1 e often higher, which impacts the downstream
genomic analysis.
2 as surprisingly emerged from biochemical and
genomic analysis.
3 mapping with those from DNA sequencing-based
genomic analysis.
4 ly 1% D. mccartyi cells successfully enabled
genomic analysis.
5 sis for follow-up replication and functional
genomic analysis.
6 n and methylation profiling, for integrative
genomic analysis.
7 thelial-cells (BEC) of premature infants for
genomic analysis.
8 cular subtype was determined on the basis of
genomic analysis.
9 ease mutations discovered by high-throughput
genomic analysis.
10 related filamentous fungi using comparative
genomic analysis.
11 sing encapsulated stem cells of interest for
genomic analysis.
12 could not be detected either directly or by
genomic analysis.
13 n 2 affected siblings was deciphered through
genomic analysis.
14 ome coverage (0.21x to 3.93x) for population
genomic analysis.
15 All biopsy specimens had adequate yields for
genomic analysis.
16 24 (88%) of these had isolates available for
genomic analysis.
17 or properties can be highly complementary to
genomic analysis.
18 numerous sequences simultaneously, prior to
genomic analysis.
19 erum and identified by mass spectrometry and
genomic analysis.
20 ach related organism used in the comparative
genomics analysis.
21 vented a widespread application of genetical
genomics analysis.
22 ing demand for cloud-computing solutions for
genomics analysis.
23 ds and addresses the challenges of genetical
genomics analysis.
24 nformation has hitherto precluded functional
genomics analysis.
25 data and novel data derived from comparative
genomics analysis.
26 F-seq and used them to perform a comparative
genomics analysis.
27 ty induced by condition change in functional
genomics analysis.
28 nd PAH lung pericytes followed by functional
genomics analysis.
29 In order to facilitate
genomic analysis,
a fluorescence-activated cell sorting
30 While bulk tissue
genomic analysis across large populations of tumour cell
31 mutations that may have been missed through
genomic analysis alone.
32 SL precursor RNA (slRNA; 108-158 nt) through
genomic analysis and 3'-RACE technique, which was confir
33 Here, using
genomic analysis and a glioma mouse model, we demonstrat
34 Genomic analysis and biochemical assay strongly suggeste
35 4/08, and NDV-Belize-12/08) were assessed by
genomic analysis and by clinicopathological characteriza
36 Genomic analysis and deep RNA-Seq across infection time
37 alent DC have been identified by comparative
genomic analysis and functional studies in humans as XCR
38 mon file formats and data types used both in
genomic analysis and general data analysis.
39 structure and replicative cycle, along with
genomic analysis and genomic comparisons with previously
40 egrated Set Profile Analysis) for integrated
genomic analysis and its variation, SISPA (Sample Integr
41 In summary, integration of
genomic analysis and microRNA expression profiling could
42 Concurrent advances in tumor
genomic analysis and molecular inhibitor development hav
43 for distribution of specimens to pathology,
genomic analysis and PDX/cell line creation facilities;
44 on with Vanderbilt Technologies for Advanced
Genomics Analysis and Research Design (VANGARD), has dev
45 We employed a comparative
genomic analysis approach using the 28 isolates comprisi
46 e performed a comparative transcriptomic and
genomic analysis at the level of one single plant cell t
47 EY MESSAGE: A comparative transcriptomic and
genomic analysis between Arabidopsis thaliana and Glycin
48 Here we apply comparative functional
genomic analysis between C. elegans and Caenorhabditis b
49 Comparative
genomic analysis between tambaqui and zebrafish revealed
50 ext-generation sequencing is revolutionizing
genomic analysis,
but this analysis can be compromised b
51 Genomic analysis by massively parallel sequencing of 504
52 loited to enhance high-throughput functional
genomic analysis by tighter integration of data analyses
53 We found that large-scale
genomic analysis can identify nearly all known cancer ge
54 l malignancy, we conducted a high-resolution
genomic analysis combining DNA (23 samples) and mRNA (12
55 Integrative
genomic analysis,
combining global occupancy of Lsd1, ge
56 Genomic analysis continues to characterize genes and gen
57 Genomic analysis coupled with proteomic validation revea
58 By
genomic analysis,
cyclin E was amplified in 19.0% of the
59 XD2A-HTRA1 fusion in 12/125 (10%) cases, and
genomic analysis demonstrated the mechanism as resulting
60 Thus, integrative
genomic analysis demonstrates that ERG causes myeloid pr
61 sequencing data has improved the results of
genomic analysis due to the resolution of mapping algori
62 ulti-scale insight across multiple layers of
genomic analysis (
e.g., differential expression analysis
63 Here we demonstrate using
genomic analysis,
electron cryomicroscopy, and image rec
64 ion dynamic modelling and CML patient biopsy
genomic analysis enables patient stratification at unpre
65 vastly expanded as the result of comparative
genomic analysis,
followed by experimental validation.
