopts a high-energy conforme

60 s of routinely practiced therapies and three current methods being explored for BBB/BTB disruption fo

61 s way are similar to those generated via the current methods, but with more than five times higher se

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

63 Current methods can illuminate the genome-wide activity

64 But no current methods can integrate heterogeneous prior inform

65 However, current methods cannot estimate single-neuron RF sizes a

66 Current methods cannot join ceramics in proximity to tem

67 However, current methods cannot profile TFs genome-wide at or nea

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

69 While the current methods demand high energy consumptions in conce

70 We observed that current methods designed for scRNAseq data do not tend t

71 Current methods do not adequately address the issues con

72 by covalent tagging of surface glycans, yet current methods do not afford sequencing of intact glyco

73 Moreover, current methods do not allow direct readout of epigeneti

74 Current methods do not enable precise engineering of com

75 For lead, the GBD's current methods do not fully account for lead's impact o

76 In addition, current methods do not provide any indication of the fun

77 r blocks have potential for scalability, but current methods do not scale to mammalian genomes.

78 However, current methods do not utilize endogenous proteins and,

79 Current methods don't adequately address this issue sinc

80 seful pedigree drawing tool that improves on current methods due to its ease of use and approachabili

81 Current methods (e.g. ELISA) for detecting immune-checkp

82 viding accurate and effective care; however, current methods (e.g., blood draws) are inconvenient and

83 Unfortunately, current methods (e.g., electrophysiology) provide limite

84 Current methods either do not rely on a formal descripti

85 the characterization of GSR particles by the current methods employed by forensic experts.

86 The current method enables us to accurately quantitate rapid

87 neous samples are promising, but most of the current methods estimate either cell-type proportions or

88 neering can improve aptamer performance, but current methods exhibit inherent bias and variable rates

89 man genes having more than two APA isoforms, current methods fail to capture the entirety of APA chan

90 Furthermore, the limits of detection of the current method for A. baumannii M3237 and 54149 are ~10(

91 The current method for avoiding such sample mixups is to tes

92 utilizing an electrokinetic-based streaming current method for signal transduction is proposed.

93 However, current methods for analyzing diploid Hi-C data cannot f

94 Nevertheless, current methods for analyzing patterns that arise from c

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

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

97 ne interventions have raised questions about current methods for assessing environmental exposure to

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

99 decisions across agricultural landscapes but current methods for assessing these benefits may underes

100 Current methods for assigning cell types typically invol

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

102 Current methods for bacterial identification rely on gen

103 Most current methods for BCR sequence analysis focus on separ

104 Current methods for biochemical and biogeochemical analy

105 Current methods for bioprinting functional tissue lack a

106 the potential of the approach to complement current methods for classifying quality attributes in be

107 Current methods for CTC isolation and identification are

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

109 Current methods for detecting CNVs from exome-sequencing

110 Current methods for detection and diagnosis of allergies

111 Current methods for determining RNA structure with short

112 Current methods for diagnosing DMD are often laborious,

113 However, current methods for directly measuring regional pollen c

114 Current methods for discriminating lymphocyte cell types

115 Current methods for entropy estimation suffer from a hig

116 Current methods for enzymatic activity measurement often

117 Current methods for evaluating persistence are based on

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

119 Current methods for evaluation of antibacterial treatmen

120 Current methods for examining mechanical force generatio

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

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

123 However, current methods for fluorescent in situ detection of sRN

124 Current methods for gap filling either fall into the net

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

126 As current methods for identification of co-expression cann

127 Current methods for identifying azole resistance are tim

128 Current methods for imaging cellular metabolism are limi

129 cancer immunotherapy are summarized, and the current methods for imaging evaluations of immune-relate

130 Current methods for in vivo quantification of mutagenesi

131 Current methods for intraoperative histology are time- a

132 However, current methods for its isolation and characterization s

133 Current methods for liquid-liquid extractions generally

134 marking tests show that MUscADEL outperforms current methods for lysine PTM characterization, demonst

