1 erentiation, which would confound downstream
genomic analyses).
2 esh-frozen tissue samples were collected for
genomic analyses.
3 A-gene interaction data into high-throughput
genomic analyses.
4 ters and subjected to integrated genetic and
genomic analyses.
5 le, yet powerful scripts that enable complex
genomic analyses.
6 acterium, we undertook comparative H. pylori
genomic analyses.
7 ncestry, is an essential step in comparative
genomic analyses.
8 isolating pure populations of stem cells for
genomic analyses.
9 nd as a prelude to comprehensive genetic and
genomic analyses.
10 by permitting highly informative comparative
genomic analyses.
11 valuation of publications that include human
genomic analyses.
12 ips, provides a model system for comparative
genomic analyses.
13 on functions, consistent with other previous
genomic analyses.
14 ollect enriched leukocytes for phenotype and
genomic analyses.
15 s a genetic risk index for MMI in behavioral
genomic analyses.
16 y hamper conventional genetic and functional
genomic analyses.
17 or disease states, similar to proteomic and
genomic analyses.
18 for k10(Mayer) and k10(C3H) by sequence and
genomic analyses.
19 lar alterations in 40 MECAs using integrated
genomic analyses.
20 d is proposed based on evidence from diverse
genomic analyses.
21 ryonic stem cells as shown by epigenetic and
genomics analyses.
22 hy away from publications that involve human
genomics analyses.
23 g practice of manual curation in comparative
genomics analyses.
24 Based on previous comparative
genomic analyses,
a set of nearly 600 polypeptides was i
25 ce, making the disease ideal for comparative
genomic analyses across species.
26 mes provides a rich resource for comparative
genomics analyses aimed at understanding the similaritie
27 more frequently than suggested by structural
genomic analyses alone.
28 Our
genomic analyses also provide useful resources for diet-
29 Integrated
genomic analyses also revealed mechanisms by which a sin
30 bly, targeted gene isolation and comparative
genomic analyses among grasses.
31 piratory symptoms and performed quantitative
genomic analyses among these and nine publicly available
32 Our C. albicans
genomic analyses and complementation studies in Saccharo
33 Mechanistically, cross-species
genomic analyses and complete ciliary rescue of knockout
34 o gain insights into GR suppression, we used
genomic analyses and genome-wide profiling of GR, p65, a
35 Chromatin-based functional
genomic analyses and genomewide association studies (GWA
36 We also used comparative
genomic analyses and reactive oxygen species burst assay
37 s of sufficient quality for most comparative
genomics analyses and for conservation genetics applicat
38 Comparative
genomics analyses and searches of the natural product ch
39 h high-throughput sequencing for comparative
genomics analyses and studies of genome evolution.
40 wo xylosyltransferases have been found using
genomic analyses,
and one of these, XylT1, has been show
41 th organisms, have resulted from comparative
genomic analyses,
and several have been experimentally c
42 Genomic analyses are defining the molecular architecture
43 The benefits of large-scale comparative
genomic analyses are driving the community to think abou
44 Although these
genomic analyses are informative, experimental verificat
45 Comparative
genomic analyses are now opening the way for refined fun
46 Population
genomic analyses are often hindered by difficulties in o
47 Targeted
genomic analyses are required to determine whether these
48 h, by reverse transcription-PCR (RT-PCR) and
genomic analyses,
are located in three similarly organiz
49 Comparative
genomic analyses based on the principle of evolutionary
50 These studies provide a roadmap to exploit
genomic analyses by directing investigations of pathogen
51 gical- and conservation-motivated population
genomic analyses by noncomputational biologists, the ana
52 and proteomic profile as well as comparative
genomic analyses can direct the progress of future resea
53 ases in the recent years the results of post-
genomic analyses can facilitate a better understanding o
54 eveal that a combination of histological and
genomic analyses can uncover substantial heterogeneity i
55 On the basis of
genomic analyses,
cobalamin biosynthesis in marine syste
56 Here we discuss the results of large-scale
genomic analyses conducted to date and review the most a
57 ds from all families and further genetic and
genomic analyses confirmed the WES-identified findings.