66 Here, we report the largest
genomic analysis for puberty timing in 55,871 men, based
67 irected acyclic graphs (DAGs) in a genetical
genomics analysis framework.
68 Our
genomic analysis has also revealed that DSBR at the lacZ
69 Genomic analysis has connected altered astrocytic gene e
70 Comparative
genomic analysis has found an unprecedented degree of ge
71 Genomic analysis has greatly influenced the diagnosis an
72 Single-cell
genomic analysis has grown rapidly in recent years and f
73 Comparative
genomic analysis has led to the discovery of a new class
74 In recent years,
genomic analysis has provided extensive evidence of wide
75 However, preliminary
genomic analysis has suggested that genome-guided approa
76 while considering genetic markers, genetical
genomics analysis has shown its power in enhancing the u
77 In summary, our functional
genomics analysis highlighted novel genes and critical p
78 Comparative functional
genomic analysis identified a signature of Notch activat
79 udy, whole-genome sequencing and comparative
genomic analysis identified a unique Ent trilactone este
80 Our comparative
genomic analysis identified an expansion in the whale li
81 Comparative
genomic analysis identified genes that were unique to ea
82 Here, integrative
genomic analysis identified MYST3 as a potential oncogen
83 Genomic analysis identified selection for changes in mot
84 Integrative
genomic analysis identified SMPD3 and NEFH as tumor supp
85 Our comparative
genomic analysis identifies chromosome-level syntenic re
86 Here our integrative
genomic analysis identifies tousled-like kinase 2 (TLK2)
87 Here comparative
genomic analysis illustrates that UP-1s and UP-2s fall i
88 Using
genomic analysis,
immunoelectron microscopy, and two-pho
89 individual cells for whole-transcriptome or
genomic analysis in a massively parallel manner with min
90 eates tools and data resources to facilitate
genomic analysis in chordate species with an emphasis on
91 tion of conditional mutations for functional
genomic analysis in insects, and other organisms.
92 GenomeVIP has been used for
genomic analysis in large-data projects such as the TCGA
93 that evolutionary inference from integrated
genomic analysis in multisector biopsies can inform targ
94 of this study was to perform a comprehensive
genomic analysis in order to unravel the genomic archite
95 impact disease risk and support inclusion of
genomic analysis in the clinical management of AMGs.
96 We performed an integrative
genomic analysis,
incorporating whole exome sequencing (
97 Population
genomic analysis indicated a recent colonization ( appro
98 Comparative
genomic analysis indicated that angiosperms have two dis
99 Functional
genomic analysis indicated that SNPs in the TOMM40/APOE
100 Integrative
genomic analysis indicated that the transgenic enhancer
101 ding proteins CheV and CheW, and comparative
genomic analysis indicates a likely recent evolutionary
102 Comparative
genomic analysis indicates H24L5A's similarity to the Le
103 Genomic analysis is a powerful tool for understanding vi
104 important role in defining these conditions,
genomic analysis is providing a platform for better dise
105 A common practice in computational
genomic analysis is to use a set of 'background' sequenc
106 A common question in
genomic analysis is whether two sets of genomic interval
107 ISTA antibody in combination therapy and how
genomic analysis may assist in providing indications for
108 datasets combining the output from multiple
genomic analysis methods in an intuitive and interactive
109 The combination of improved
genomic analysis methods, decreasing genotyping costs, a
110 s demonstrate that pharmacotherapy guided by
genomic analysis,
molecular modeling, and functional pro
111 Based on comparative
genomic analysis of >6,000 sequenced bacteria from diver
112 Through
genomic analysis of 1,122 EGFR-mutant lung cancer cell-f
113 Comparative
genomic analysis of 129 and C57BL/6J mouse strains revea
114 ients with precursor B-cell ALL and detailed
genomic analysis of 154 patients with Ph-like ALL.
115 Genomic analysis of 18 emm1 isolates from Hong Kong and
116 Here we report
genomic analysis of 2,693 samples collected post mortem
117 rify the genomic basis of CTCL, we performed
genomic analysis of 220 CTCLs.
