ライフサイエンスコーパス: chromatin immunoprecipitation sequencing

1 irmed by complementary approaches, including chromatin immunoprecipitation sequencing.

2 rine B cells and LPS-derived plasmablasts by chromatin immunoprecipitation sequencing.

3 immune precipitation-based methods, such as chromatin immunoprecipitation-sequencing.

4 egulatory elements by performing RNA-seq and chromatin immunoprecipitation-sequencing against H3 lysi

5 Chromatin immunoprecipitation sequencing analyses identi

6 Chromatin immunoprecipitation sequencing analyses reveal

7 Native chromatin immunoprecipitation sequencing analyses show t

8 RNA sequencing, and chromatin immunoprecipitation sequencing analyses show t

9 mRNA and chromatin immunoprecipitation sequencing analyses showed

10 Chromatin immunoprecipitation sequencing analyses showed

11 In addition, chromatin immunoprecipitation sequencing analyses showed

12 Gene profiling and chromatin immunoprecipitation sequencing analyses unrave

13 Chromatin immunoprecipitation-sequencing analyses of hum

14 Stage-specific global chromatin immunoprecipitation -sequencing analysis of th

15 We performed chromatin immunoprecipitation sequencing analysis and id

16 Chromatin immunoprecipitation sequencing analysis and tr

17 ed acetylation is loaded onto chromatin, and chromatin immunoprecipitation sequencing analysis demons

18 Combined RNA and chromatin immunoprecipitation sequencing analysis demons

19 We performed Sp7 chromatin immunoprecipitation sequencing analysis identi

20 Using in vivo chromatin immunoprecipitation sequencing analysis in rat

21 Chromatin immunoprecipitation sequencing analysis of the

22 Chromatin immunoprecipitation sequencing analysis reveal

23 Chromatin immunoprecipitation sequencing analysis reveal

24 Chromatin immunoprecipitation sequencing analysis sugges

25 ic targets in CIC-DUX4 sarcoma, we performed chromatin immunoprecipitation sequencing analysis using

26 Chromatin immunoprecipitation sequencing analysis with i

27 ese to concurrent RNA-sequencing and H3K27ac chromatin immunoprecipitation sequencing analysis.

28 ites) within the human genome as assessed by chromatin immunoprecipitation sequencing analysis.

29 Chromatin immunoprecipitation-sequencing analysis indica

30 RNA- and chromatin immunoprecipitation-sequencing analysis of H3K

31 Chromatin immunoprecipitation-sequencing analysis of Isl

32 Transcriptome and chromatin immunoprecipitation-sequencing analysis provid

33 Furthermore, chromatin immunoprecipitation-sequencing analysis reveal

34 Genome-wide chromatin immunoprecipitation-sequencing analysis reveal

35 s determined by RNA-sequencing combined with chromatin immunoprecipitation-sequencing analysis reveal

36 -expressing human bladder cancer cells by AR chromatin immunoprecipitation sequencing and complementa

37 V5-tagged PML::RARA, using anti-V5-PML::RARA chromatin immunoprecipitation sequencing and CUT&RUN app

38 inding as well as H3 lysine 4 trimethylation chromatin immunoprecipitation sequencing and gene expres

39 Chromatin immunoprecipitation sequencing and gene expres

40 Chromatin immunoprecipitation sequencing and gene expres

41 Using chromatin immunoprecipitation sequencing and Hi-C 3.0 in

42 Chromatin immunoprecipitation sequencing and immunopreci

43 Using chromatin immunoprecipitation sequencing and luciferase

44 Chromatin immunoprecipitation sequencing and methylation

45 Using a combination of chromatin immunoprecipitation sequencing and microarray

46 Our distribution was supported by chromatin immunoprecipitation sequencing and microarray

47 mapping of these processes in large scale by chromatin immunoprecipitation sequencing and other metho

48 d a combination of genetics, RNA sequencing, chromatin immunoprecipitation sequencing and phenotypic

49 Quantitative chromatin immunoprecipitation sequencing and promoter re

50 Utilizing chromatin immunoprecipitation sequencing and RNA sequenc

51 ine-capture technique that was combined with chromatin immunoprecipitation sequencing and RNA sequenc

52 Chromatin immunoprecipitation sequencing and RNA sequenc

53 We used chromatin immunoprecipitation sequencing and RNA sequenc

54 utilized bioinformatic approaches, including chromatin immunoprecipitation sequencing and RNA-Seq, to

