ライフサイエンスコーパス: sample

1 99% 5-fold genome coverage (in 9/20 clinical samples).

2 lved with reference to a constant-emissivity sample.

3 esicles/mL, using as little as 60 muL of the sample.

4 nt B cell subpopulations present in a single sample.

5 n defined by each rule compared to the total sample.

6 r all three CT signatures in the replication sample.

7 Particle size was also measured for each sample.

8 and detection of HSIL at the margins of LEEP sample.

9 etect thousands of molecules in a biological sample.

10 onmental information where the networks were sampled.

11 tion of low pathogen concentrations in water samples.

12 viously went undetected in bulk brain tissue samples.

13 p loss and colour were evaluated with thawed samples.

14 eliminating the need for heating and shaking samples.

15 knowledge of compounds observed in superfood samples.

16 enetic polymorphism in human brain and heart samples.

17 outinely assessed in oriented (15) N-labeled samples.

18 olecule localization microscopy on live-cell samples.

19 ndings were consistently observed in the two samples.

20 E, compared to the control and other treated samples.

21 ions using archaic, ancient and modern human samples.

22 ce for assessing its origin in environmental samples.

23 zein gene from maize in eight cereal product samples.

24 nal PCR/sequencing of residual blood culture samples.

25 covery rate for the detection of SDS in real samples.

26 on events with variable incorporation across samples.

27 le for large-scale studies in primary tissue samples.

28 cluded 28 Parkinson's disease and 43 control samples.

29 d construct a test statistic based on finite samples.

30 ed settings, and with relatively homogeneous samples.

31 nificantly (p < 0.05) increased in FIR dried samples.

32 reek samples, and -26.1 to -24.5 for Iranian samples.

33 ype 4 (ST4) cysts, isolated from human stool samples.

34 ate esters in yogurt, water, and soybean oil samples.

35 ommended by international agencies in cereal samples.

36 bolic profiling of albedo, flavedo and juice samples.

37 s) in the pathogen genomes sourced from host samples.

38 l component analysis showed that for all six samples a very good discrimination based on the cultivar

39 endocarditis (IE) in the National Inpatient Sample, a representative sample of United States hospita

40 We utilized the 2016 National Inpatient Sample-a nationally representative database of all disch

41 stratified two-phase flow, consisting of the sampled air stream and a stream of collection medium, is

42 atch annotation of TCR repertoire sequencing samples allows for annotating large datasets on-line.

43 s were found in 0/20 blood vs. 11/20 aqueous samples along with shorter DNA fragments.

44 d that the enthalpies of the HMT and the CAT samples along with the onset, peak, and conclusion tempe

45 By sampling along the discriminant dimension, and back-proj

46 Our sample also shows robust correlations between individual

47 Among the 1249 samples analyzed, the alpha-diversity of the fecal micro

48 dem MS information for each component in the sample and correlates product ions to their correspondin

49 n and treatment resistance, peripheral blood samples and intestinal allograft biopsies from 51 ITx pa

50 s that can arise with the use of convenience samples and offer guidance for moving towards more repre

51 riven elements allow for the manipulation of samples and reagents with an unprecedented precision and

52 cing of ASH1L in additional 524 unrelated TS samples and replicated the association (P value = 0.001)

53 s research, especially when processing trace samples and where multiple measurements are desired.

54 be applicable to a wide range of biological samples and will help to improve the sensitivity of nucl

55 ize exploratory tools that can guide spatial sampling and highlight the need for greater use of mixed

56 ameter correlations by implementing adaptive sampling and stimulation protocols compatible with param

57 muL of sample in a fast (less than 1 min per sample) and high-throughput (up to 384 samples per run)

58 for all tested regions using the EEM of each sample, and overall 97.7% for ICP-MS.

59 c measurements were -28.3 to -26.9 for Greek samples, and -26.1 to -24.5 for Iranian samples.