135 Current methods for magnetizing cells use artificial MNP

136 TCGI has dramatically improved the current methods for mapping genetic interactions and scr

137 However, current methods for measurement of ammonia are spectroph

138 Current methods for measuring gene expression in single

139 Current methods for measuring hydrogenase activity have

140 Current methods for measuring PT require regular visits

141 The current methods for monitoring GFD conformance, such as

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

143 Current methods for noninvasively imaging tumor perfusio

144 Most of the current methods for overcoming the diffraction limit in

145 Current methods for pathogen detection in the clinical l

146 ted peptides identified in recent years, the current methods for peptide database searching cannot ra

147 However, current methods for photon recuperation are limited by i

148 Current methods for predicting adverse events in patient

149 oal of the present review is to describe the current methods for preparing macroscopic composite film

150 Thus, our findings indicate that current methods for producing iPSCs are appropriate for

151 illustrate the unique advantages of MP over current methods for rapid sample characterization, prior

152 However, current methods for RBC analysis and MCHC quantification

153 In this study, we first reviewed current methods for scavenging capacity measurement to i

154 ologies can uncover biological insights, but current methods for scRNA-seq data integration are limit

155 However, current methods for segmenting nuclei in 3D tissues are

156 Current methods for sgRNA design are mainly concerned wi

157 Current methods for single-cell RNA sequencing (scRNA-se

158 However, the current methods for studying global DNA methylation leve

159 Current methods for studying lysine-based polyubiquitina

160 Current methods for Suzuki-Miyaura couplings of nontrifl

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

162 We close with a review of current methods for the analysis of data from these desi

163 Current methods for the detection of misfolded proteins

164 d can become an effective alternative to the current methods for the determination of the total hydro

165 Current methods for the quantification of different orga

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

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

168 However, current methods for their functional reconstitution in b

169 Current methods for tracking GPCR signaling suffer from

170 Current methods for transcript discovery rely on a '2-St

171 Current methods for treating combustion exhaust include

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

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

174 However, the current methods have certain limitations such as the req

175 ere is extensive work in this area, however, current methods have difficulty with one or more of the

176 burden in cancer, specifically in GBM, where current methods have largely failed.

177 Despite this interest, current methods have limitations: sampling unsuitable fo

178 The current methods have limited capabilities of continuous

179 Although current methods have mostly focused on analyzing bacteri

180 Current methods have not been evaluated for their abilit

181 Current methods have not yet satisfied the need for rapi

182 None of the current methods have supported the recovery of murine RV

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

184 imation of the mixture model and outperforms current methods in identifying differentially abundant f

185 Most current methods in single-cell analysis rely on cell man

186 The current methods in use suffer many limitations and need

187 Current methods integrate patient history, neuropsycholo

188 The utility of the current method is demonstrated by gram scale synthesis o

189 atic reactions with MS-based proteomics, the current method is highly effective to globally and site-

190 underdetected, which might indicate that the current method is less than optimal for analyzing this g

191 t the available embryo culture medium in the current method is only a few microlitres.

192 ion stoichiometries in mammalian cells using current methods is cumbersome, complex, or expensive.

193 However, the predictive performance of the current methods is modest.

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

195 Current methods lack high sensitivity to detect small tu

196 have the potential for early detection, but current methods lack sensitivity and/or are time-consumi

197 s at much lower sequencing coverage than the current methods, leading to ~ 80% lower sequencing cost

198 Current methods limit the biological contexts that can b

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

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

201 ll as improving on the speed and accuracy of current methods, new analysis tools are provided to clus

202 The current method of diagnosis relies on microbiological cu

203 The current method of synthesizing these hybrids via direct

204 e a critical discussion of the advantages of current methods of (bio)sensing of creatinine, as well a

205 We argue that current methods of behavioral parameterization are limit

206 ransmission of Vibrio cholerae in Haiti with current methods of control is low, and that bolder actio

207 Current methods of determining AMR rely on inefficient p

208 Current methods of estimating IFTA are slow, labor-inten

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

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

211 Current methods of identifying activated CD8(+) T cells

212 However, most current methods of inferring DGRNs from bulk samples may

213 aragraph of the subsection 'A perspective on current methods of ligand identification' was incorrect;

214 However, current methods of liquid sample introduction to a detec

215 Current methods of measuring these parameters in Drosoph

216 i.e., culling infected individuals), whereas current methods of molecular (qPCR) and visual detection

217 Current methods of MSC tracking include labelling the ce

218 Current methods of network comparison are limited to ext

219 1, addresses some of the challenges faced by current methods of nucleic acid-based assays and symptom

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 However, the current methods of preparation rely on mechanical mixing

223 rovides additional prognostic information to current methods of risk stratification.

