1 erentiation, which would confound downstream
genomic analyses).
2 d is proposed based on evidence from diverse
genomic analyses.
3 on planning and can be applied to downstream
genomic analyses.
4 lar alterations in 40 MECAs using integrated
genomic analyses.
5 esh-frozen tissue samples were collected for
genomic analyses.
6 A-gene interaction data into high-throughput
genomic analyses.
7 very are essential to leverage insights from
genomic analyses.
8 ters and subjected to integrated genetic and
genomic analyses.
9 le, yet powerful scripts that enable complex
genomic analyses.
10 acterium, we undertook comparative H. pylori
genomic analyses.
11 and immune cell measurements and single-cell
genomic analyses.
12 bally distributed clades based on population
genomic analyses.
13 1 ALL evidenced by both germline and somatic
genomic analyses.
14 f new genes has been well documented through
genomic analyses.
15 ously considered in contemporary comparative
genomic analyses.
16 ally enhance the scalability and accuracy of
genomic analyses.
17 g practice of manual curation in comparative
genomics analyses.
18 ryonic stem cells as shown by epigenetic and
genomics analyses.
19 Based on previous comparative
genomic analyses,
a set of nearly 600 polypeptides was i
20 ce, making the disease ideal for comparative
genomic analyses across species.
21 more frequently than suggested by structural
genomic analyses alone.
22 Our
genomic analyses also provide useful resources for diet-
23 Integrated
genomic analyses also revealed mechanisms by which a sin
24 bly, targeted gene isolation and comparative
genomic analyses among grasses.
25 assemblies form the basis of most downstream
genomic analyses and are of critical importance.
26 HDL brings more power to
genomic analyses and better reveals the underlying conne
27 Our C. albicans
genomic analyses and complementation studies in Saccharo
28 Mechanistically, cross-species
genomic analyses and complete ciliary rescue of knockout
29 Bulk
genomic analyses and expression profiling of clinical sp
30 o gain insights into GR suppression, we used
genomic analyses and genome-wide profiling of GR, p65, a
31 Chromatin-based functional
genomic analyses and genomewide association studies (GWA
32 otypes across species can inform comparative
genomic analyses and improve gene annotations.
33 t biological specimens from participants for
genomic analyses and indefinite storage.
34 We also used comparative
genomic analyses and reactive oxygen species burst assay
35 s of sufficient quality for most comparative
genomics analyses and for conservation genetics applicat
36 h high-throughput sequencing for comparative
genomics analyses and studies of genome evolution.
37 Here, we combine experimental microbiology,
genomic analyses,
and Earth system modeling to demonstra
38 Through the use of simulations,
genomic analyses,
and high throughput splicing assays, w
39 Genomic analyses are defining the molecular architecture
40 Comparative
genomic analyses are now opening the way for refined fun
41 Population
genomic analyses are often hindered by difficulties in o
42 Targeted
genomic analyses are required to determine whether these
43 Genomic analyses are sensitive to contamination in publi
44 h, by reverse transcription-PCR (RT-PCR) and
genomic analyses,
are located in three similarly organiz
45 Pan-cancer
genomic analyses based on the magnitude of pathway activ
46 Comparative
genomic analyses based on the principle of evolutionary
47 These studies provide a roadmap to exploit
genomic analyses by directing investigations of pathogen
48 gical- and conservation-motivated population
genomic analyses by noncomputational biologists, the ana
49 On the basis of
genomic analyses,
cobalamin biosynthesis in marine syste
50 Here we discuss the results of large-scale
genomic analyses conducted to date and review the most a
51 ds from all families and further genetic and
genomic analyses confirmed the WES-identified findings.
52 Integrated transcriptomic and
genomic analyses defined a distinct superenhancer in CIM
53 Deep comparative
genomic analyses demonstrated that this miR2275/24-nt ph
54 Genomic analyses determined that LO28 contains a natural
55 Comparison of
genomic analyses (
DNA) with paired transcriptomic studie
56 Advances in
genomic analyses enable the identification of new protei
57 a valuable resource for various genetic and
genomic analyses,
especially for GWAS and QTL mapping fo
58 Comparative
genomics analyses executed by powerful computer algorith
59 ghlights the value of comparative population
genomic analyses for gauging the evolutionary processes
60 Comparative
genomic analyses found signatures of positive selection
61 Our comparative
genomic analyses found that convergent amino acid substi
62 Genomic analyses from blood leukocytes have concluded th
63 me, detailed archaeological information, and
genomic analyses from infected individuals and hundreds
64 Genomic analyses further revealed that the Whi2p-Psr1p/P
65 Genomic analyses have associated host gene mutations wit
66 S genome sequences are available, functional
genomic analyses have been limited.