60 vaginal samples, provider-collected cervical samples, and cervical biopsy samples were obtained from

61 genomic and/or proteomic analysis of patient samples, and phenotypic assays in personalized cancer av

62 rate ranged from 46.4% to 69.5% under biased sampling, and was equal to 75% for the unbiased scenario

63 n small areas based on enumeration data from sample areas and nationwide information about administra

64 .2, whereas it was the lowest in the control sample as 49.1.

65 We leveraged samples assembled over decades of fieldwork to study div

66 t and grade cancer in prostate needle biopsy samples at a ranking comparable to that of international

67 ical covariates in 134 neuroblastoma patient samples at diagnosis.

68 and had sparse dolutegravir pharmacokinetic sampling at weeks 8, 11, and 16.

69 y, targeting individuals in non-help-seeking samples based only on more severe symptom cutoff thresho

70 ter stopping ART), who provided serial blood samples before death and their bodies for rapid autopsy.

71 -seq analysis, especially when the groups of samples being compared had distinct global within-group

72 Properties of the biosensor, sample, buffer fluid and even the microfluidic channel c

73 termination of cobalamin and cobalt in kefir samples by high performance liquid chromatography-induct

74 that genomic assessment of non-dysplastic BE samples can identify patients at greatest risk of progre

75 es that using 3- to 15-month or 2- to 3-year samples can predict allergy status at age 4(+) years.

76 e measured in atmospheric vapor and particle samples collected at six sites in the Laurentian Great L

77 ymatic digestion of extracted RNA within the sample collection tube.

78 iew key applications of advanced methods for sampling complex free-energy landscapes at near nonergod

79 However, human brain sampling complexities limit the explanatory power of bra

80 The study sample consisted of 1,282 mother-child pairs participati

81 s and can misrepresent relative abundance of sample constituents.

82 s of three model compounds in a fast and low sample consumption (<1 mg) manner.

83 One quarter of all tumor samples contain somatic integrations of telomeric sequen

84 The milk samples contained genetic material from various bacteria

85 consistently detected amplification only in samples containing pork.

86 asured the signatures of several combination samples containing two or four different MNW types, and

87 ges, we determined how well the brain region samples could be discriminated from each other, visually

88 ffered by an average of around 5% from blood samples counted on a calibrated gamma-counter.

89 cimens, cell lysates, and mouse liver tissue samples, demonstrating its highly sensitive and specific

90 of more than 100 well-characterized clinical samples diagnosed and confirmed using a previously publi

91 the Primer-ID method have analyzed clinical samples directly.

92 d in solution and crucially, the crystalline samples display thermal stabilities in good agreement wi

93 We find that most SARS-CoV-2 infections sampled during this time derive from a single introducti

94 In sediment samples, ECl-OPEs and Enonchlorinated-OPEs had median co

95 A new tissue sample embedding and processing method is presented that

96 S-CoV-2 viral genomes from available patient samples enabled us to estimate that SARS-CoV-2 was intro

97 The 128 water samples exhibited a high diversity of chemical and effec

98 The Im 3 m phase of D(3) S samples exhibits a T(c) significantly higher than previo

99 erferometric detection of absorption-induced sample expansion.

100 T cells were sampled for up to 11 weeks to capture steady-state and p

101 ing extended molecular dynamics and enhanced sampling free-energy simulations, we observed that the c

102 ha-1 antitrypsin concentrations.Methods: DNA samples from 1,693 non-Hispanic white individuals, 385 A

103 easured by using Luminex technology in serum samples from 146 patients with severe AD (median Eczema

104 We obtained blood samples from 185 young women (average age 21.2) in two c

105 bosomal RNA analyses were performed on stool samples from 405 HIV-infected and 111 uninfected partici

106 Tissue microarray (TMA) samples from 415 tissues collected from three cancer cen

107 takes 5 d to complete, and can be applied to samples from any organism, as long as a sufficient amoun

108 ship with a central laboratory that receives samples from approximately 1300 dialysis facilities acro

109 at autopsy were present in tissue and blood samples from earlier time points.