55 Chromatin immunoprecipitation sequencing and RNA-sequenc

56 Chromatin immunoprecipitation sequencing and RNA-sequenc

57 egulates adult neural stem cells, we perform chromatin immunoprecipitation sequencing and RNA-sequenc

58 Dynamic chromatin immunoprecipitation sequencing and self-transc

59 pathway, ETHYLENE INSENSITIVE3 (EIN3), using chromatin immunoprecipitation sequencing and transcript

60 -inducible isogenic cell lines and performed chromatin immunoprecipitation sequencing and transcripto

61 ity on the NKX2-5 enhancer was studied using chromatin immunoprecipitation sequencing and transposase

62 uced genes were identified by integration of chromatin immunoprecipitation-sequencing and RNA-sequenc

63 t approaches for the study of the epigenome (chromatin immunoprecipitation sequencing) and transcript

64 these activities, we applied RNA sequencing, chromatin immunoprecipitation sequencing, and assay for

65 s in Arabidopsis seedlings were generated by chromatin immunoprecipitation sequencing, and changes in

66 cing, genome-wide RNA polymerase II (RNPII), chromatin immunoprecipitation sequencing, and DNase sequ

67 ration of whole-genome bisulfite sequencing, chromatin immunoprecipitation sequencing, and RNA sequen

68 ncluded genetically modified cell lines, RNA/chromatin immunoprecipitation sequencing, and single-cel

69 ted and analyzed by RNA sequencing, H3K27me3 chromatin immunoprecipitation sequencing, and sonication

70 tion RNA sequencing, methylation sequencing, chromatin immunoprecipitation sequencing, and whole-geno

71 nalysis in combination with ATAC-sequencing, chromatin immunoprecipitation-sequencing, and reporter g

72 ints using an acetylated histone H3 lysine 9 chromatin immunoprecipitation sequencing approach reveal

73 udy combining phenotypic, transcriptomic and chromatin immunoprecipitation sequencing approaches iden

74 Biochemical, structural and integrated chromatin immunoprecipitation-sequencing-based analyses

75 Transcriptome and chromatin immunoprecipitation sequencing (ChIP-seq) anal

76 Chromatin immunoprecipitation sequencing (ChIP-seq) anal

77 of FXR in healthy and dietary obese mice by chromatin immunoprecipitation sequencing (ChIP-seq) anal

78 phorylation, mass spectrometry analysis, and chromatin immunoprecipitation sequencing (ChIP-seq) anal

79 Bioinformatic and chromatin immunoprecipitation sequencing (ChIP-seq) anal

80 SA2 binding and R-loops sites extracted from Chromatin Immunoprecipitation sequencing (ChIP-seq) and

81 We combined Pol II chromatin immunoprecipitation sequencing (ChIP-seq) and

82 Combining gene targeting with chromatin immunoprecipitation sequencing (ChIP-seq) and

83 Chromatin immunoprecipitation sequencing (ChIP-seq) and

84 ) assays, transient expression analysis, and Chromatin Immunoprecipitation sequencing (ChIP-seq) assa

85 Using chromatin immunoprecipitation sequencing (ChIP-seq) comb

86 tory cells, and a publically available STAT3 chromatin immunoprecipitation sequencing (ChIP-Seq) data

87 Methods for the analysis of chromatin immunoprecipitation sequencing (ChIP-seq) data

88 Analysis of chromatin immunoprecipitation sequencing (ChIP-Seq) data

89 on overlap analysis of transcription factor chromatin immunoprecipitation sequencing (ChIP-seq) data

90 To train our EPBDxDNABERT-2, we used chromatin immunoprecipitation sequencing (ChIP-Seq) data

91 Chromatin immunoprecipitation sequencing (ChIP-seq) expe

92 Chromatin immunoprecipitation sequencing (ChIP-Seq) expe

93 Chromatin immunoprecipitation sequencing (ChIP-seq) expe

94 Here, we combined chromatin immunoprecipitation sequencing (ChIP-seq) for

95 use basal ganglia development, we integrated chromatin immunoprecipitation sequencing (ChIP-seq) for

96 e report the genomic landscape of REC8 using chromatin immunoprecipitation sequencing (ChIP-seq) in A

97 Our genome wide approach by chromatin immunoprecipitation sequencing (ChIP-seq) in h

98 Genome-wide chromatin immunoprecipitation sequencing (ChIP-seq) in w

99 Chromatin immunoprecipitation sequencing (ChIP-seq) is a

100 iction of gene expression from polymerase II chromatin immunoprecipitation sequencing (ChIP-seq) meas

