ライフサイエンスコーパス: bisulfite sequencing

1 served in assays such as ChIP Sequencing and bisulfite sequencing.

2 DNMT3L, shown by knockdown assays and sodium bisulfite sequencing.

3 y the pattern of CpG methylation revealed by bisulfite sequencing.

4 ylation to nearby CpG sites, shown by sodium bisulfite sequencing.

5 g half of each male's semen for whole genome bisulfite sequencing.

6 m HumanMethylation450 array and whole genome bisulfite sequencing.

7 ATAC sequencing and single-cell whole-genome bisulfite sequencing.

8 ation landscape, as assessed by whole-genome bisulfite sequencing.

9 ulfite sequencing and reduced representation bisulfite sequencing.

10 Array findings were validated by bisulfite sequencing.

11 s of genomic DNA followed by next generation bisulfite sequencing.

12 uman aorta sample using whole-genome shotgun bisulfite sequencing.

13 idated using enhanced reduced representation bisulfite sequencing.

14 er hypermethylation of ULK2 was confirmed by bisulfite sequencing.

15 ared with control heifers using whole-genome bisulfite sequencing.

16 d can be quantified at base resolution using bisulfite sequencing.

17 CpGs that previously cannot be predicted by bisulfite sequencing.

18 tion occurred for monocytes for both RNA and bisulfite sequencing.

19 in parents and offspring using whole-genome bisulfite sequencing.

20 or Infinium microarrays and various types of bisulfite sequencing.

21 Here, we present 4mC-Tet-assisted bisulfite-sequencing (4mC-TAB-seq), a next-generation se

22 Bisulfite sequencing allows base-pair resolution profili

23 By bisulfite sequencing analysis of auditory forebrain DNA,

24 ecipitation, luciferase promoter assays, and bisulfite sequencing analysis of sites in proximity.

25 Bisulfite sequencing analysis revealed the premature pro

26 Integration of single-cell bisulfite sequencing analysis with single-cell transcrip

27 trained on 14 tissues with both whole genome bisulfite sequencing and 450K array data.

28 pecific CpG region in 9 colorectal tumors by bisulfite sequencing and apply a tumor development model

29 enetic mark, was investigated using targeted bisulfite sequencing and characterized at functional lev

30 elopment in NeuN+ neurons using whole-genome bisulfite sequencing and compare them to non-neurons (pr

31 genome-wide, we used reduced representation bisulfite sequencing and found an extensive reorganizati

32 Whole-genome bisulfite sequencing and H3K27Ac chromatin-immunoprecipi

33 ompares favorably with nucleotide-resolution bisulfite sequencing and has better predictive power wit

34 Low-coverage whole-genome bisulfite sequencing and high-coverage sequence-capture

35 lastic leukemias (B-ALLs) using whole-genome bisulfite sequencing and high-definition microarrays, al

36 MM), a plasma cell neoplasm, by whole-genome bisulfite sequencing and high-density arrays, we observe

37 cell differentiation program by whole-genome bisulfite sequencing and high-density microarrays.

38 Short-read bisulfite sequencing and long-read PacBio sequencing hav

39 ation measurements confirmed by whole genome bisulfite sequencing and offers a better balance between

40 Study of whole-genome bisulfite sequencing and reduced representation bisulfit

41 olution through methods such as whole-genome bisulfite sequencing and reduced representation bisulfit

42 bisulfite sequencing, reduced representation bisulfite sequencing and RNA sequencing were performed o

43 re investigated using reduced representation bisulfite sequencing and RNA sequencing, respectively.

44 Using 17 whole-genome bisulfite sequencing and RNA-seq datasets from different

45 Reduced representation bisulfite sequencing and RNA-seq show that dCas9-SunTag-

46 examine promoter accessibility, we performed bisulfite sequencing and show that none of the MHC class

47 Here, through bisulfite sequencing and strand-specific mapping, we sho

48 counts from bisulfite sequencing, oxidative bisulfite sequencing and Tet-Assisted Bisulfite sequenci

49 region (-186 to -20), which was confirmed by bisulfite-sequencing and methylation-specific PCR (MSP)

50 oprecipitation with sequencing, whole-genome bisulfite sequencing, and chromosome conformation captur