67 So far, no comprehensive
genomic analyses have been performed to elucidate the mo
68 While
genomic analyses have been relatively extensive for cyan
69 Recent
genomic analyses have identified activating mutations, t
70 Cell line, tissue microarray, and
genomic analyses have identified additional targets incl
71 Indeed,
genomic analyses have identified four major groups of ta
72 Genomic analyses have identified low CpG promoters that
73 Genomic analyses have identified that the cohesin subuni
74 Genomic analyses have identified the mutations that have
75 Genomic analyses have proliferated without being tied to
76 Genomic analyses have provided transformative knowledge
77 Recent
genomic analyses have revealed substantial tumor heterog
78 Our genetic and
genomic analyses have revealed that both VosA and VelB a
79 Comparative
genomic analyses have revealed that genes may arise from
80 16S rRNA-based
genomic analyses have revolutionized our understanding o
81 Comparative
genomic analyses have shown that core components of the
82 Genomic analyses have shown that demographic processes s
83 Genomic analyses have the potential to impact selective
84 In the previous decade, comprehensive
genomic analyses have yielded important insights about t
85 Genomic analyses identified a distinct molecular subgrou
86 Genomic analyses identified a diverse set strains in inf
87 Bisulfite-mediated
genomic analyses identified different DNA methylation pa
88 In this study, comparative
genomic analyses identified orthologous genes of unknown
89 Comparative
genomics analyses identify extensive structural variatio
90 Phylogenetic, cytogenetic, and
genomic analyses implied that the nonnative sequences we
91 Efforts from the past decade in
genomic analyses improved our understanding of genetic s
92 rcome this problem and facilitate functional
genomic analyses in bifidobacteria, we created a large T
93 Recent
genomic analyses in Drosophila, however, show that gene
94 In this study, we performed global
genomic analyses in murine embryonic stem (ES) cells and
95 Through germline
genomic analyses in patients with lens and eye abnormali
96 are disorders, and illustrate the utility of
genomic analyses in studying combined and variable pheno
97 genome size of polyploid wheat, had hindered
genomic analyses in this important crop species.
98 Comparative
genomic analyses in this study demonstrated genetic simi
99 titute an essential resource for genetic and
genomic analyses in X. tropicalis.
100 es, we provide examples from high-throughput
genomic analyses,
including chromatin immunoprecipitatio
101 A range of
genomic analyses,
including mNET-seq, 3' mRNA-seq, chrom
102 Integrated
genomic analyses,
including whole-exome sequencing and c
103 Genomic analyses indicate date palm domestication occurr
104 Genomic analyses indicate multiple systems for reverse e
105 Integrative
genomic analyses indicate that KMT2D affects methylation
106 Comparative
genomic analyses indicate that RiTBi may be a relatively
107 Because integrated clinical and
genomic analyses indicate that similar pathways are acti
108 Genomic analyses indicate that these individuals are gen
109 Comparative
genomics analyses indicate that this family is the most
110 Genomic analyses indicated immediate interference with t
111 Genomic analyses indicated that lac repressors were co-s
112 Integrated miRNA- and mRNA-based
genomic analyses indicated that miR-183 is an important
113 Genomic analyses indicated that Pitx2 activated genes en
114 Genomic analyses indicated that the +9.5 element regulat
115 Genomic analyses indicated that these traits are mainly
116 ability of genomic tools and advancements in
genomic analyses,
it is becoming increasingly clear that
117 Genomic analyses of 10 strains demonstrated that H. haem
118 Genomic analyses of 258 RMS patient tumors uncovered pre
119 Here we report comprehensive
genomic analyses of 49 individuals with chondrosarcoma (
120 9 patient-derived tumour grafts and targeted
genomic analyses of 55 patient tumours, all of which wer
121 whole-exome analyses of 24 tumours, targeted
genomic analyses of 77 tumours, and use non-invasive app
122 he basis of a combination of next-generation
genomic analyses of 775 meningiomas, we report that recu
123 is study, we used comparative and population
genomic analyses of 92 genomes from eight phylogenetical
124 Genome sequencing and comparative
genomic analyses of 94 previously uncharacterized ETEC i
125 Genomic analyses of a few representatives suggested that
126 Here
genomic analyses of anatomically modern humans, extinct
127 Genomic analyses of available S. pyogenes genomes reveal
128 IMAG will facilitate more robust comparative
genomic analyses of bacterial and archaeal diversity.