58 Integrated transcriptomic and
genomic analyses defined a distinct superenhancer in CIM
59 Phylogenetic and comparative
genomic analyses demonstrate that S. mansoni NRs share a
60 Extensive
genomic analyses demonstrated the concurrent circulation
61 Genomic analyses determined that LO28 contains a natural
62 Comparison of
genomic analyses (
DNA) with paired transcriptomic studie
63 a valuable resource for various genetic and
genomic analyses,
especially for GWAS and QTL mapping fo
64 Comparative
genomics analyses executed by powerful computer algorith
65 Genomic analyses failed to detect N-ras gene mutations i
66 Here we present sequence and
genomic analyses for 12 antibodies that pierce these def
67 Our comparative
genomic analyses found that convergent amino acid substi
68 Genomic analyses from blood leukocytes have concluded th
69 ees phylogenomics system pursues comparative
genomic analyses from the perspective of gene phylogenie
70 Comparative
genomic analyses further revealed that rs4305745 and/or
71 Interestingly,
genomic analyses have also hinted at the existence of a
72 Genomic analyses have associated host gene mutations wit
73 Genomic analyses have been applied extensively to analyz
74 S genome sequences are available, functional
genomic analyses have been limited.
75 So far, no comprehensive
genomic analyses have been performed to elucidate the mo
76 While
genomic analyses have been relatively extensive for cyan
77 Further
genomic analyses have found that all available fully seq
78 Genomic analyses have highlighted the importance of hori
79 Recent
genomic analyses have identified activating mutations, t
80 Cell line, tissue microarray, and
genomic analyses have identified additional targets incl
81 Genomic analyses have identified low CpG promoters that
82 Genomic analyses have identified the mutations that have
83 Genomic analyses have proliferated without being tied to
84 Recent
genomic analyses have revealed substantial tumor heterog
85 Our genetic and
genomic analyses have revealed that both VosA and VelB a
86 Comparative
genomic analyses have revealed that genes may arise from
87 Recent microarray-based comparative
genomic analyses have revealed that members of this spec
88 16S rRNA-based
genomic analyses have revolutionized our understanding o
89 Genomic analyses have shown that adjacent genes are ofte
90 Genomic analyses have the potential to impact selective
91 Recently,
genomics analyses have demonstrated that alternative spl
92 Bisulfite-mediated
genomic analyses identified different DNA methylation pa
93 In this study, comparative
genomic analyses identified orthologous genes of unknown
94 Inverse PCR combined with
genomic analyses identified P insertions within or close
95 Functional
genomics analyses identified cellular genes triggered du
96 Phylogenetic, cytogenetic, and
genomic analyses implied that the nonnative sequences we
97 rcome this problem and facilitate functional
genomic analyses in bifidobacteria, we created a large T
98 Recent
genomic analyses in Drosophila and mammals of inter-chro
99 In this study, we performed global
genomic analyses in murine embryonic stem (ES) cells and
100 Through germline
genomic analyses in patients with lens and eye abnormali
101 are disorders, and illustrate the utility of
genomic analyses in studying combined and variable pheno
102 se studies demonstrate the value of unbiased
genomic analyses in the characterization of human brain
103 genome size of polyploid wheat, had hindered
genomic analyses in this important crop species.
104 Comparative
genomic analyses in this study demonstrated genetic simi
105 titute an essential resource for genetic and
genomic analyses in X. tropicalis.
106 a prerequisite to virtually all comparative
genomic analyses,
including the identification of conser
107 Integrated
genomic analyses,
including whole-exome sequencing and c
108 Genomic analyses indicate date palm domestication occurr
109 Genomic analyses indicate multiple systems for reverse e
110 Comparative
genomic analyses indicate that differences have evolved
111 Integrative
genomic analyses indicate that KMT2D affects methylation
112 Comparative
genomics analyses indicate that this family is the most
113 Genomic analyses indicated immediate interference with t
114 Genomic analyses indicated that a full-length dectin-2 (
115 Genomic analyses indicated that lac repressors were co-s
116 Integrated miRNA- and mRNA-based
genomic analyses indicated that miR-183 is an important
117 Genomic analyses indicated that Pitx2 activated genes en
118 Genomic analyses indicated that the +9.5 element regulat
119 Genomic analyses indicated that these traits are mainly
120 Comparative
genomic analyses investigated the conservation of KCNMA1
121 ability of genomic tools and advancements in
genomic analyses,
it is becoming increasingly clear that
122 Genomic analyses of 10 strains demonstrated that H. haem
123 Here we report comprehensive
genomic analyses of 49 individuals with chondrosarcoma (
124 9 patient-derived tumour grafts and targeted
genomic analyses of 55 patient tumours, all of which wer
125 whole-exome analyses of 24 tumours, targeted
genomic analyses of 77 tumours, and use non-invasive app
126 he basis of a combination of next-generation
genomic analyses of 775 meningiomas, we report that recu
127 is study, we used comparative and population
genomic analyses of 92 genomes from eight phylogenetical
128 Genome sequencing and comparative
genomic analyses of 94 previously uncharacterized ETEC i
129 Genomic analyses of a few representatives suggested that
130 and (3) potentially enable new proteomic and
genomic analyses of activity-regulated molecules in an i
131 Genomic analyses of AS are also at a nascent stage, but
132 Genomic analyses of available S. pyogenes genomes reveal
133 IMAG will facilitate more robust comparative
genomic analyses of bacterial and archaeal diversity.