51 We use whole genome bisulfite sequencing, and find that differentiation of m

52 efficient (R = 0.884) between our method and bisulfite sequencing, and for 92.0% of CpG sites, methyl

53 epigenome, replication-timing, whole-genome bisulfite sequencing, and gene expression profiles from

54 ipitation-sequencing, reduced representative bisulfite sequencing, and RNA-sequencing were performed

55 elity, we implemented a genome-scale hairpin bisulfite sequencing approach to generate methylation da

56 With the genome-scale hairpin bisulfite sequencing approach, we demonstrated that the

57 everal cost-effective reduced representation bisulfite sequencing approaches (RRBS) have been recentl

58 nt a method to map DNA methylation data from bisulfite sequencing approaches to CpG sites measured wi

59 lation modifications from any combination of bisulfite sequencing approaches, including reduced, oxid

60 using microarray, ChIP-seq, and whole-genome bisulfite sequencing approaches.

61 omplexes of DNMT3A and DNMT3B, and performed bisulfite sequencing-based single-turnover methylation a

62 nt of high-throughput sequencing technology, bisulfite-sequencing-based DNA methylation profiling met

63 bisulfite sequencing (RRBS) and whole genome bisulfite sequencing (bis-seq) opens the door to study D

64 ulfite sequencing and reduced representation bisulfite sequencing brings the availability of DNA meth

65 Bisulfite sequencing (BS-seq) has emerged recently as th

66 tially active gene regulatory sequences; and bisulfite sequencing (BS-seq) quantifies DNA methylation

67 We also performed whole genome bisulfite sequencing (BS-seq) to determine the biologica

68 In standard bisulfite sequencing (BS-seq), unmodified C, 5fC and 5ca

69 methylation signals with similar accuracy as bisulfite sequencing (BS-Seq; single nucleotide resoluti

70 g methyl-sensitive restriction digestion and bisulfite sequencing cannot distinguish between 5-mC and

71 lated methods such as nasBS-seq (nascent DNA bisulfite sequencing), ChIP-BS-seq (ChIP followed by bis

72 HSD11B2 and FKBP5 are seen in a minority of bisulfite sequencing clones, these epigenetic changes, a

73 replicate these findings using whole genome bisulfite sequencing, comparing epidermis from an additi

74 Bisulfite sequencing confirmed dense promoter hypermethy

75 Bisulfite sequencing confirmed hypermethylation of the A

76 genes was analyzed using 450K Beadchips and bisulfite sequencing; correlations between maternal and

77 we present customised Reduced Representation Bisulfite Sequencing (cuRRBS), a novel and easy-to-use c

78 Whole-genome bisulfite sequencing currently provides the highest-prec

79 ient and convenient tool for high-throughput bisulfite sequencing data analysis that can be broadly u

80 nderstand relationships between whole-genome bisulfite sequencing data and expression.

81 GE properly accounts for the count nature of bisulfite sequencing data and incorporates allele-specif

82 terns with those from Reduced Representation Bisulfite Sequencing data and through comparison with pr

83 we reanalyzed K562 RNA-seq and whole-genome bisulfite sequencing data for allele-specific expression

84 We generate whole-genome bisulfite sequencing data for approximately 30 adipose a

85 nalysis of previously published whole-genome bisulfite sequencing data for intragonadal PGCs.

86 I 0.91-0.98) from the reduced representation bisulfite sequencing data from 35 whole blood samples.

87 Reduced representation bisulfite sequencing data from sperm of rats exposed to

88 We generated bisulfite sequencing data from two tissues of Brachypodi

89 By analyzing whole-genome bisulfite sequencing data in a phylogenetic context, it

90 ute deviations support the validity of using bisulfite sequencing data in combination with Illumina b

91 Bisulfite sequencing data indicate that active nucleolar

92 Here, we use whole-genome bisulfite sequencing data on two highly divergent mouse

93 d validation with 101 reduced-representation bisulfite sequencing data sets and 637 methylation array

94 pe blocks, after analysis of 61 whole-genome bisulfite sequencing data sets and validation with 101 r

95 ion sequencing (MeDIP-seq), and whole-genome bisulfite sequencing data to generate and orthogonally v

96 Analysis of bisulfite sequencing data usually requires two tasks: to

97 d coverage depth in the case of whole-genome bisulfite sequencing data).