101 ociation study (HAWAS) by performing H3K27ac chromatin immunoprecipitation sequencing (ChIP-seq) on 2

102 Using chromatin immunoprecipitation sequencing (ChIP-seq) on p

103 assessed using specific antibody pulldown in Chromatin Immunoprecipitation Sequencing (ChIP-Seq) or C

104 measured and inferred motifs are enriched in chromatin immunoprecipitation sequencing (ChIP-seq) peak

105 Using simulated reads, RNA-seq reads and chromatin immunoprecipitation sequencing (ChIP-seq) read

106 Here we report a chromatin immunoprecipitation sequencing (ChIP-seq) reso

107 Huang et al. (2013) recently reported that chromatin immunoprecipitation sequencing (ChIP-seq) reve

108 Chromatin immunoprecipitation sequencing (ChIP-seq) reve

109 Chromatin immunoprecipitation sequencing (ChIP-seq) reve

110 Chromatin immunoprecipitation sequencing (ChIP-Seq) show

111 Chromatin immunoprecipitation sequencing (ChIP-seq) show

112 Chromatin immunoprecipitation sequencing (ChIP-seq) show

113 ntary DNA ends sequencing (5' RACE-Seq), and chromatin immunoprecipitation sequencing (ChIP-Seq) show

114 Chromatin immunoprecipitation sequencing (ChIP-seq) stud

115 Chromatin immunoprecipitation sequencing (ChIP-seq) stud

116 Here, we used chromatin immunoprecipitation sequencing (ChIP-seq) tech

117 level of transcriptional regulation, we used chromatin immunoprecipitation sequencing (ChIP-Seq) to e

118 e use transcriptome sequencing (RNA-seq) and chromatin immunoprecipitation sequencing (ChIP-seq) to i

119 Here, we use chromatin immunoprecipitation sequencing (ChIP-seq) to s

120 onad development among species, we performed chromatin immunoprecipitation sequencing (ChIP-seq) usin

121 By comparing TOP1 occupancy using chromatin immunoprecipitation sequencing (ChIP-seq) vers

122 Using chromatin immunoprecipitation sequencing (ChIP-Seq) we r

123 Gene expression analysis and chromatin immunoprecipitation sequencing (ChIP-seq) were

124 Here, we integrate EBNA1 chromatin immunoprecipitation sequencing (ChIP-Seq) with

125 Chromatin immunoprecipitation sequencing (ChIP-seq), a m

126 mics by performing RNA sequencing (RNA-seq), chromatin immunoprecipitation sequencing (ChIP-seq), and

127 By integration of transcriptome, chromatin immunoprecipitation sequencing (CHIP-seq), Ass

128 Integrative analysis of chromatin immunoprecipitation sequencing (ChIP-seq), ass

129 We further used chromatin immunoprecipitation sequencing (ChIP-seq), bul

130 alyses of R-loop data with existing RNA-seq, chromatin immunoprecipitation sequencing (ChIP-seq), DNa

131 tu mapping RNA-genome interactions (iMARGI), chromatin immunoprecipitation sequencing (ChIP-seq), HiC

132 he cytokinin primary response, making use of chromatin immunoprecipitation sequencing (ChIP-seq), pro

133 ponential enrichment sequencing (SELEX-seq), chromatin immunoprecipitation sequencing (ChIP-seq), RNA

134 Here, using chromatin immunoprecipitation sequencing (ChIP-seq), we

135 Using chromatin immunoprecipitation sequencing (ChIP-seq), we

136 enome wide in the HNSCC model UM-SCC46 using chromatin immunoprecipitation sequencing (ChIP-seq).

137 etected by existing computational methods or chromatin immunoprecipitation sequencing (ChIP-seq).

138 e confirm these hypotheses using genome-wide chromatin immunoprecipitation sequencing (ChIP-Seq).

139 s likely functionally relevant, validated by chromatin immunoprecipitation sequencing (ChIP-seq).

140 ell as data from related experiments such as Chromatin Immunoprecipitation sequencing (ChIP-Seq).

141 st, inexpensive, and more easily scaled than chromatin immunoprecipitation sequencing (ChIP-seq).