118 Using integrated
genomic analysis of 264 T-ALL cases, we identified 106 p
119 Here we perform a comparative
genomic analysis of 271 strains of conjunctivitis-causin
120 Comparative
genomic analysis of 28 S. Newport strains (including 2 r
121 We report
genomic analysis of 300 meningiomas, the most common pri
122 Here we present a multiplatform
genomic analysis of 37 patients with Sezary syndrome tha
123 Integrated
genomic analysis of 456 pancreatic ductal adenocarcinoma
124 A new study reports comparative
genomic analysis of 52 geographically diverse strains of
125 In a
genomic analysis of 78 FLC samples, we identified 3 clas
126 e results not only provide a high-resolution
genomic analysis of a bacterial pathogen during in vivo
127 We performed
genomic analysis of a congenital pigment synthesizing me
128 We performed an integrative
genomic analysis of a large series of patients with FLC
129 Genomic analysis of a large set of phages infecting the
130 that precision medicine approaches based on
genomic analysis of a single specimen are likely insuffi
131 This study provides a comprehensive
genomic analysis of A. actinomycetemcomitans and the clo
132 High-resolution structural and functional
genomic analysis of adult Burkitt lymphoma (BL) and high
133 f HGSCs, we report a multi-center integrated
genomic analysis of advanced stage tumors with and witho
134 , population genetic analysis and functional
genomic analysis of allelic activity.
135 nitiative, the most comprehensive up-to-date
genomic analysis of any Latin-American population.
136 estructive odontogenic tumors of the jaw, by
genomic analysis of archival material.
137 We present the first
genomic analysis of Atro using ChIP-seq against endogeno
138 Genomic analysis of barley paints a picture of diffuse o
139 We performed an integrative
genomic analysis of brain tissue-derived transcriptomes
140 also discuss connections revealed by recent
genomic analysis of cancers between chromothripsis, chro
141 Genomic analysis of chromothripsis and the search for it
142 We hypothesized that
genomic analysis of circulating free DNA (cfDNA) isolate
143 A
genomic analysis of colorectal cancer tissues identified
144 Through
genomic analysis of colorectal cancers and cell lines, w
145 Our method opens up the potential for
genomic analysis of contaminated fossil material.
146 on, here we perform integrated cross-species
genomic analysis of cuSCC development through the preneo
147 Genomic analysis of dominantly inherited, progressive se
148 Genomic analysis of drug response can provide unique ins
149 Here, we present a large-scale functional
genomic analysis of EBV.
150 Genomic analysis of FFPET from the 4 phenotype-positive/
151 examine a series of studies of molecular and
genomic analysis of glial tumours in children, and discu
152 Then, using an integrated epigenomic/
genomic analysis of Guthrie cards and follow-up sampling
153 identify H. haemolyticus Through comparative
genomic analysis of H. haemolyticus and NT H. influenzae
154 ch allow the first comprehensive comparative
genomic analysis of hepadnaviruses from four classes of
155 gh sensitivity of the algorithm also enables
genomic analysis of heterogeneous pathogen genomes from
156 Genomic analysis of high-altitude populations residing i
157 en followed by comparison against functional
genomic analysis of human and rodent beta cells exposed
158 p-based IRE1alpha interactome and functional
genomic analysis of human and rodent beta cells exposed
159 Large-scale
genomic analysis of human cancers indicates that the los
160 A recent integrative
genomic analysis of human prostate cancers (PCas) has re
161 We performed an integrative
genomic analysis of ICC samples from a large series of p
162 Genomic analysis of isolated CTCs revealed considerable
163 Genomic analysis of isolates identified several candidat
164 Genomic analysis of longevity offers the potential to il
165 Bioinformatic and
genomic analysis of LOS biosynthetic genes indicated sig
166 Comparative
genomic analysis of mouse L-R mammary gene expression pr
167 Genomic analysis of mouse neoplasms induced by the Dnajb
168 and inform treatment decisions.Significance:
Genomic analysis of multiple individual cells harvested
169 We performed
genomic analysis of new and published data from 249 PLGG
170 Here we report comparative
genomic analysis of nine isogenic iPSC lines generated u
171 he aim of the present study was to perform a
genomic analysis of non-specific lipid-transfer proteins
172 However, the functional
genomic analysis of one chromosome, its smallest, had al
173 Genomic analysis of our cohort further identified mutati
174 Comparative
genomic analysis of p53-targets in mouse and human ESCs
175 In summary, by coupling the systematic
genomic analysis of purified cancer cells in distinct ma
176 However,
genomic analysis of recent EPEC isolates has revealed th
177 Here, through a comparative
genomic analysis of replication origins and chromosomal
178 We performed
genomic analysis of RMS cells derived from a 27-year-old
179 With the use of serial
genomic analysis of samples collected at different point
180 To date, comprehensive
genomic analysis of SBA is lacking.
