ライフサイエンスコーパス: genomic analysis

1 c conditions, which was further supported by genomic analysis.

2 om the past, present, or future, followed by genomic analysis.

3 ome coverage (0.21x to 3.93x) for population genomic analysis.

4 24 (88%) of these had isolates available for genomic analysis.

5 All biopsy specimens had adequate yields for genomic analysis.

6 or properties can be highly complementary to genomic analysis.

7 numerous sequences simultaneously, prior to genomic analysis.

8 erum and identified by mass spectrometry and genomic analysis.

9 e often higher, which impacts the downstream genomic analysis.

10 as surprisingly emerged from biochemical and genomic analysis.

11 mapping with those from DNA sequencing-based genomic analysis.

12 ly 1% D. mccartyi cells successfully enabled genomic analysis.

13 sis for follow-up replication and functional genomic analysis.

14 DEPArray NxT system, followed by downstream genomic analysis.

15 nterval-based comparisons are fundamental to genomic analysis.

16 ing demand for cloud-computing solutions for genomics analysis.

17 F-seq and used them to perform a comparative genomics analysis.

18 ty induced by condition change in functional genomics analysis.

19 nd PAH lung pericytes followed by functional genomics analysis.

20 ach related organism used in the comparative genomics analysis.

21 e world, lends itself ideally to single-cell genomics analysis.

22 re, compared with 64 patients (63%) based on genomic analysis (73% VREfm).

23 have opened opportunities for droplet-based genomic analysis(9) but this approach has not yet been a

24 In order to facilitate genomic analysis, a fluorescence-activated cell sorting

25 While bulk tissue genomic analysis across large populations of tumour cell

26 Conclusion: Genomic analysis across the different stages of HCC reve

27 mutations that may have been missed through genomic analysis alone.

28 information that cannot be discerned through genomic analysis alone.

29 SL precursor RNA (slRNA; 108-158 nt) through genomic analysis and 3'-RACE technique, which was confir

30 Our extensive genomic analysis and comparisons with non-raptor genomes

31 Genomic analysis and deep RNA-Seq across infection time

32 Genomic analysis and epidemiologic data were used to ide

33 structure and replicative cycle, along with genomic analysis and genomic comparisons with previously

34 egrated Set Profile Analysis) for integrated genomic analysis and its variation, SISPA (Sample Integr

35 In summary, integration of genomic analysis and microRNA expression profiling could

36 Concurrent advances in tumor genomic analysis and molecular inhibitor development hav

37 Five clades, determined by genomic analysis and named by the distinct regions where

38 for distribution of specimens to pathology, genomic analysis and PDX/cell line creation facilities;

39 Through comparative genomic analysis and ribosome profiling we here identify

40 ect genetic modification for both functional genomic analysis and the control of insect populations.

41 n neuroblastoma patient tumors using the R2: Genomics Analysis and Visualization Platform revealed th

42 While restriction enzymes have advanced genomic analysis, and trypsin has advanced proteomic ana

43 We employed a comparative genomic analysis approach using the 28 isolates comprisi

44 e performed a comparative transcriptomic and genomic analysis at the level of one single plant cell t

45 EY MESSAGE: A comparative transcriptomic and genomic analysis between Arabidopsis thaliana and Glycin

46 Here we apply comparative functional genomic analysis between C. elegans and Caenorhabditis b

47 We hypothesize that genomic analysis between pre-invasive and invasive compo

48 Comparative genomic analysis between tambaqui and zebrafish revealed

49 h new advances in gene editing, imaging, and genomic analysis, brain organoid technology can be appli

50 Genomic analysis by massively parallel sequencing of 504

51 ics and systems biology approaches including genomic analysis, coevolution and network-based modeling

52 Proteomics and genomics analysis corroborated that WSUCF1 biofilms uses

53 Genomic analysis coupled with proteomic validation revea

54 allow for rapid and inexpensive large-scale genomic analysis, creating unprecedented opportunities t

55 Comparative genomic analysis demonstrated that the type III secreted

56 A combined immuno-genomic analysis demonstrated the immune microenvironmen

57 XD2A-HTRA1 fusion in 12/125 (10%) cases, and genomic analysis demonstrated the mechanism as resulting

58 Morphological and genomic analysis determined that it was a new species, d

59 Herein, comparative genomic analysis divided hpEurope into two groups: hpEur

60 sequencing data has improved the results of genomic analysis due to the resolution of mapping algori

61 ulti-scale insight across multiple layers of genomic analysis (e.g., differential expression analysis

62 ion dynamic modelling and CML patient biopsy genomic analysis enables patient stratification at unpre

63 d the power of family-based, population-wide genomic analysis for gene and mutation discovery.