142 On the basis of in vivo KLF4 chromatin immunoprecipitation-sequencing (ChIP-seq) anal

143 However, most chromatin immunoprecipitation-sequencing (ChIP-seq) anal

144 entation of Wnt target genes was detected in chromatin immunoprecipitation-sequencing (ChIP-seq) and

145 Using chromatin immunoprecipitation-sequencing (ChIP-seq) and

146 Nuc-MS is highly concordant with chromatin immunoprecipitation-sequencing (ChIP-seq) and

147 of STAT1 and STAT3 using genetic models and chromatin immunoprecipitation-sequencing (ChIP-seq) appr

148 ontrol and desiccation stress conditions via chromatin immunoprecipitation-sequencing (ChIP-seq) appr

149 Chromatin immunoprecipitation-sequencing (ChIP-seq) assa

150 regions via studying several published PHF8 chromatin immunoprecipitation-sequencing (ChIP-Seq) data

151 Chromatin immunoprecipitation-sequencing (ChIP-seq) data

152 Chromatin immunoprecipitation-sequencing (ChIP-seq) demo

153 other parameters influence interpretation of chromatin immunoprecipitation-sequencing (ChIP-seq) expe

154 The method can be used in parallel with chromatin immunoprecipitation-sequencing (ChIP-seq) expe

155 Finally, using chromatin immunoprecipitation-sequencing (ChIP-seq) of D

156 Transcriptomics and chromatin immunoprecipitation-sequencing (ChIP-seq) of I

157 Here, we use chromatin immunoprecipitation-sequencing (ChIP-seq) of t

158 Chromatin ImmunoPrecipitation-Sequencing (ChIP-Seq) peak

159 for continuous functional genomic data (e.g. chromatin immunoprecipitation-sequencing (ChIP-seq) peak

160 inally, whereas RNA-sequencing (RNA-seq) and chromatin immunoprecipitation-sequencing (ChIP-seq) show

161 chromatin enriched with an FXR antibody and chromatin immunoprecipitation-sequencing (ChIP-seq) to e

162 The method combines deep, long-read chromatin immunoprecipitation-sequencing (ChIP-seq) with

163 Here, using a combination of chromatin immunoprecipitation-sequencing (ChIP-seq), mic

164 HilD across the S. Typhimurium genome using chromatin immunoprecipitation-sequencing (ChIP-seq).

165 d de novo using epigenetic data derived from chromatin immunoprecipitation-sequencing (ChIP-Seq).

166 By analyzing CREB genomic occupancy from chromatin-immunoprecipitation sequencing (ChIP-seq) data

167 is allows us to efficiently compare numerous chromatin-immunoprecipitation sequencing (ChIP-seq) data

168 cing data after TCF7L2 knockdown with TCF7L2 chromatin-immunoprecipitation sequencing (ChIP-seq) data

169 Chromatin-immunoprecipitation-sequencing (ChIP-seq)-repo

170 sion (transcriptome sequencing [RNA-seq] and chromatin immunoprecipitation sequencing [ChIP-seq]).

171 now report the successful adaptation of this chromatin immunoprecipitation sequencing (ChIPseq) appro

172 Using chromatin immunoprecipitation sequencing combined with g

173 Chromatin immunoprecipitation sequencing confirmed that

174 g of FOXA3 to target genes was identified by chromatin immunoprecipitation sequencing correlated with

175 In chromatin immunoprecipitation sequencing, cyclin D1 occu

176 The chromatin immunoprecipitation sequencing data are availa

177 Chromatin immunoprecipitation sequencing data collected

178 /CDK kinase inhibition previously described, chromatin immunoprecipitation sequencing data combined w

179 ted analysis of transcriptomic profiling and chromatin immunoprecipitation sequencing data demonstrat

180 Bioinformatics analysis of ENCODE chromatin immunoprecipitation sequencing data from cell

181 these findings to human disease, analysis of chromatin immunoprecipitation sequencing data revealed t

182 Integration of BAT RNA sequencing and chromatin immunoprecipitation sequencing data revealed t

183 shed Arabidopsis (Arabidopsis thaliana) EIN3 chromatin immunoprecipitation sequencing data set, we in

184 Analysis of chromatin immunoprecipitation sequencing data sets for M

185 integrated these profiles with whole-animal chromatin immunoprecipitation sequencing data to deconvo

186 the identified CNSs were evaluated using TF chromatin immunoprecipitation sequencing data, resulting

187 augmented with matched whole-genome, RNA and chromatin immunoprecipitation sequencing data.