134 Comparative
genomic analyses of Candida glabrata and Saccharomyces c
135 By couching population
genomic analyses of chemosensory protein families within
136 analyses of natural populations, comparative
genomic analyses of closely related species, identificat
137 Comprehensive
genomic analyses of common nervous system cancers provid
138 We carried out comparative
genomic analyses of copper, molybdenum, nickel, cobalt (
139 Genomic analyses of cutaneous melanoma (CM) have yielded
140 To support various functional
genomic analyses of DC3000, and specifically, to identif
141 Until recently, genetic and
genomic analyses of division of labour were limited to j
142 Genomic analyses of Drosophila species suggest that the
143 Recent
genomic analyses of Escherichia coli O157:H7 strain EDL9
144 Here we describe the
genomic analyses of four DNA samples from an African-Ame
145 In addition, there are opportunities for
genomic analyses of genetic polymorphisms and the gut mi
146 Genomic analyses of GMPs, including gene expression and
147 computational approach involving comparative
genomic analyses of human and mouse orthologous genes un
148 Large-scale
genomic analyses of human cancers have cataloged somatic
149 ic origins of aneuploidy through integrative
genomic analyses of human tumors.
150 I review here evolutionary and comparative
genomic analyses of insect antimicrobial immune genes, w
151 er to antiangiogenesis therapy, we conducted
genomic analyses of intraperitoneal ovarian tumors in wh
152 Phylogenetic and population
genomic analyses of isolates from Brazil reveal that the
153 idate gain-of-function genes defined through
genomic analyses of large patient cohorts offers an attr
154 Genomic analyses of late-stage human cancers have uncove
155 des a platform which will be of use for post-
genomic analyses of Leishmania cell biology in relation
156 However,
genomic analyses of living species that have survived a
157 w research tools for physical and functional
genomic analyses of M. domestica that are expanding its
158 Genomic analyses of many solid cancers have demonstrated
159 f the "reverse-methanogenesis" hypothesis by
genomic analyses of methane-oxidizing Archaea from deep-
160 Genomic analyses of microbial populations in their natur
161 reased activity of SIRT1 was validated using
genomic analyses of mouse models of lung cancer and bioc
162 Genomic analyses of MPNSTs arising in neuregulin-1 and e
163 We have conducted
genomic analyses of multiple strains from the UK outbrea
164 ed from bacteria that was discovered through
genomic analyses of naturally occuring marine bacteriopl
165 lts are presented from separate and combined
genomic analyses of new and previously published data, i
166 Genomic analyses of Nhp6A mutants specifically defective
167 In-depth
genomic analyses of one tumor followed by immunohistoche
168 Recent
genomic analyses of pathologically defined tumor types i
169 Recent
genomic analyses of pediatric glioblastoma, a poorly und
170 We report here
genomic analyses of planktonic microbial communities in
171 Genomic analyses of pre-neoplastic tumors and diagnostic
172 inical trials of bortezomib and consented to
genomic analyses of pretreatment tumor samples.