98 h results correlating well with whole genome bisulfite sequencing data, and demonstrate that human DN

99 tus and DNA polymorphisms, from whole-genome bisulfite sequencing data, and nucleosome occupancy from

100 dreds of transcription factors, whole-genome bisulfite sequencing data, ChIA-PET data, and functional

101 on analysis of DNA methylation patterns from bisulfite sequencing data, including the detection of re

102 Using high resolution hairpin oxidative bisulfite sequencing data, we precisely determine the am

103 vel CpG methylation patterns in whole genome bisulfite sequencing data.

104 odification assisted, and methylase-assisted bisulfite sequencing data.

105 entify bipolar methylated genomic regions in bisulfite sequencing data.

106 arrying out such analysis on high-throughput bisulfite sequencing data.

107 on studies have generated massive amounts of bisulfite sequencing data.

108 ware package for detecting mCs and DMRs from bisulfite sequencing data.

109 a mixture of binomial model to characterize bisulfite-sequencing data, and based on the model, we pr

110 dealing with the various sources of noise in bisulfite-sequencing data.

111 By utilizing a real bisulfite sequencing dataset generated from prostate can

112 o increase coverage of existing whole genome bisulfite sequencing datasets by imputing CpG methylatio

113 re, we have analyzed 34 diverse whole-genome bisulfite sequencing datasets in human and identified 31

114 nalysis of both human and mouse whole genome bisulfite sequencing datasets reveals read-level signatu

115 ally methylated regions from high-throughput bisulfite sequencing datasets, DMRfinder is the first th

116 present a set of preprocessing pipelines for bisulfite sequencing DNA methylation data that include a

117 Bisulfite sequencing evaluated DNA methylation of placen

118 The analysis of multiple whole-genome bisulfite sequencing experiments is supported, while mai

119 lyses of datasets from RNA-Seq, ChIP-Seq and bisulfite sequencing experiments.

120 gnment approach for processing the data from bisulfite sequencing experiments.

121 Furthermore, whole-genome bisulfite sequencing failed to reveal any evidence of de

122 Here, we used RNA bisulfite sequencing for transcriptome-wide quantitative

123 Here we used whole-genome bisulfite sequencing from 10 diverse human tissues to id

124 e information from whole genome and targeted bisulfite sequencing from 910 samples to perform genotyp

125 Bisulfite sequencing further reveals methylation of the

126 Bisulfite sequencing further shows that epigenetic repre

127 Conventional DNA bisulfite sequencing has been extended to single cell le

128 Bisulfite sequencing has been the gold standard for mapp

129 sulfite sequencing or reduced representation bisulfite sequencing) has become popular for studying hu

130 encing (RRBS) and hybrid selection (capture) bisulfite sequencing (HSBS).

131 We used whole-genome bisulfite sequencing in a mouse model with nonrandom XCI

132 ), a risky methylated gene, was confirmed by bisulfite sequencing in GBMs.

133 hlights the utility of low pass whole-genome bisulfite sequencing in identifying methylome variation

134 We examined DNA methylation by whole-genome bisulfite sequencing in neuronal and non-neuronal popula

135 tastable epialleles by performing genomewide bisulfite sequencing in peripheral blood lymphocyte (PBL

136 he human embryo and germ cells, and targeted bisulfite sequencing in term placentas.

137 s, publicly available reduced representation bisulfite sequencing in the human embryo and germ cells,

138 cers and promoters, genome-wide, by targeted bisulfite sequencing in two independent sample cohorts.

139 MSP and bisulfite sequencing indicated DNA demethylation of slug

140 Whole-genome bisulfite sequencing indicated that Dnmt3a and Dnmt3b pl

141 However, the standard workflow of bisulfite sequencing involves heat and strongly basic co

142 Bisulfite sequencing is a key methodology in epigenetics

143 Bisulfite sequencing is one of the most widely used tech

144 by the Illumina 450K array and whole genome bisulfite sequencing is still too expensive for many sam

145 methylation patterns in tissue whole genome bisulfite sequencing libraries reflect cell type.

146 dy, we describe low-input methylase-assisted bisulfite sequencing (liMAB-seq ) and single-cell MAB-se

147 ifications, including but not limited to RNA bisulfite sequencing, m(1)A-Seq, Par-CLIP, RIP-Seq, etc.