64 ur study highlights the power of comparative genomic analysis for identifying species and populations

65 irected acyclic graphs (DAGs) in a genetical genomics analysis framework.

66 Our genomic analysis has also revealed that DSBR at the lacZ

67 The computer software used for genomic analysis has become a crucial component of the i

68 Genomic analysis has connected altered astrocytic gene e

69 Genomic analysis has greatly influenced the diagnosis an

70 Single-cell genomic analysis has grown rapidly in recent years and f

71 Genomic analysis has identified that genes required for

72 Comparative genomic analysis has led to the discovery of a new class

73 Comprehensive genomic analysis has revealed a list of molecular aberra

74 Recent genomic analysis has shown that many of the most commonl

75 However, preliminary genomic analysis has suggested that genome-guided approa

76 ncer immunotherapies, along with advances in genomic analysis, has led to the identification of tumor

77 In summary, our functional genomics analysis highlighted novel genes and critical p

78 Cancer genomic analysis identified frequent amplification of US

79 Comparative genomic analysis identified genes that were unique to ea

80 Here, integrative genomic analysis identified MYST3 as a potential oncogen

81 Genomic analysis identified selection for changes in mot

82 Our comparative genomic analysis identifies chromosome-level syntenic re

83 Here our integrative genomic analysis identifies tousled-like kinase 2 (TLK2)

84 A targeted genomic analysis implicated FOXM1 signaling downstream o

85 individual cells for whole-transcriptome or genomic analysis in a massively parallel manner with min

86 Trait mapping and integrative functional genomic analysis in GeneWeaver has allowed us to implica

87 tion of conditional mutations for functional genomic analysis in insects, and other organisms.

88 GenomeVIP has been used for genomic analysis in large-data projects such as the TCGA

89 that evolutionary inference from integrated genomic analysis in multisector biopsies can inform targ

90 of this study was to perform a comprehensive genomic analysis in order to unravel the genomic archite

91 ied informatic ecosystem to support pathogen genomic analysis in public-health agencies across income

92 We performed an integrative genomic analysis, incorporating whole exome sequencing (

93 Population genomic analysis indicated a recent colonization ( appro

94 ding proteins CheV and CheW, and comparative genomic analysis indicates a likely recent evolutionary

95 This principle applies more broadly since genomic analysis indicates suboptimal canonical miRNAs a

96 Genomic analysis indicates that the R330fs mutant can di

97 Genomic analysis indicates that this pathway is conserve

98 Genomic analysis is a powerful tool for understanding vi

99 important role in defining these conditions, genomic analysis is providing a platform for better dise

100 ISTA antibody in combination therapy and how genomic analysis may assist in providing indications for

101 datasets combining the output from multiple genomic analysis methods in an intuitive and interactive

102 Using genomic analysis, microscopy, and molecular perturbation

103 s demonstrate that pharmacotherapy guided by genomic analysis, molecular modeling, and functional pro

104 ed amplified polymorphic sequence analysis), genomic (analysis of variants) and cytogenetic (fluoresc

105 in R/M tumors is needed.METHODSAn integrated genomic analysis of 1,045 ACCs (177 primary, 868 R/M) wa

106 Through genomic analysis of 1,122 EGFR-mutant lung cancer cell-f

107 Using integrated genomic analysis of 1,988 childhood and adult cases, we

108 Through comparative genomic analysis of 12 Thermoplasmata metagenome-assembl

109 Here we present a comprehensive genomic analysis of 122 Saccharomyces hybrids and introg

110 Comparative genomic analysis of 129 and C57BL/6J mouse strains revea

111 We describe a genomic analysis of 1345 GBS isolates from neonatal (age

112 Genomic analysis of 18 emm1 isolates from Hong Kong and

113 Here, through combined epidemiological and genomic analysis of 2,186N.

114 Here we report genomic analysis of 2,693 samples collected post mortem

115 rify the genomic basis of CTCL, we performed genomic analysis of 220 CTCLs.