188 ds/degradome reads, RNA sequencing, and even chromatin immunoprecipitation sequencing data; it also p

189 KANSL1 and H4K8 chromatin immunoprecipitation-sequencing data demonstrat

190 Comparison with chromatin immunoprecipitation-sequencing data implies th

191 iGene multiplex assay and publicly-available chromatin immunoprecipitation-sequencing data.

192 Moreover, analysis of ChIP-seq (chromatin immunoprecipitation sequencing) data revealed

193 Chromatin immunoprecipitation sequencing database querie

194 gnaling node perturbation transcriptomic and chromatin immunoprecipitation-sequencing datasets.

195 ns and present a simple workflow for mapping chromatin immunoprecipitation-sequencing datasets.

196 throughput sequencing data, such as RNA-seq, chromatin immunoprecipitation sequencing, DNA-seq, etc.

197 Significance: Plasma cell-free chromatin immunoprecipitation sequencing enables phenoty

198 andibular salivary gland (SMG) by performing chromatin immunoprecipitation sequencing experiments for

199 Recently, many chromatin immunoprecipitation sequencing experiments hav

200 Genome-wide chromatin immunoprecipitation sequencing experiments rev

201 Using RNA-sequencing and chromatin immunoprecipitation sequencing experiments, we

202 ined using data from multiple PAX8 and H3K27 chromatin immunoprecipitation sequencing experiments.

203 Chromatin immunoprecipitation-sequencing experiments fol

204 lved in AVM formation, we performed RNA- and chromatin immunoprecipitation-sequencing experiments on

205 nds by exponential enrichment) and ChIP-seq (chromatin immunoprecipitation-sequencing) experiments.

206 Chromatin immunoprecipitation sequencing facilitated the

207 Here we describe fixed-tissue chromatin immunoprecipitation sequencing (FiT-seq), a me

208 ole for CLOCK in human neurons by performing chromatin immunoprecipitation sequencing for endogenous

209 al genomics methodology to interrogate human chromatin immunoprecipitation-sequencing, genome-wide as

210 Chromatin immunoprecipitation sequencing identified CLOC

211 Chromatin immunoprecipitation sequencing illustrates tha

212 We studied CTCF binding by chromatin immunoprecipitation sequencing in cells from p

213 Chromatin immunoprecipitation sequencing in chick limb b

214 lk and single-cell RNA sequencing coupled to chromatin immunoprecipitation sequencing in hematopoieti

215 bal analysis of short capped RNAs and Pol II Chromatin Immunoprecipitation sequencing in MCF-7 breast

216 Here, using in vivo chromatin immunoprecipitation sequencing in mouse kidney

217 We used genome-wide chromatin immunoprecipitation sequencing in primary huma

218 Chromatin immunoprecipitation sequencing in T helper 17

219 Tcf1 chromatin immunoprecipitation sequencing in T(FH) cells

220 Chromatin immunoprecipitation sequencing in wild-type an

221 Chromatin immunoprecipitation-sequencing in lymphoblasto

222 Here, we use co-immunoprecipitation assays, chromatin immunoprecipitation sequencing, in silico meth

223 tured myofibroblasts by bulk-RNA sequencing, chromatin immunoprecipitation sequencing, metabolomics,

224 e accessible chromatin sequencing (n=6), and chromatin immunoprecipitation sequencing (n=6) for deter

225 AL1 oncogene, a finding validated in vivo by chromatin immunoprecipitation sequencing of a patient-de

226 ere analyzed by RNA sequencing (RNA-seq) and chromatin immunoprecipitation sequencing of acetylated h

227 We performed chromatin immunoprecipitation sequencing of CSCs to conf

228 Here, we used chromatin immunoprecipitation sequencing of dimethylated

229 hole-genome bisulfite sequencing and H3K27Ac chromatin-immunoprecipitation sequencing of primary tumo

230 We performed AR chromatin immunoprecipitation sequencing on primary pros

231 aCREs were defined by reanalysis of H3K27ac chromatin immunoprecipitation sequencing peaks in 25 neu

232 read datasets (166,058 previously unresolved chromatin immunoprecipitation sequencing peaks) to provi

233 We derived 27 328 chromatin immunoprecipitation-sequencing peaks for PPARg

234 sing both whole-transcriptome sequencing and chromatin immunoprecipitation sequencing pinpointed onco