148 have recently developed a methylase-assisted bisulfite sequencing (MAB-seq) method that allows base-r

149 Here, we describe M.SssI methylase-assisted bisulfite sequencing (MAB-seq), a method that directly m

150 Study (MACHS) were profiled by whole-genome bisulfite sequencing (median coverage: [Formula: see tex

151 ular biology and optical approaches, such as bisulfite sequencing, microarrays, quantitative real-tim

152 ity within tumors, we performed genome-scale bisulfite sequencing of 104 primary chronic lymphocytic

153 Microarray-based screening and bisulfite sequencing of 20 nonmalignant and 29 PC tissue

154 ethylation states assessed from whole-genome bisulfite sequencing of 83 RILs uncovered widespread evi

155 ystem, we performed RNA-seq and whole-genome bisulfite sequencing of adult females and males from two

156 Whole-genome bisulfite sequencing of antigen-specific murine CD8 T ce

157 ying whole-exome sequencing and whole-genome bisulfite sequencing of cell free DNA (cfDNA) and of mat

158 ethylation profile of the same CpG-island by bisulfite sequencing of DNA obtained from blood of 34 FT

159 Bisulfite sequencing of exposed and control animals high

160 methylation is measured by deep whole-genome bisulfite sequencing of genomic DNA from tissues represe

161 nd hypothalamus) and methylome (whole-genome bisulfite sequencing of hypothalamus).

162 lower KLF4 and nitric oxide synthase 3, and bisulfite sequencing of KLF4 promoter identified a hyper

163 Using whole-genome bisulfite sequencing of normal B cell subsets, we observ

164 Whole-genome bisulfite sequencing of primary human naive, short-lived

165 to leukemogenesis, we performed whole-genome bisulfite sequencing of primary leukemic and non-leukemi

166 By employing a protocol for whole-genome bisulfite sequencing of single cells, we show that the l

167 Bisulfite sequencing of sperm DNA from conditioned F0 ma

168 We performed bisulfite sequencing on 23 CpG dinucleotides on the tran

169 nalysis, and enhanced reduced representation bisulfite sequencing on a cohort of paired diagnosis and

170 Other studies have performed whole-genome bisulfite sequencing on a few individuals, but these lac

171 We perform whole genome bisulfite sequencing on a set of unmatched samples inclu

172 To illustrate MCC-Seq, we use whole-genome bisulfite sequencing on adipose tissue (AT) samples and

173 in social insects, we performed whole-genome bisulfite sequencing on brains of the clonal raider ant

174 nd laser-capture microdissection followed by bisulfite sequencing on DNA isolated from prostate tissu

175 Asthma Study [n = 28]) was analyzed by using bisulfite sequencing or Illumina 450K arrays.

176 analyze DNA methylation data generated from bisulfite sequencing or Illumina methylation arrays.

177 by sequencing (BS-Seq, such as whole genome bisulfite sequencing or reduced representation bisulfite

178 sequencing cost in the case of whole-genome bisulfite sequencing, or from reduced resolution (inabil

179 mic DNA, we combined redBS-Seq and oxidative bisulfite sequencing (oxBS-Seq) to generate the first co

180 To this end, we have developed oxidative bisulfite sequencing (oxBS-seq), which can quantitativel

181 t a method to jointly model read counts from bisulfite sequencing, oxidative bisulfite sequencing and

182 Through whole-genome bisulfite sequencing paired with deep whole-genome and t

183 have developed BSPAT, a fast online tool for bisulfite sequencing pattern analysis.

184 ition, we validated the MeDIP-Seq results by bisulfite sequencing PCR (BSP) in some of the differenti

185 We performed bisulfite sequencing PCR of genomic DNA isolated from HB

186 s, RRBS, WGBS sequencing, and locus-specific bisulfite sequencing performed on the same human embryon

187 g of short reads by and high cost of current bisulfite sequencing platforms make them impractical for

188 However, analysis of data produced by bisulfite-sequencing poses statistical challenges owing

189 We adapted amplicon bisulfite-sequencing protocols to design IMPLICON for IC

190 Interestingly, additional RNA bisulfite sequencing provided first evidence for Dnmt2-m

191 Although Whole genome Bisulfite Sequencing provides high-quality methylation m

192 dative bisulfite sequencing and Tet-Assisted Bisulfite sequencing, providing simultaneous estimates o

193 Chromatin immunoprecipitation and bisulfite sequencing quantified epigenetic characteristi

194 an automated analysis toolkit for processing bisulfite sequencing reads.