224 However, the current methods of TIL analysis are subjective and open

225 Although current methods of treatment for cervical cancer can abl

226 In addition, current methods often favor common cell types, and miss

227 However, current methods often miss visually evident CTCF loops i

228 Current methods often report large numbers of motifs, ma

229 Compared with current methods on both simulated and experimental densi

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

231 Most current methods perform well on molecular function predi

232 Current methods present low ion selectivity, and require

233 The current method progresses upon multiple reaction monitor

234 Many current methods provide a single solution to this proble

235 Current methods quantifying the extent to which a suspen

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

237 Current methods rely on external imaging techniques or i

238 Most current methods rely on features that are manually selec

239 Current methods rely on retinal densitometry to distingu

240 Most of the current methods rely on the design of specialized coupli

241 titative analysis of histological images but current methods require application-specific algorithm t

242 Current methods require careful samples storage and hand

243 Current methods require lengthy reaction times or diffic

244 is approach presents several advantages over current methods.See related article by Ostmeyer et al.,

245 epts involved in computing genetic risk with current methods, strengths and weaknesses of various app

246 However, current methods suffer from interference between the sin

247 Unfortunately, current methods suffer from invasiveness, poor resolutio

248 Current methods target signature peptides resulting from

249 However, current methods to achieve this have specific requiremen

250 Current methods to achieve transition-metal-catalyzed al

251 Current methods to address this challenge are often depe

252 opathy disorders and provides an overview of current methods to assess protein misfolding and pathoge

253 Current methods to characterize gene expression mediatin

254 Current methods to correlate a cell's position with its

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

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

257 Current methods to detect aggregation of biological mole

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

259 Limitations of current methods to detect drought-induced xylem blockage

260 to investigate whether egg CRD could improve current methods to diagnose various egg allergy phenotyp

261 However, current methods to effectively deplete rRNA of diverse n

262 Current methods to estimate the cell type proportions in

263 However, current methods to form carbon-carbon bonds between hydr

264 However, current methods to generate hypomorphic mutations are li

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

266 Current methods to investigate neuraminidase activity us

267 However, current methods to measure cooperativity parameters have

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

269 Current methods to measure organism size, and in particu

270 Current methods to measure supracellular mechanical prop

271 Current methods to monitor and mitigate unhealthy ponds

272 Current methods to monitor neural activity, however, lac

273 Current methods to obtain such models rely on determinin

274 Current methods to optimize cluster labels and number ca

275 Current methods to prepare nanocrystal arrays lack the p

276 g, and quinary structure in the cell and the current methods to quantify them both in vitro and in vi

277 Current methods to reduce alloantibodies are only modest

278 Because current methods to study GTO circuitry (nerve stimulatio

279 distinct roles in cortical computation, but current methods to study them in humans are limited.

280 Current methods toward incorporating lithium in sulfur-s

281 However, current methods typically make the simplifying assumptio

282 Current methods typically use descriptors constructed fr

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

284 We share here the current methods used by Michigan Medicine to address the

285 Current methods used for CNT aerosol measurement lack se

286 Current methods used for confirmation of identification,

287 t importance that continues to challenge the current methods used in this area, whose difficulty is f

288 laborious nature and low sensitivity of the current methods used to assess transmission intensity.

289 Current methods used to characterize the mechanodynamics

290 esults provide important improvements to the current methods used to isolate circular RNAs as well as

291 This includes a review of current methods used to monitor intradialytic cerebral p

292 The current methods used to routinely assess freshness in th

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

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

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

296 By comparison to current methods, we show that FICC-Seq is a particularly

297 ming statistical inference compared to other current methods when missing values are due to a mixture

298 classified as "inactive" or are invisible to current methods which could become the next generation o

299 cy of AllerCatPro is 84% compared with other current methods which range from 51 to 73%.

300 itical to advance glycoscience research, the current method without any sample restrictions can be wi