116 Here, I present a comparative genomic analysis of 250 MGII genomes, providing a compre

117 Using integrated genomic analysis of 264 T-ALL cases, we identified 106 p

118 Here we present a multiplatform genomic analysis of 37 patients with Sezary syndrome tha

119 Integrated genomic analysis of 456 pancreatic ductal adenocarcinoma

120 We present the genomic analysis of 75 samples from 57 representative pa

121 Lastly, population genomic analysis of 78 circum-basmati varieties shows th

122 In a genomic analysis of 78 FLC samples, we identified 3 clas

123 Through large-scale genomic analysis of 906 strains, we demonstrate that the

124 udinal study provides a unique comprehensive genomic analysis of a clonal lineage within a single ind

125 We performed genomic analysis of a congenital pigment synthesizing me

126 The present study represents an in-depth genomic analysis of a Pan African set of individuals, wh

127 that precision medicine approaches based on genomic analysis of a single specimen are likely insuffi

128 While genomic analysis of a small number of isolates has provi

129 This study provides a comprehensive genomic analysis of A. actinomycetemcomitans and the clo

130 High-resolution structural and functional genomic analysis of adult Burkitt lymphoma (BL) and high

131 f HGSCs, we report a multi-center integrated genomic analysis of advanced stage tumors with and witho

132 , population genetic analysis and functional genomic analysis of allelic activity.

133 nitiative, the most comprehensive up-to-date genomic analysis of any Latin-American population.

134 We present the first genomic analysis of Atro using ChIP-seq against endogeno

135 Genomic analysis of barley paints a picture of diffuse o

136 Genomic analysis of BQ11 identified acquisition of a nov

137 We performed an integrative genomic analysis of brain tissue-derived transcriptomes

138 also discuss connections revealed by recent genomic analysis of cancers between chromothripsis, chro

139 Genomic analysis of chromothripsis and the search for it

140 ot feasible for all patients and, therefore, genomic analysis of circulating tumour DNA (ctDNA) has e

141 Through genomic analysis of colorectal cancers and cell lines, w

142 on, here we perform integrated cross-species genomic analysis of cuSCC development through the preneo

143 These findings demonstrate that integrative genomic analysis of dietary information may reveal molec

144 In this study, we utilized integrated genomic analysis of DNA methylation, chromatin accessibi

145 Genomic analysis of drug response can provide unique ins

146 e describe an integrated epidemiological and genomic analysis of E. faecium associated with bloodstre

147 Genomic analysis of FFPET from the 4 phenotype-positive/

148 identify H. haemolyticus Through comparative genomic analysis of H. haemolyticus and NT H. influenzae

149 Our systematic genomic analysis of HAMPs across a large-scale cancer sp

150 ch allow the first comprehensive comparative genomic analysis of hepadnaviruses from four classes of

151 gh sensitivity of the algorithm also enables genomic analysis of heterogeneous pathogen genomes from

152 knowledge, our study represents the earliest genomic analysis of HIV-1 in the FGT after transmission.

153 en followed by comparison against functional genomic analysis of human and rodent beta cells exposed

154 Large-scale genomic analysis of human cancers indicates that the los

155 A recent integrative genomic analysis of human prostate cancers (PCas) has re

156 We performed genomic analysis of intrinsic and acquired resistance to

157 Genomic analysis of longevity offers the potential to il

158 Bioinformatic and genomic analysis of LOS biosynthetic genes indicated sig

159 Integrative genomic analysis of lung carcinoids identifies three nov

160 iven by TET deficiency (Tet2/3 DKO T cells), genomic analysis of malignant T cells revealed DNA hypom

161 this malignancy, we performed a large-scale genomic analysis of MCL using data from 51 exomes and 34

162 Comparative genomic analysis of mouse L-R mammary gene expression pr

163 Genomic analysis of mouse neoplasms induced by the Dnajb

164 ous cell carcinoma (OSCC), we have performed genomic analysis of mouse tongue lesions.

165 and inform treatment decisions.Significance: Genomic analysis of multiple individual cells harvested

166 Genomic analysis of Nbn (-/mid8vav) malignancies showed

167 We performed genomic analysis of new and published data from 249 PLGG

168 Here we report comparative genomic analysis of nine isogenic iPSC lines generated u

169 Genomic analysis of our cohort further identified mutati

170 Genomic analysis of paired tumor-normal samples and clin

171 In summary, by coupling the systematic genomic analysis of purified cancer cells in distinct ma

172 However, genomic analysis of recent EPEC isolates has revealed th

173 Longitudinal genomic analysis of rheumatoid arthritis flares revealed

174 To date, comprehensive genomic analysis of SBA is lacking.

175 Genomic analysis of sequence variants associated with an

176 Additional genomic analysis of sex chromosomes and sex-determining

177 Genomic analysis of Streptococcus thermophilus revealed

178 he authors conducted the first comprehensive genomic analysis of suicide death using previously unpub

179 A recent genomic analysis of Synechococcus cyanophages sampled fo

180 Comparative genomic analysis of the accessory genome of the extant S

181 Although high homology complicates genomic analysis of the ATAD3 defects, they can be ident

182 The infection's source was uncertain until genomic analysis of the fungal isolate identified its or

183 Integrative genomic analysis of the human AD brain transcriptome hol

184 re, we present an expansive phylogenetic and genomic analysis of the Trim5 cluster in rodents.