129 By couching population
genomic analyses of chemosensory protein families within
130 analyses of natural populations, comparative
genomic analyses of closely related species, identificat
131 Comprehensive
genomic analyses of common nervous system cancers provid
132 In this review, we describe how
genomic analyses of coronary artery disease have been le
133 Genomic analyses of cutaneous melanoma (CM) have yielded
134 Genomic analyses of diverse strains of Bacteroidetes fro
135 Genomic analyses of Drosophila species suggest that the
136 tous coccolithophore genus Gephyrocapsa with
genomic analyses of extant species to assess the genetic
137 olution mycobiota sequencing and comparative
genomic analyses of fecal and blood specimens from recip
138 Population
genomic analyses of Ficus species revealed genomic signa
139 Genomic analyses of flow-sorted, dominant sheath-water b
140 Here we describe the
genomic analyses of four DNA samples from an African-Ame
141 ur results highlight that precise functional
genomic analyses of GABA(A) receptor mutations using con
142 In addition, there are opportunities for
genomic analyses of genetic polymorphisms and the gut mi
143 Genomic analyses of GMPs, including gene expression and
144 phalosporins and azithromycin using detailed
genomic analyses of gonococcal isolates collected in the
145 To date,
genomic analyses of hepatocellular carcinoma (HCC) have
146 Here, we conducted
genomic analyses of heterozygous and homozygous Chd8 mou
147 Large-scale
genomic analyses of human cancers have cataloged somatic
148 ased expression-findings that, combined with
genomic analyses of human height, explain ~12% of the di
149 ic origins of aneuploidy through integrative
genomic analyses of human tumors.
150 er to antiangiogenesis therapy, we conducted
genomic analyses of intraperitoneal ovarian tumors in wh
151 Phylogenetic and population
genomic analyses of isolates from Brazil reveal that the
152 idate gain-of-function genes defined through
genomic analyses of large patient cohorts offers an attr
153 des a platform which will be of use for post-
genomic analyses of Leishmania cell biology in relation
154 However,
genomic analyses of living species that have survived a
155 Genomic analyses of many solid cancers have demonstrated
156 Genomic analyses of microbial populations in their natur
157 reased activity of SIRT1 was validated using
genomic analyses of mouse models of lung cancer and bioc
158 Genomic analyses of MPNSTs arising in neuregulin-1 and e
159 We have conducted
genomic analyses of multiple strains from the UK outbrea
160 Genomic analyses of Nhp6A mutants specifically defective
161 will improve greatly our ability to perform
genomic analyses of non-O1 V. cholerae in the future.
162 In-depth
genomic analyses of one tumor followed by immunohistoche
163 Recent
genomic analyses of pathologically defined tumor types i
164 Genomic analyses of patients with congenital heart disea
165 Recent
genomic analyses of pediatric glioblastoma, a poorly und
166 ectors, enabling evolutionary and population
genomic analyses of Phytophthora species.
167 Comparative
genomic analyses of primary tumors and metastases within
168 Genomic analyses of probands with heterotaxy, atrial sep
169 Moreover,
genomic analyses of promoter regions suggested that the
170 Genomic analyses of prostate cancer reveal distinct patt
171 Genomic analyses of recurrent tumors revealed multiple l
172 We performed comparative functional
genomic analyses of representatives of 25 species of Lac
173 Genomic analyses of several rattlesnake (Crotalus) speci
174 In subgenomic and
genomic analyses of subcellular mRNA partitioning, we re
175 Genomic analyses of taxonomically related Bordetella and
176 Comparative
genomic analyses of the closely related nonhypervirulent
177 Here, we describe our
genomic analyses of the initial and recurrent tumor spec
178 Genomic analyses of the myeloid malignancies and clonal
179 Population
genomic analyses of these data support the hypothesis of
180 Genomic analyses of these isolates along with those isol
181 Genomic analyses of these novel bacteriophages yielded m
182 in-coding genes, and completed comprehensive
genomic analyses of this obligate blood-feeding insect.