110 Twenty-nine samples from individuals with no evidence of TB infectio

111 PV samples from IRI+ orthotopic liver transplantation (OLT)

112 ols (PI) were also detected in the BM plasma samples from MM compared to MGUS patients.

113 NA sequencing metagenomics(4-6) of placental samples from normal and complicated pregnancies.

114 Whole blood samples from patients treated for symptomatic CAD includ

115 vely imaged PD-1/PD-L1 interactions in tumor samples from patients, employing an assay that readily d

116 Reduction in neuroinflammation by using samples from post-FMT patients to colonize GF mice shows

117 pathogen peptides were identified in 40% of samples from PTLDS and TBI patients (categories 2 and 3

118 her evaluated with a large cohort of blinded samples from the CDC and Columbia University.

119 In RNA-Seq analyses of human brain samples from the NYGC ALS cohort, truncated STMN2 RNA wa

120 Eighty-seven flour samples from two rice kinds (Indica and Japonica) plus t

121 We propose a sequential approach to sampling from the joint features population distribution

122 blind clinical evaluations of 100 suspected samples furtherly confirmed the superior sensitivity/spe

123 ectrometry (MALDI-TOF MS) with only 1 muL of sample in a fast (less than 1 min per sample) and high-t

124 RT-PCR testing of cerebrospinal fluid (CSF) samples in children impacted care of hospitalized neonat

125 Extraction methods for samples in microfluidic systems have been limited as thi

126 tabolic profiles of hundreds to thousands of samples in the Cancer Genome Atlas (TCGA).

127 The final sample included 284 544 physicians (76.1% men, 60.1% wit

128 Participants in the initial sample included 840 trauma-exposed individuals recruited

129 data sets from primates using frozen tissue samples, including many data sets from our own group, we

130 elanin granules as compared to the untreated sample, indicating the degradation of melanin.

131 Most were consistent across samples, indicating that they are part of a core mycobio

132 survival and reproductive success across all sampled individuals.

133 ccidental, young children (4 or 5 y) in this sample inferred the nonaccidental structure was socializ

134 ach separation and quantifying the amount of sample injected onto the capillary.

135 ionization mass spectrometry (ESI-MS)-based sample injection at a sampling rate faster than current

136 We divided the sample into a training and a testing set and used machin

137 oronavirus 2 (SARS-CoV-2) RNA in respiratory samples is the standard method for diagnosis.

138 NADH) and vitamin A were scanned on sturgeon samples kept at 4 degrees C up to 12 days.

139 A sample-to-sample matrix revealed that MPS populations could be sep

140 f a metabolic feature calculated between two samples may not reflect their real metabolic concentrati

141 For culture-negative samples, mean cost-per-positive 16S PCR result was pound

142 In total, 1,710 samples met inclusion criteria.

143 n peer-reviewed journals; used probabilistic sampling methods and systematic PTSD assessments; and in

144 y based on LAMP, in a closed tube, undiluted sample molecular diagnostic.

145 licit solvent simulations, were employed for sampling multiple cycles of LIV-BPSS clamshell-like conf

146 em brain (n = 206) and 1 collection of blood samples (N = 1132) of MDD cases and controls, we used ep

147 (n = 31), CSFs (n = 11), longitudinal serum samples (n = 15), and using mAbs (n = 14) generated from

148 g in both brain (n = 109) and matching serum samples (n = 566) to identify differentially expressed m

149 (TMS) for treatment of depression (discovery sample, N=30; active replication sample, N=81; sham repl

150 (discovery sample, N=30; active replication sample, N=81; sham replication sample, N=87).

151 e replication sample, N=81; sham replication sample, N=87).

152 With the most performing sample (Na/Ca_0.27), a comprehensive study on simultaneo

153 th maximal value of 52% for the conventional sample obtained at pH9, whereas the maximal FC of 28% wa

154 f 28% was observed for the electro-activated sample obtained by using Anolyte_450mA-50 min.