195 Here we introduce reduced bisulfite sequencing (redBS-Seq), a quantitative method

196 biased omics profiling, such as whole genome bisulfite sequencing, reduced representation bisulfite s

197 deoxyuridine labeled nascent DNA followed by bisulfite sequencing (Repli-BS) measures post-replicatio

198 quencing and modified reduced representation bisulfite sequencing, respectively.

199 Bisulfite sequencing revealed aberrant hypermethylation

200 Bisulfite sequencing revealed no DNA-methylation in this

201 Bisulfite sequencing revealed that both human and mouse

202 Further Bisulfite sequencing revealed that miR-210 is embedded i

203 Locus-specific bisulfite sequencing revealed that the donor L1 and othe

204 Genome-wide DNA bisulfite sequencing revealed that the Tnf promoter was

205 Time-series whole genome bisulfite sequencing reveals extensive gain of CHH methy

206 te sequencing (WGBS), reduced representation bisulfite sequencing (RRBS) and hybrid selection (captur

207 Using both reduced representation bisulfite sequencing (RRBS) and microarray, we determine

208 g was performed using reduced representation bisulfite sequencing (RRBS) and RNA-sequencing (RNA-Seq)

209 e wide application of reduced representation bisulfite sequencing (RRBS) and whole genome bisulfite s

210 e apply our method to reduced representation bisulfite sequencing (RRBS) data from multiple regions o

211 Reduced representation bisulfite sequencing (RRBS) data was used to train an ep

212 raditional MspI-based Reduced Representation Bisulfite Sequencing (RRBS) protocol to all restriction

213 could be queried in a reduced representation bisulfite sequencing (RRBS) study of adult [Formula: see

214 We initially used reduced representation bisulfite sequencing (RRBS) to generate a methylome-wide

215 g mutated HTT, we use reduced representation bisulfite sequencing (RRBS) to map sites of DNA methylat

216 We used reduced representation bisulfite sequencing (RRBS) to profile DNA methylation i

217 and 450 K arrays) and reduced representation bisulfite sequencing (RRBS), only cover a small proporti

218 lation differences by reduced representation bisulfite sequencing (RRBS), we determined that, over ti

219 were identified using reduced representation bisulfite sequencing (RRBS).

220 uencing (RNA-Seq) and reduced-representation bisulfite sequencing (RRBS).

221 Here, we employed an enhanced version of bisulfite sequencing (RRBS/oxRRBS) followed by next gene

222 We report a single-cell bisulfite sequencing (scBS-seq) method that can be used

223 me maps from single cells, using single-cell bisulfite sequencing (scBS-seq), allowing the quantitati

224 ture with single-cell reduced representation bisulfite sequencing (scRRBS), to measure the CpG methyl

225 Targeted and whole-genome bisulfite sequencing showed that the induced ripening of

226 n patterns using single-cell, locus-specific bisulfite sequencing (SLBS).

227 Moreover, methylation-specific PCR and bisulfite sequencing studies revealed that TP73 promoter

228 Here, we have analyzed multiple bisulfite sequencing studies to address the methylation

229 encing studies, including RNA sequencing and bisulfite sequencing studies, are becoming increasingly

230 We also apply IMAGE to analyze two bisulfite sequencing studies, in which IMAGE identifies

231 e sequencing), ChIP-BS-seq (ChIP followed by bisulfite sequencing), TAB-seq, oxBS-seq, and fCAB-seq.