235 Notably, in vitro RNA-sequencing and chromatin immunoprecipitation sequencing profiles identi

236 Chromatin immunoprecipitation sequencing profiling in En

237 PEP binding to chloroplast DNA using plastid chromatin immunoprecipitation-sequencing (ptChIP-seq).

238 Using simulated and chromatin immunoprecipitation sequencing reads, we defin

239 LMNA chromatin immunoprecipitation-sequencing, reduced repres

240 ar cell in vivo Transcriptome sequencing and chromatin immunoprecipitation sequencing results showed

241 is shared between inbred parents and matches chromatin immunoprecipitation sequencing results; and (3

242 Chromatin immunoprecipitation-sequencing results for sev

243 AIB1 4 chromatin immunoprecipitation sequencing revealed enhanc

244 Chromatin immunoprecipitation sequencing revealed H3K27m

245 RNA-sequencing and chromatin immunoprecipitation sequencing revealed HMGA1

246 Chromatin immunoprecipitation sequencing revealed reduce

247 Further, chromatin immunoprecipitation sequencing revealed that B

248 Chromatin immunoprecipitation sequencing revealed that i

249 ial genome-wide transcriptional profile with chromatin immunoprecipitation sequencing revealed that P

250 Furthermore, chromatin immunoprecipitation sequencing revealed that t

251 Chromatin immunoprecipitation sequencing revealed the tr

252 Chromatin immunoprecipitation-sequencing revealed bindin

253 Chromatin immunoprecipitation-sequencing revealed that B

254 Chromatin immunoprecipitation sequencing reveals 4785 p5

255 Gene expression analysis and chromatin immunoprecipitation sequencing reveals differe

256 Moreover, chromatin immunoprecipitation-sequencing reveals BRG1 bi

257 Chromatin immunoprecipitation-sequencing reveals that TF

258 Chromatin-immunoprecipitation-sequencing reveals that MY

259 site for a TF functional switch by employing chromatin immunoprecipitation sequencing, RNA expression

260 rioritized candidate SNPs were examined with chromatin immunoprecipitation sequencing, RNA sequencing

261 We also performed chromatin immunoprecipitation sequencing, RNA-sequencing

262 Furthermore, microarray and chromatin immunoprecipitation sequencing screens led to

263 Chromatin immunoprecipitation sequencing showed that a l

264 Chromatin immunoprecipitation sequencing showed that EIN

265 Chromatin immunoprecipitation sequencing showed that ERF

266 nt, genotype-dependent binding, and enhanced chromatin immunoprecipitation sequencing signal at AD ri

267 Chromatin immunoprecipitation sequencing studies identif

268 e in migration, and combined snATAC-seq with chromatin immunoprecipitation sequencing studies suggest

269 g of Dmrt6 mutant testes together with DMRT6 chromatin immunoprecipitation sequencing suggest that DM

270 a transcriptional regulator, we performeded chromatin immunoprecipitation-sequencing targeting ZBTB1

271 ng on the integration of DNA methylation and chromatin immunoprecipitation-sequencing technologies in

272 Here, we show by chromatin immunoprecipitation-sequencing that OBF1 exten

273 ylation regulates MeCP2 function and show by chromatin immunoprecipitation-sequencing that this modif

274 We used RNA sequencing coupled with chromatin immunoprecipitation sequencing to identify gen

275 We used high-resolution chromatin immunoprecipitation sequencing to identify the

276 Here, we used chromatin immunoprecipitation sequencing to map the geno

277 because H3K56ac combines with NSO factors in chromatin immunoprecipitation sequencing to mark the reg

278 We used chromatin immunoprecipitation-sequencing to identify 406

279 We conducted chromatin immunoprecipitation-sequencing to map SRF-bind

280 ome-wide LRH-1-binding sites using ChIP-seq (chromatin immunoprecipitation sequencing), uncovering pr

281 To define the pS118-ER cistrome, chromatin immunoprecipitation sequencing was performed o

282 e-wide mapping of FOXA2 binding intervals by chromatin immunoprecipitation sequencing was performed u

283 ERbeta regulates different classes of genes, chromatin immunoprecipitation-sequencing was performed t

284 th high-throughput sequencing (ATAC-seq) and chromatin immunoprecipitation sequencing we identified e

285 Using chromatin immunoprecipitation sequencing, we demonstrate

286 Using chromatin immunoprecipitation sequencing, we identified

287 ns and 13C-tracing, polysomal profiling, and chromatin immunoprecipitation sequencing, we identified

288 rmediate, and poised enhancers determined by chromatin immunoprecipitation-sequencing, with parallel