155 We analyzed metal levels in erythrocyte samples obtained at recruitment, as a biomarker for meta

156 Non-centrifugal cane sugar (NCS) samples obtained by traditional moulding and granulation

157 ed prospectively on 10,240 CTCs in 367 blood samples obtained from 294 patients with progressing meta

158 studies performed on human beta-cells or on samples obtained from patients with diabetes mellitus.

159 Construct validity was evaluated on a sample of 120 patients who underwent laparoscopic Roux-e

160 s in an extensively phenotyped developmental sample of 345 participants (312 healthy and 33 with clin

161 In the test sample of 49 gliomas (nine IDH wild type, 21 IDH mutant/

162 e was associated with EVALI in a convenience sample of 51 patients in 16 states across the United Sta

163 al self-harm (NSSH) in an independent target sample of 8,703 Australian adults.

164 In a large sample of community-dwelling individuals, acute exercise

165 in only 4.5-6 h using only 3 muL of bacteria sample of each reaction (as opposed to 24 h and 50 muL,

166 arbohydrate profile of GWA honeydew honey, a sample of GWA honeydew honey was found to contain 37.8%

167 l types or developmental trajectories in the sample of interest.

168 observed a low HCV prevalence in this large sample of MSM despite a high prevalence of known risk fa

169 e, we applied neuroimaging in a longitudinal sample of n = 146 participants aged 12-30.

170 National Inpatient Sample, a representative sample of United States hospitalizations from January 20

171 N, SETTING, AND PARTICIPANTS: Representative sample of US adults aged at least 40 years in the Nation

172 spike protein, and subsequently tested with samples of anti-SARS-CoV-2 monoclonal antibody CR3022 (0

173 Two different representative samples of children aged 6-29 months and their mothers w

174 using HEK293T, Panc-1, and Panc-28 cells and samples of human pancreatic intraepithelial neoplasia (P

175 IgA-Biome) was conducted on stool and saliva samples of normoglycemic participants and individuals wi

176 re microbial communities from EDC and sputum samples of patients according to type 2 (T2)-asthma endo

177 gene down-regulation in postmortem cortical samples of patients with depression.

178 ssociation was replicated in two independent samples of SJLIFE survivors of European ancestry, includ

179 ctive site structure and specificity among a sampling of plant pathogen Cdc14 homologs.

180 On the other hand, sampling of protonation states only leads to good result

181 Modern recording methods enable sampling of thousands of neurons during the performance

182 ge is more apparent in datasets with limited samples or unbalanced group proportions.

183 tection mechanism allows continuous stimulus sampling over a wide dynamic range.

184 We showed that multiple histological samples per patient is necessary to effectively capture

185 n per sample) and high-throughput (up to 384 samples per run) way.

186 two days per week, throughout an eight-week sampling period during influenza season.

187 or approximately 68 t was calculated for the sampling period from February 2018 to January 2019.

188 a disturbance score was calculated for each sampling period.

189 In our randomly sampled population, CIN was more prevalent in domestic c

190 Sampled populations were classified according to income,

191 Respiratory samples positive for InfA that were collected at the sam

192 orm that included continuous water sampling, sample preparation (extraction), and analysis for the de

193 Improper sample preparation leads to detrimental cascades, result

194 ddress this bottleneck, we combine automated sample preparation, an ultra-fast 84-second LC-MS method

195 The samples pretreated by microwave have registered higher p

196 ce per year during a narrow temporal window, sample processing is a time-limiting step for research o

197 Meta-analyses of one-sample proportions were done in all patients receiving C

198 arriving at a classification of a MALDI-ToF sample, provided the collagen sequences for each candida

199 Urine samples, self-collected cervicovaginal samples, provider-collected cervical samples, and cervic

200 ned to overcome the inevitable variations in sample quality resulting from uncontrollable factors in

201 s were detected in individual aquatic insect samples (range of <limit of detection [<LOD] to 1670.10

202 rometry (ESI-MS)-based sample injection at a sampling rate faster than current ESI and matrix-assiste

203 ssation of discharging hypersaline brine, we sampled reef fishes at two outlet sites and two close re

204 A benchmark test based on the murine brain samples revealed a highly improved annotation quality as

205 In cancer patient samples, RITA, AF, and Onc-1 sensitized to poly(ADP-ribo

206 ical platform that included continuous water sampling, sample preparation (extraction), and analysis

207 idelines should include specific guidance on sampling schemes.