181 We show here a detailed
genomic analysis of single colorectal cancer-derived CTC
182 first time that it also enables comparative
genomic analysis of strain variation in a pathogen captu
183 Genomic analysis of Streptococcus thermophilus revealed
184 A recent
genomic analysis of Synechococcus cyanophages sampled fo
185 Comparative
genomic analysis of the accessory genome of the extant S
186 Although high homology complicates
genomic analysis of the ATAD3 defects, they can be ident
187 Starting from
genomic analysis of the cilia-associated transcription f
188 Advanced
genomic analysis of the entire spectrum of pediatric bra
189 Integrative
genomic analysis of the human AD brain transcriptome hol
190 Comparative
genomic analysis of the human LMOD1 and LMOD2 genes with
191 Here, comparative
genomic analysis of the MIPs was performed to investigat
192 A morphological, molecular and
genomic analysis of the post-embryonic phenotype of gct
193 We report here the sequencing and
genomic analysis of the SDR of Ectocarpus, a brown alga
194 It is anticipated that comparative
genomic analysis of this strain with other nitrate-depen
195 However, there has been little systematic
genomic analysis of this tumor type, and, thus, the cont
196 Genomic analysis of tumor biopsies revealed that vismode
197 They also have a strong influence on the
genomic analysis of tumour samples, and may alter the bi
198 Genomic analysis of tumours has led to the identificatio
199 Genomic analysis of WFBV revealed that it is most closel
200 we have conducted a comprehensive integrated
genomic analysis of young and aged cells.
201 re-based virtual screening with the chemical
genomics analysis of drug molecular signatures, and iden
202 Here we performed a systematic comparative
genomics analysis of human disease-causing missense vari
203 o our knowledge, the first global functional
genomics analysis of L. casei symbiosis.
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 By means of a comprehensive
genomic analysis on 6637 tissues of 21 tumor types, we h
208 Through comparative
genomic analysis,
one Red mutant PA1r was found to have
209 Genomic analysis predicts that C. trachomatis is capable
210 Combined with epidemiologic data, the
genomic analysis provides evidence of sexual transmissio
211 process from variant discovery to functional
genomics analysis,
resulting in an off-the-shelf toolkit
212 aditional sequencing methods, and downstream
genomic analysis results can be improved by correcting t
213 fic, long-term host association, comparative
genomic analysis revealed a deep divergence and little o
214 Genomic analysis revealed concentration-dependent action
215 Genomic analysis revealed deletions and amplifications i
216 Comparative
genomic analysis revealed differences among pseudomonads
217 Genomic analysis revealed genetic relatedness.
218 Genomic analysis revealed several interesting features o
219 Genomic analysis revealed significant alterations of org
220 Genomic analysis revealed that APT6V1A copy number is ga
221 Pan
genomic analysis revealed that BREX and BREX-like system
222 Here,
genomic analysis revealed that cultivated Z. latifolia h
223 Comparative
genomic analysis revealed that evolutionary conservation
224 Comparative
genomic analysis revealed that in the four readthrough c
225 m environment in both treatments, population
genomic analysis revealed that phages altered both the t
226 creatic ductal adenocarcinoma (PDAC) and our
genomic analysis revealed that SERPINB2 is frequently de
227 An integrative
genomic analysis revealed that the expression of genes a
228 Genomic analysis revealed that the fusion arose from tra
229 Genomic analysis revealed that the isolate lacked known
230 Genomic analysis revealed that these virulence-related g
231 Genomic analysis revealed that, in both parasitic and mu
232 Detailed
genomic analysis revealed the presence of gene homologs
233 Single-cell
genomic analysis reveals characteristic SCLC genomic cha
234 Comparative
genomic analysis reveals that all serovars encode a subs
235 Next, we used a novel in silico
genomic analysis,
searchable platform-independent expres
236 Genomic analysis showed that DSS3Phi8 is most closely re
237 In contrast, population
genomic analysis showed that genetic differentiation bet
238 Most importantly, a thorough
genomic analysis showed that the variants were generally
239 Genomic analysis showed that they contain a three-domain
240 Comparative
genomic analysis showed that two NOG1 copies are present
241 Population
genomic analysis shows a population bottleneck in this s
242 Genomic analysis shows that embryonal tumors have more s
243 Genomic analysis shows that Pst DC3000 carries a large r
244 oni, and Sphingopyxis alaskensis Comparative