173 Comparative
genomic analyses of primary tumors and metastases within
174 Genomic analyses of probands with heterotaxy, atrial sep
175 Comparative
genomic analyses of prokaryotic species as they are pres
176 Moreover,
genomic analyses of promoter regions suggested that the
177 Genomic analyses of prostate cancer reveal distinct patt
178 Genomic analyses of recurrent tumors revealed multiple l
179 We performed comparative functional
genomic analyses of representatives of 25 species of Lac
180 he nature and composition of the protomap by
genomic analyses of spatial and temporal neocortical pro
181 Comparative
genomic analyses of stratified microbial communities hav
182 In subgenomic and
genomic analyses of subcellular mRNA partitioning, we re
183 Genomic analyses of taxonomically related Bordetella and
184 Comparative
genomic analyses of the closely related nonhypervirulent
185 Here, we describe our
genomic analyses of the initial and recurrent tumor spec
186 Genomic analyses of the localization and expression dyna
187 Genomic analyses of the myeloid malignancies and clonal
188 Complete
genomic analyses of the opossum TCR loci continue to sup
189 these new data we have conducted a series of
genomic analyses of the OR and V1R genes from mouse and
190 Here we report
genomic analyses of the photosynthetic gene content and
191 Population
genomic analyses of these data support the hypothesis of
192 Genomic analyses of these novel bacteriophages yielded m
193 ntatives of the bacterial phylum Firmicutes,
genomic analyses of these organisms have yet to be repor
194 in-coding genes, and completed comprehensive
genomic analyses of this obligate blood-feeding insect.
195 Genomic analyses of this productive group of bacteria sh
196 Population
genomic analyses of whole-genome sequences from 32 indiv
197 Population
genomics analyses of 20 O. glaberrima and 94 Oryza barth
198 olation of genes/QTL, conducting comparative
genomics analyses of plant chromosomes, and large-scale
199 Here we show, using integrated imaging-
genomics analyses of primary human fibroblasts, that upr
200 Population genetics and comparative
genomics analyses of the pathogenic Yersinia species hav
201 We performed extensive
genomic analyses on a panel of cancer cell lines and nar
202 -like" conditions on microglia, we performed
genomic analyses on wild-type (WT) and TLR4(-/-) culture
203 unocompromised host, we performed functional
genomics analyses on control and Stat1(-/-) mouse cornea
204 Consequently,
genomic analyses promise to generate important new insig
205 Genomic analyses promise to improve tumor characterizati
206 Comparative
genomic analyses provide important clues about the evolu
207 gene prediction with genetic and comparative
genomic analyses provide insight regarding the functiona
208 Virus population
genomic analyses provided evidence that extensive recomb
209 However, recent work using high throughput
genomic analyses questions the accuracy of this assumpti
210 Using a combination of
genomic analyses,
receptor imaging, ligand identificatio
211 We performed comparative
genomic analyses representing lineages of nearly all ext
212 Genomic analyses reveal a broad mutational spectrum uniq
213 Genomic analyses reveal how this revolutionary signaling
214 Further
genomic analyses reveal mouse mammary tumors growing ind
215 Population
genomic analyses reveal reduced polymorphism in centrome
216 Our integrated
genomic analyses reveal that H2A.Z.2 controls the transc
217 Genomic analyses reveal that macroH2A1 and macroH2A2, to
218 Genomic analyses reveal that multiple mechanisms exist f
219 Genomic analyses reveal that up 1.7% of all identified h
220 Overall, comparative and
genomic analyses reveal the emergence of a new group or
221 cDNA and
genomic analyses reveal the existence of multiple forms
222 Genomic analyses revealed (11) prevalence of strains fro
223 Integrated
genomic analyses revealed a miRNA-regulatory network tha
224 Genomic analyses revealed a potential locus dedicated to
225 Genomic analyses revealed a putative chemoreceptor-encod
226 Recent
genomic analyses revealed a surprisingly large number of
227 Further phylogenetic and population
genomic analyses revealed extensive loss of genetic dive
228 Genomic analyses revealed genes and pathways that associ
229 Comparative
genomic analyses revealed high similarities between the
230 Population
genomic analyses revealed microdiversity within bacteria
231 Here, comparative
genomic analyses revealed that a local duplication of an
232 Genomic analyses revealed that the 1918 virus blocked th
233 Subsequent phylogenetic and comparative
genomic analyses revealed that the Central North Pacific
234 Genomic analyses revealed that three Yellowstone Lake ph
235 us is still obscure, our previous functional
genomics analyses revealed a correlation between the let
236 Computational
genomics analyses revealed increased activity of NF-kapp
237 Our molecular population
genomic analyses show higher deletion than insertion mut
238 Various
genomic analyses show that all examined humans are homoz
239 Genomic analyses show that Perkinsela sp. has lost the a
240 Comparative
genomic analyses show that the genome of M. purpureus is