208 Urine samples, self-collected cervicovaginal samples, provider

209 However, an adequate sample size as a statistical necessity for radiomics stu

210 Two-arm RCTs were reviewed to see if sample size estimation was mentioned in the text and if

211 72 vs. 148) and 25% (36 vs. 142) of original sample size for MAIC of benralizumab vs. mepolizumab and

212 Effective sample size was 49% (72 vs. 148) and 25% (36 vs. 142) of

213 Post hoc analysis, small sample size, and examination of only patients with 1-yea

214 se of its restricted geographic scope, small sample size, and possible recall bias, which are typical

215 power for this was low because of the small sample size.

216 de more power and thus may require a smaller sample size.

217 nded by indications for surgery or has small sample size.

218 Here we explore power and sample-size calculations to evaluate potential correlate

219 eatment effect estimation, (3) volatility in sample-size distributions that can cause a nontrivial pr

220 modate general environment variables, modest sample sizes, heterogeneous noise, and binary traits.

221 el-based experimental probes; recruit larger sample sizes; and use single case experimental designs f

222 -selective electrodes immersed into separate sample solutions of equal composition.

223 metric box was designed to capture images of sample solutions.

224 ptance limit for consumption of chicken meat samples stored at 4 degrees C, 15 degrees C and 25 degre

225 an be reliably created and freely moved on a sample substrate.

226 f such methods to broadly available clinical samples such as formalin-fixed and paraffin-embedded (FF

227 ential migrants from plastics in challenging samples such as honey.

228 used metabarcoding data coupled with in situ sampling/survey data to explore the relative importance

229 d recovery experiments after spiking in food samples (Tea, coffee, chocolate, spinach, infant milk su

230 mark the performance of CV19-Net, a randomly sampled test data set composed of 500 chest radiographs

231 Of the 1494 samples tested from first-time male donors, 9 (0.6%; 95%

232 In out-of-sample tests on manually replicated papers from diverse

233 complex, was more abundant from bronchoscopy samples than sputum, and differentially more abundant in

234 Importantly, this included 20 samples that required 30-39 threshold cycles of RT-qPCR

235 performed genetic assays on 5 years of field samples that showed persistent but highly variable frequ

236 ted from some lung, brain, liver, and kidney samples that were ZsG and/or PCR positive, and only from

237 In 4 of the 141 clinical samples, the BCID-FP panel correctly identified an addit

238 While in tomato and potato samples, the maximum concentrations of ETU residues were

239 erved higher sensitivities with the Omniswab samples, this appeared to be due primarily to difference

240 cer cell-lines and two patient tumour tissue samples through a qPCR instrument and finally piloted on

241 ow for dramatically increased volumetric and sample throughput.

242 c slide loader automates 3D imaging for high sample-throughput.

243 eting more diverse populations and prolonged sampling times are required.

244 We subjected these samples to exon-level analysis with rMATS-turbo, purpose

245 methods can be parallelized across multiple samples to increase throughput.