185 administered to the patient, and comparative genomic analysis of the various intestinal E. coli strai

186 We performed comparative genomic analysis of their source loci (PHAS) in five Ory

187 Genomic analysis of these EV-D68 strains revealed dynami

188 Genomic analysis of these mutants revealed a central rol

189 Comparative genomic analysis of this group, which we name Candidatus

190 Genomic analysis of this strain (NHDP-385) identified a

191 Genomic analysis of this strain (NHDP-385) identified a

192 Genomic analysis of this strain provided valuable inform

193 Genomic analysis of Treg cells by RNA-sequencing, Foxp3

194 responses to therapy have been identified by genomic analysis of tumor biopsies from individual patie

195 Genomic analysis of tumor biopsies revealed that vismode

196 They also have a strong influence on the genomic analysis of tumour samples, and may alter the bi

197 Genomic analysis of tumours has led to the identificatio

198 In contrast, genomic analysis of urine enriched by centrifugation dis

199 Genomic analysis of WFBV revealed that it is most closel

200 We then conducted a comprehensive genomic analysis of Y chromosome, mitochondrial DNA, and

201 Genomics analysis of a historically intriguing and predi

202 re-based virtual screening with the chemical genomics analysis of drug molecular signatures, and iden

203 Here we performed a systematic comparative genomics analysis of human disease-causing missense vari

204 We employed an integrative genomics analysis of master TFs CREB1 and FoxA1 in andro

205 Orthogonal genomics analysis of reprogrammed regulatory regions ide

206 The comparative genomics analysis of strain ZYK(T) implies that it share

207 Population genomics analysis of T. sinense reveals its genetic dive

208 for both small- and large-scale comparative genomics analysis of tRNA sequence features.

209 By means of a comprehensive genomic analysis on 6637 tissues of 21 tumor types, we h

210 al cells from complex samples for subsequent genomic analysis or cultivation is still in its early in

211 ollo to be integrated into multiple existing genomic analysis pipelines and heterogeneous laboratory

212 Variants identified by current genomic analysis pipelines contain many incorrectly call

213 Combined with epidemiologic data, the genomic analysis provides evidence of sexual transmissio

214 Our cross-species comparative genomic analysis provides unique insights into glioma et

215 ations, biochemical pathways and comparative genomic analysis results such as synteny blocks and homo

216 Genomic analysis revealed adaptations to oxygen-limitati

217 Genomic analysis revealed bi-allelic loss-of-function va

218 Genomic analysis revealed concentration-dependent action

219 Genomic analysis revealed degradation events in importan

220 Genomic analysis revealed genetic relatedness.

221 Genomic analysis revealed high rates of aneuploidy in he

222 Genomic analysis revealed that APT6V1A copy number is ga

223 Pan genomic analysis revealed that BREX and BREX-like system

224 Here, genomic analysis revealed that cultivated Z. latifolia h

225 n at the profibrotic genes, ACTA2 and COL1A1 Genomic analysis revealed that EP300 is highly enriched

226 ata support a co-factorial relationship, but genomic analysis revealed that Gli3 and Hand2 were enric

227 Comparative genomic analysis revealed that many of the bacterial and

228 m environment in both treatments, population genomic analysis revealed that phages altered both the t

229 creatic ductal adenocarcinoma (PDAC) and our genomic analysis revealed that SERPINB2 is frequently de