genomic analysis shows that, in Enterobacteriaceae, the
245 ramework for the assessment of computational
genomics analysis skills, which includes standard operat
246 Genomic analysis strongly suggests EBOV transmission to
247 outinely used to obtain tissue for molecular
genomic analysis;
such analysis helps determine the diag
248 Genomic analysis suggested a route to regenerate the fum
249 Genomic analysis suggested higher intra- than inter-clad
250 has two inorganic phosphate (Pi) importers,
genomic analysis suggested that S. aureus possesses thre
251 phosphosites are not readily explainable by
genomic analysis,
suggesting that druggable translationa
252 Our
genomic analysis suggests replicative mechanisms as a pr
253 Genomic analysis suggests that DSS3Phi8 is a highly mosa
254 Our preliminary comparative
genomic analysis suggests that Hp0267 represents a secon
255 Genomic analysis suggests that the cancer first arose fr
256 ous oxidative product of folate degradation,
genomic analysis suggests that the first step of an unde
257 Our
genomic analysis suggests that the redox potential effec
258 A comparative
genomic analysis suggests that the reduction in energy m
259 This comparative
genomics analysis suggests a high degree of ORF conserva
260 ntroduce BEDOPS, a software suite for common
genomic analysis tasks which offers improved flexibility
261 re, we present a comprehensive proteomic and
genomic analysis that uncovered six major groups of PRC1
262 We present an integrated
genomic analysis that uncovers extensive intratumor hete
263 Through progress in clinical
genomic analysis,
the medical importance of this gene is
264 in order to address inequalities in medical
genomic analysis.
The authors of the original article wer
265 CT-guided lung core needle biopsies used for
genomic analysis,
there should be a preference for using
266 ing, in vitro experiments, metabolomics, and
genomic analysis to accelerate the identification of met
267 vides a large-scale family level comparative
genomic analysis to address genomic changes associated w
268 We used an integrative
genomic analysis to identify 2 classes of ICC.
269 Here, we used integrative
genomic analysis to identify candidate oncogenes in trip
270 We then performed an integrative
genomic analysis to identify dysregulated molecules and
271 We have used quantitative
genomic analysis to infer the key in vivo molecular para
272 We used
genomic analysis to investigate the genetic basis of a d
273 We use
genomic analysis to show that this motif is associated w
274 me-coding genes, and facilitates comparative
genomic analysis to study the evolutionary conservation
275 ere we apply a cell type-specific functional
genomic analysis to the transcriptomes of auditory and v
276 This Spatial
Genomic Analysis toolkit provides a straightforward appr
277 Existing
genomic analysis tools are often organized around litera
278 we have adopted a suite of state-of-the-art
genomic analysis tools to revisit the functional and met
279 Our comparative
genomic analysis uncovers that the majority (26/29) of E
280 Comparative
genomics analysis unravels lineage-specific bursts of ge
281 Comprehensive phenotyping and
genomic analysis utilizing nuclear families can provide
282 nnings of CHKi hypersensitivity, comparative
genomic analysis was performed between hypersensitive ce
283 Functional
genomic analysis was performed in S. cerevisiae and zebr
284 Detailed
genomic analysis was performed on 180 of 194 patients wi
285 Comparative
genomics analysis was carried out among zoysiagrass, ric
286 In this study, a comparative
genomics analysis was performed to identify EHEC-specifi
287 Using comparative
genomic analysis we identified the molecular genetic bas
288 Through
genomic analysis,
we also uncovered a feedback control o
289 Through
genomic analysis,
we further show that prokaryotes use d
290 Guided by this evolutionary
genomic analysis,
we generated a human-like E. coli dihy
291 Through comparative
genomic analysis,
we identified the orthologue gene of C
292 Here, through
genomic analysis,
we reveal that FoxA1 regulates two dis
293 In this
genomic analysis,
we sequenced the oldest extant Shigell
294 In parallel to
genomic analysis,
we subjected the samples to gas chroma
295 therapeutic strategies, cell therapies, and
genomic analysis were discussed.
296 ommodate the needs of larger-scale microbial
genomics analysis,
while expanding GI predictions and im
297 Comparative
genomic analysis with a focus on methylotrophy metabolis
298 Comparative
genomic analysis with Human Microbiome Project data reve
299 Comparative
genomic analysis with the type strain DSMZ10140 revealed
300 nd 81.3% had stage IV disease at the time of
genomic analysis,
with prostate, renal, pancreatic, brea