246 cle detachment model and environmental field sampling to estimate the role of land cover change and s

247 A sample-to-sample matrix revealed that MPS populations co

248 iscovery of acesulfame and PFAS in most OSPW samples, trace levels in groundwaters influenced by gene

249 ffer was developed to minimize the number of sample-transfer steps and facilitate the direct enzymati

250 Moreover, the method does not require sample treatment or washing steps.

251 as performed on 20 matched blood and aqueous samples; tumor-associated chromosomal changes were found

252 that allow for the rapid collection of vapor samples under thermodynamic conditions are (1) the use o

253 regarding the local structure of ball-milled samples, underlining the sodium disorder and showing tha

254 hes since the kidney biopsy, blood and urine samples used to generate these different types of molecu

255 The AEMS platform achieved a speed of 2.2 s/sample using only 10 nL of sample volume.

256 ime POC device to detect SARS-CoV-2 from VTM samples using an additively manufactured three-dimension

257 identify and quantify Sudan I dye in ketchup samples using colour histograms (obtained from digital i

258 nomic sequencing data obtained from clinical samples using R9.4.1 Nanopore sequencing.

259 veal time profiles of dissolved O(2) in each sample vial, from which Threshold Time of sensor signal

260 e of parameters name as pH, extraction time, sample volume and amount of sorbent were optimized using

261 a speed of 2.2 s/sample using only 10 nL of sample volume.

262 19 and October 27, 2016, a systematic random sample was assessed for eligibility (HIV+, age >= 14 yea

263 d polyamine oxidase (PAO) activities in milk samples was developed.

264 ation of the method on various environmental samples was investigated to examine its capacity to prov

265 Farming-system authentication on cheese samples was less efficient than on milk, but still possi

266 In a separate sample, we investigated the neuronal gene expression ass

267 Using representative samples, we find that person-country and person-region v

268 nce in the country, adjusted for cluster and sample weight.

269 imates across population subsets relative to sample weighting, and there was some evidence of small g

270 ts was offset by the CO(2) mineralised (i.e. samples were 'carbon negative', even when 10% w/w CEM 1

271 ns (RSD) between the cycles for human plasma samples were 0.84-6.6%.

272 sitivities in female vaginal swabs and urine samples were 96.6% (95% confidence interval [CI], 88.5 t

273 Saliva and serum samples were also collected.

274 and Japonica) plus thirty adulterated flour samples were analyzed by ICP OES.

275 uring a 20-day experimental period and blood samples were collected for hemogram determination and pe

276 Blood and urine samples were collected for up to 4 h after injection to

277 Colostrum and early lactation milk samples were collected from 285 mothers enrolled in a hi

278 Samples were collected from 550 participants (298 cases

279 a full periodontal clinical assessment, GCF samples were collected from healthy (n = 5) and diseased

280 Air samples were collected from multiple locations in the sc

281 Air and surface samples were collected from seven clinical areas, occupi

282 k of spatial resolution as either the tissue samples were homogenized or specific proteins were selec

283 GCF samples were investigated by means of fluorescent in sit

284 Overall, 636 (22%) samples were norovirus-positive, of which 567 (89%) were

285 Clinical data and biological samples were obtained at admission, days 3 to 5, and day

286 Skin and blood samples were obtained from 61 patients with AD (20 with

287 lected cervical samples, and cervical biopsy samples were obtained from all enrolled women.

288 Corneal samples were obtained from human donors with and without

289 Correlative studies on blood and tumor samples were performed to investigate potential biomarke

290 Random samples were selected from the lists of the California B

291 ination of the two mycotoxins in whole grain samples (wheat and maize).

292 irmed by analyzing the Ni-spiked compact COx samples, whereby an increase of the Ni content in the cl

293 odes (SPCE) suitable for analyses in gaseous samples which are of course lacking in supporting electr

294 nd instead can only be inferred from genetic samples, which are unavoidably subject to measurement er

295 dies follow a longitudinal design to collect samples, which further complicates the analysis methods

296 n effectively distinguish tumors from normal samples with an accuracy of 90% for Pan-Cancer and reach

297 pounds previously identified in human plasma samples with annotations generated by three similar tool

298 Samples with low immune infiltrate had higher number of

299 ating hematocrit (Hct) values of whole blood samples with nominal content of 28%, 35%, 40%, and 45% H

300 We find that CS-Rosetta sampling with unsigned chemical shift changes generates