230 Genomic analysis revealed that the isolate lacked known

231 Genomic analysis revealed that the virus was phylogeneti

232 Genomic analysis revealed that these virulence-related g

233 Genomic analysis revealed that, in both parasitic and mu

234 Detailed genomic analysis revealed the presence of gene homologs

235 Genomics analysis revealed that all 8 isolates belonged

236 Single-cell genomic analysis reveals characteristic SCLC genomic cha

237 Comparative genomic analysis reveals that all serovars encode a subs

238 Moreover, comparative genomics analysis reveals that a greater number of activ

239 According to genomic analysis, S. suis is divided into asymptomatic c

240 Next, we used a novel in silico genomic analysis, searchable platform-independent expres

241 Genomic analysis showed substantial functional diversity

242 Genomic analysis showed that DSS3Phi8 is most closely re

243 In contrast, population genomic analysis showed that genetic differentiation bet

244 Our comparative genomic analysis showed that important cheese ripening e

245 Genomic analysis showed that most tumors spontaneously a

246 Genomic analysis showed that the swine and human isolate

247 Most importantly, a thorough genomic analysis showed that the variants were generally

248 Genomic analysis showed that they contain a three-domain

249 Comparative genomic analysis showed that two NOG1 copies are present

250 Genomic analysis showed that VTs were more likely than N

251 Population genomic analysis shows a population bottleneck in this s

252 oni, and Sphingopyxis alaskensis Comparative genomic analysis shows that, in Enterobacteriaceae, the

253 ramework for the assessment of computational genomics analysis skills, which includes standard operat

254 Genomic analysis strongly suggests EBOV transmission to

255 This sharing enables certain types of genomic analysis, such as identifying sample overlaps an

256 outinely used to obtain tissue for molecular genomic analysis; such analysis helps determine the diag

257 Genomic analysis suggested multiple introductions of the

258 has two inorganic phosphate (Pi) importers, genomic analysis suggested that S. aureus possesses thre

259 phosphosites are not readily explainable by genomic analysis, suggesting that druggable translationa

260 Our genomic analysis suggests replicative mechanisms as a pr

261 Genomic analysis suggests that DSS3Phi8 is a highly mosa

262 Genetic and genomic analysis suggests that H69 cleavage leads to the

263 Comparative genomic analysis suggests that some of these neurogenomi

264 Our genomic analysis suggests that the redox potential effec

265 Genomic analysis suggests the existence of two highly di

266 In contrast, genomic analysis supported spread of USA500 strains with

267 In contrast, genomic analysis supported spread of USA500 strains with

268 led clinical characterization and a complete genomic analysis that consisted of a combination of high

269 in order to address inequalities in medical genomic analysis.The authors of the original article wer

270 CT-guided lung core needle biopsies used for genomic analysis, there should be a preference for using

271 vides a large-scale family level comparative genomic analysis to address genomic changes associated w

272 oyed transcriptome sequencing and population genomic analysis to describe patterns of genomic variati

273 We then performed an integrative genomic analysis to identify dysregulated molecules and

274 We have used quantitative genomic analysis to infer the key in vivo molecular para

275 Here, we used comparative genomic analysis to investigate the evolutionary history

276 We used genomic analysis to investigate the genetic basis of a d

277 me-coding genes, and facilitates comparative genomic analysis to study the evolutionary conservation

278 ere we apply a cell type-specific functional genomic analysis to the transcriptomes of auditory and v

279 complex dietary datasets, and the utility of genomic analysis to understand the relationships between

280 This Spatial Genomic Analysis toolkit provides a straightforward appr

281 everal well established and freely available genomic analysis tools to call SNPs and INDELs, and gene

282 we have adopted a suite of state-of-the-art genomic analysis tools to revisit the functional and met

283 Our comparative genomic analysis uncovers that the majority (26/29) of E

284 Genomic analysis was conducted for the non-typeable pneu

285 nnings of CHKi hypersensitivity, comparative genomic analysis was performed between hypersensitive ce

286 Functional genomic analysis was performed in S. cerevisiae and zebr

287 Detailed genomic analysis was performed on 180 of 194 patients wi

288 Genomic analysis was performed to quantify ARO spread be

289 Finally, a more thorough genomic analysis was performed, using CRISPR-Cas9 to del

290 Comparative genomics analysis was carried out among zoysiagrass, ric

291 Through genomic analysis, we also uncovered a feedback control o

292 Upon comparative genomic analysis, we found higher within-ST sequence div

293 Through comparative genomic analysis, we revealed that the extended CNLs (ex

294 In parallel to genomic analysis, we subjected the samples to gas chroma

295 therapeutic strategies, cell therapies, and genomic analysis were discussed.

296 , accessibility and auditability of pathogen genomic analysis while also supporting agency autonomy.

297 ommodate the needs of larger-scale microbial genomics analysis, while expanding GI predictions and im

298 Comparative genomic analysis with a focus on methylotrophy metabolis

299 nd 81.3% had stage IV disease at the time of genomic analysis, with prostate, renal, pancreatic, brea

300 R/Bioconductor packages to build a complete genomic analysis workflow entirely within the R environm