183 Genomic analyses of this productive group of bacteria sh
184 Population
genomic analyses of whole-genome sequences from 32 indiv
185 Population
genomics analyses of 20 O. glaberrima and 94 Oryza barth
186 Here we show, using integrated imaging-
genomics analyses of primary human fibroblasts, that upr
187 ,001 stool, 559 environment) and focused our
genomic analyses on 1,477 isolates (95%) in the hospital
188 rehensive study incorporating epigenetic and
genomic analyses on a large cohort of brainstem gliomas,
189 We performed extensive
genomic analyses on a panel of cancer cell lines and nar
190 putational tool that facilitates large-scale
genomic analyses on public and academic clouds.
191 -like" conditions on microglia, we performed
genomic analyses on wild-type (WT) and TLR4(-/-) culture
192 Our work, including
genomic analyses,
phenotypic assays, and identification
193 The nations believed the proposed
genomics analyses presented a risk of harm to their peop
194 Consequently,
genomic analyses promise to generate important new insig
195 Genomic analyses promise to improve tumor characterizati
196 Moreover, our comparative
genomics analyses provide novel insights into Carnivora
197 e genomes allows functional and evolutionary
genomic analyses providing genome-wide evidence for gene
198 Using a combination of
genomic analyses,
receptor imaging, ligand identificatio
199 We performed comparative
genomic analyses representing lineages of nearly all ext
200 Genomic analyses reveal a broad mutational spectrum uniq
201 Genomic analyses reveal how this revolutionary signaling
202 Further
genomic analyses reveal mouse mammary tumors growing ind
203 Population
genomic analyses reveal reduced polymorphism in centrome
204 Comparative
genomic analyses reveal specific gene expansions in the
205 Comparative
genomic analyses reveal stress adaptation of pistachio i
206 Our integrated
genomic analyses reveal that H2A.Z.2 controls the transc
207 Genomic analyses reveal that macroH2A1 and macroH2A2, to
208 Comparative
genomic analyses reveal that most of the SHP cistrome, i
209 Comparative population
genomic analyses reveal that pistachio was domesticated
210 Genomic analyses reveal that signature genetic lesions i
211 Our in vitro transcription and
genomic analyses reveal that the NRPD1 N-terminus is cri
212 Genomic analyses reveal that up 1.7% of all identified h
213 Overall, comparative and
genomic analyses reveal the emergence of a new group or
214 Population
genomic analyses reveal the evolutionary history of Citr
215 Genomic analyses revealed (11) prevalence of strains fro
216 Integrated
genomic analyses revealed a miRNA-regulatory network tha
217 Genomic analyses revealed a putative chemoreceptor-encod
218 Further phylogenetic and population
genomic analyses revealed extensive loss of genetic dive
219 Genomic analyses revealed genes and pathways that associ
220 Comparative
genomic analyses revealed high similarities between the
221 Population
genomic analyses revealed microdiversity within bacteria
222 Our
genomic analyses revealed multiple independent duplicati
223 Here, comparative
genomic analyses revealed that a local duplication of an
224 Genomic analyses revealed that all clones in polyclonal
225 Genomic analyses revealed that Hnf4a directly regulates
226 Recent
genomic analyses revealed that the coding regions of PbA
227 Evolutionary
genomic analyses revealed that these isolates belong to
228 Genomic analyses revealed that three Yellowstone Lake ph
229 us is still obscure, our previous functional
genomics analyses revealed a correlation between the let
230 Here, we set out how
genomic analyses should be used during an epidemic and p
231 Mass spectrometry, biochemical and
genomic analyses show co-existence of the H3K23ac and H3
232 Our molecular population
genomic analyses show higher deletion than insertion mut
233 Various
genomic analyses show that all examined humans are homoz
234 Genomic analyses show that major QTL control these trait
235 Genomic analyses show that Perkinsela sp. has lost the a
236 Comparative
genomic analyses show that the genome of M. purpureus is
237 Genomic analyses showed four gene segments in the viruse
238 Genomic analyses showed that certain species are specifi
239 Further functional
genomic analyses showed that eSTRs are enriched in conse
240 es were recovered from gulls in Iceland, and
genomic analyses showed that the viruses were geneticall
241 Population
genomic analyses showed that, whereas the majority of hu
242 Functional