241 In addition, comparative
genomic analyses show that the typical mouse, rat, and m
242 Genomic analyses showed that certain species are specifi
243 Further functional
genomic analyses showed that eSTRs are enriched in conse
244 Functional
genomic analyses showed that soluble (s) IL-1RII, at pic
245 Population
genomic analyses showed that, whereas the majority of hu
246 The recent combined use of mutants,
genomic analyses,
sophisticated spectroscopies, and live
247 discussed, since it underlies all secondary
genomic analyses such as RNA sequencing (RNA-Seq), chrom
248 Solid tumors present several challenges for
genomic analyses,
such as tumor heterogeneity and tumor
249 Nonetheless, comparative
genomic analyses suggest that a significant rate differe
250 Recent
genomic analyses suggest that promoter-promoter interact
251 Genomic analyses suggest that similar markers are also l
252 s of pathogenic fungi and bacteria; however,
genomic analyses suggest that the majority of microbial
253 Phylogenetic and comparative
genomic analyses suggest that the structures have arisen
254 Comparative
genomic analyses suggest that this pathway, encoded in a
255 Integrative
genomic analyses suggested that the aberrant expression
256 Epidemiological and
genomic analyses suggested that the anaconda juveniles a
257 Genetic and
genomic analyses support the conclusion that these effec
258 Prompted by recent
genomic analyses that identified cyclin E1 (CCNE1) gene
259 de association studies and other large-scale
genomic analyses that require robust, high-accuracy geno
260 As we expand the breadth and depth of
genomic analyses,
the biological and clinical complexity
261 Coupled with
genomic analyses,
these results point to sporulation as
262 f WormBase with the inclusion of large-scale
genomic analyses,
through active data and literature cur
263 current genome assemblies and, consequently,
genomic analyses to date have excluded rDNA.
264 control subjects, and performed integrative
genomic analyses to define methylation-gene expression r
265 We combined conventional and
genomic analyses to define the duration and scale of a l
266 s were subjected to a battery of comparative
genomic analyses to determine their level of relatedness
267 We used
genomic analyses to determine whether superficial behavi
268 lementing high-resolution, multiple-platform
genomic analyses to discover small and subtle, but funct
269 gy and evolutionary history into comparative
genomic analyses to elucidate how P. syringae subverts t
270 Here we use comprehensive genetic and
genomic analyses to follow muscle development in a mouse
271 functional genetic screens and comprehensive
genomic analyses to identify CDK6 as a GBM oncogene that
272 r of combining gene expression profiling and
genomic analyses to identify susceptibility genes for ge
273 matic analyses can be of high importance for
genomic analyses to provide full predictions of translat
274 g and integrated phylogenomic and population
genomic analyses to study hybridization and reconstruct
275 Here, we discuss the results of these
genomic analyses,
together with the current literature,
276 rs of magnitude faster turnaround for common
genomic analyses,
transforming long-running batch jobs s
277 Comparative
genomic analyses uncovered evolutionarily conserved cons
278 Genomic analyses uncovered four distinct genes that allo
279 Genomic analyses using RNA-seq and ER ChIP-seq demonstra
280 Comparative
genomic analyses utilizing a gene-independent whole-geno
281 Using comparative
genomic analyses,
we examined complete mitochondrial gen
282 imprinted gene network (IGN) into functional
genomic analyses,
we found that H19 mediates suppression
283 Through comparative
genomic analyses,
we identified a gene, denoted cpcM, th
284 Using comparative
genomic analyses,
we identified genes unique to L. lacti
285 combination of phylogenetic and comparative
genomic analyses,
we then investigated the evolution of
286 Using complementary
genomics analyses,
we identified the interferon pathway
287 Population
genomic analyses were done with a hierarchical gene-by-g
288 Functional
genomic analyses were performed to assess the relationsh
289 Genomic analyses were performed using haplotype sharing
290 Comparative
genomic analyses were performed with these strains and t
291 In this report, comparative
genomic analyses were used to identify and characterize
292 embers, phylogenetic and several comparative
genomics analyses were performed.
293 Comprehensive bioinformatics and functional
genomics analyses were used to identify key regulators,
294 Genomic analyses (
whole genome, exome, and transcriptome
295 trophysiological, molecular, and integrative
genomic analyses with focus on schizophrenia-relevant pa
296 uces a high cellular yield for cytologic and
genomic analyses with minimal risk of extraocular dissem
297 Comparative
genomic analyses with the complete DNA sequence of M. tu
298 Comparative
genomics analyses with uncultivated environmental TM7 as
299 ing technologies have placed a wide range of
genomic analyses within the capabilities of many laborat
300 any comparative, evolutionary and functional
genomic analyses,
yet the true evolutionary history of g