genomic analyses subsequently demonstrated that affected
243 discussed, since it underlies all secondary
genomic analyses such as RNA sequencing (RNA-Seq), chrom
244 Solid tumors present several challenges for
genomic analyses,
such as tumor heterogeneity and tumor
245 Genomic analyses suggest an average window of over three
246 Comparative structural and
genomic analyses suggest that nonenveloped archaeal viru
247 Recent
genomic analyses suggest that promoter-promoter interact
248 s of pathogenic fungi and bacteria; however,
genomic analyses suggest that the majority of microbial
249 Phylogenetic and comparative
genomic analyses suggest that the structures have arisen
250 Moreover, population
genomic analyses suggested that many genes of small effe
251 Integrative
genomic analyses suggested that the aberrant expression
252 Epidemiological and
genomic analyses suggested that the anaconda juveniles a
253 Comparative
genomic analyses suggested that the original ACE1 cluste
254 Genetic and
genomic analyses support the conclusion that these effec
255 Our comparative
genomics analyses support this finding, showing that the
256 Prompted by recent
genomic analyses that identified cyclin E1 (CCNE1) gene
257 de association studies and other large-scale
genomic analyses that require robust, high-accuracy geno
258 Here we demonstrate, by both biochemical and
genomic analyses,
that MeCP2 directly interacts with nuc
259 As we expand the breadth and depth of
genomic analyses,
the biological and clinical complexity
260 Coupled with
genomic analyses,
these results point to sporulation as
261 hen used in systems genetics and integrative
genomics analyses,
these populations efficiently harness
262 Our integrative
genomic analyses thus show that it is possible to connec
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 gy and evolutionary history into comparative
genomic analyses to elucidate how P. syringae subverts t
269 quencing, we use phylogenomic and population
genomic analyses to establish species relationships.
270 Here we use comprehensive genetic and
genomic analyses to follow muscle development in a mouse
271 Yet the potential for
genomic analyses to guide local policy and community-bas
272 functional genetic screens and comprehensive
genomic analyses to identify CDK6 as a GBM oncogene that
273 Here, we have performed comparative
genomic analyses to identify the conserved sites of WDR5
274 dentifies candidate RiPP precursors with pan-
genomic analyses to identify which of these are encoded
275 g and integrated phylogenomic and population
genomic analyses to study hybridization and reconstruct
276 the white shark and comparative evolutionary
genomic analyses to the chondrichthyans, whale shark (El
277 rs of magnitude faster turnaround for common
genomic analyses,
transforming long-running batch jobs s
278 Comparative
genomic analyses uncovered evolutionarily conserved cons
279 Genomic analyses uncovered four distinct genes that allo
280 an database are on par with population-based
genomic analyses used in TCGA.
281 Genomic analyses using RNA-seq and ER ChIP-seq demonstra
282 In contrast with previous
genomic analyses using ~50x depth, deep sequencing allow
283 Comparative
genomic analyses utilizing a gene-independent whole-geno
284 Genomic analyses validate established evolutionary relat
285 Using comparative
genomic analyses,
we examined complete mitochondrial gen
286 imprinted gene network (IGN) into functional
genomic analyses,
we found that H19 mediates suppression
287 Using comparative
genomic analyses,
we identified genes unique to L. lacti
288 combination of phylogenetic and comparative
genomic analyses,
we then investigated the evolution of
289 Using complementary
genomics analyses,
we identified the interferon pathway
290 Population
genomic analyses were done with a hierarchical gene-by-g
291 Genomic analyses were performed using haplotype sharing
292 embers, phylogenetic and several comparative
genomics analyses were performed.
293 Comprehensive bioinformatics and functional
genomics analyses were used to identify key regulators,
294 lysis provides additional information beyond
genomic analyses,
which can improve understanding of can
295 Genomic analyses (
whole genome, exome, and transcriptome
296 trophysiological, molecular, and integrative
genomic analyses with focus on schizophrenia-relevant pa
297 uces a high cellular yield for cytologic and
genomic analyses with minimal risk of extraocular dissem
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