232 onic stem cells and show that, compared with bisulfite sequencing, TAPS results in higher mapping rat

233 The rapid emergence of bisulfite-sequencing technologies enables performing suc

234 we developed RBS-Seq, a modification of RNA bisulfite sequencing that enables the sensitive and simu

235 sign, particularly in reduced representation bisulfite sequencing, there is a need to develop more fl

236 ltiplexed single-cell reduced-representation bisulfite sequencing to B cells from healthy donors and

237 s hypothesis, we used reduced representation bisulfite sequencing to examine the cross-sectional geno

238 Using whole genome bisulfite sequencing to examine uncharted regions of the

239 Here we applied oxidative bisulfite sequencing to generate whole-genome DNA methyl

240 microdissection with reduced representation bisulfite sequencing to identify cancer-associated DNA m

241 we employed Enhanced Reduced Representation Bisulfite Sequencing to interrogate the epigenome of the

242 A recent study used genome-wide bisulfite sequencing to survey differences in DNA methyl

243 We used replicated bisulfite-sequencing to investigate patterns of DNA meth

244 Currently available bisulfite sequencing tools frequently suffer from low ma

245 on, DeepSignal achieves 90% correlation with bisulfite sequencing using just 20x coverage of reads, w

246 g (n = 12 per group), unbiased capture array bisulfite sequencing was combined with subsequent matrix

247 lation and hydroxymethylation with oxidative bisulfite sequencing was conducted and correlated with c

248 Whole-genome bisulfite sequencing was conducted to assess the dynamic

249 Reduced representation bisulfite sequencing was performed on DNA extracted from

250 Targeted bisulfite sequencing was performed with a subset of plac

251 Reduced representational bisulfite sequencing was then used to compare the differ

252 Finally, oxidative bisulfite sequencing was used to differentiate methylati

253 Whole-genome bisulfite sequencing was used to produce nucleotide reso

254 By using methylation-specific PCR and bisulfite sequencing we demonstrate that miR-663 promote

255 Using whole genome bisulfite sequencing we identified hundreds of different

256 Using targeted bisulfite sequencing, we examined methylation of 2100 ge

257 By performing genome-scale bisulfite sequencing, we find that DNMT3B-deficient iPSC

258 Here, using high-throughput bisulfite sequencing, we identified an APL-associated hy

259 Using whole-genome bisulfite sequencing, we show that crossover remodeling

260 Through whole-genome bisulfite sequencing, we showed that DNA methylation wen

261 Based on sequence capture bisulfite-sequencing, we find that CHH DNA methylation o

262 equencing and high-coverage sequence-capture bisulfite sequencing were applied to mutant lines to det

263 RNA-Seq and multiplex bisulfite sequencing were performed to examine gene expr

264 ne, AZA), methylation-specific PCR (MSP) and bisulfite sequencing were performed.

265 RNA sequencing and reduced representation bisulfite sequencing were used to create transcriptomic

266 tes sequencing (DNase-seq), and whole-genome bisulfite sequencing (WGBS or BS-seq) data revealed inte

267 Whole-genome bisulfite sequencing (WGBS) allows genome-wide DNA methy

268 hylation patterns comparable to whole-genome bisulfite sequencing (WGBS) along genes and regulatory e

269 Whole genome bisulfite sequencing (WGBS) also known as BS-seq has bee

270 Whole-genome bisulfite sequencing (WGBS) analyses of wild-type (WT) a

271 Whole-genome bisulfite sequencing (WGBS) analysis revealed that Tet-m

272 Here, we performed whole-genome bisulfite sequencing (WGBS) and RNA-sequencing (RNA-seq)

273 Whole-genome bisulfite sequencing (WGBS) and transcriptional profilin

274 Using sample-matched whole-genome bisulfite sequencing (WGBS) as a gold standard, we demon

275 ole-genome sequencing (WGS) and whole-genome bisulfite sequencing (WGBS) data on populations of moder

276 for detecting such events from whole-genome bisulfite sequencing (WGBS) data perform statistically i

277 oach to methylation analysis of whole genome bisulfite sequencing (WGBS) data permitted a high level

278 igenetic energy landscapes from whole-genome bisulfite sequencing (WGBS) data that enable us to quant

279 tematic comparisons of GPS with whole-genome bisulfite sequencing (WGBS) found that methylation diffe

280 Whole-genome bisulfite sequencing (WGBS) has been widely used to quan

281 Whole-genome bisulfite sequencing (WGBS) has emerged as the gold-stan

282 Whole-genome bisulfite sequencing (WGBS) is the gold standard for stu

283 Techniques like whole-genome bisulfite sequencing (WGBS) make it possible to determin

284 y process in A. mellifera using whole genome bisulfite sequencing (WGBS) method.

285 m DNA methylation, we performed whole genome bisulfite sequencing (WGBS) on an equimolar pool of sper

286 The cost of whole-genome bisulfite sequencing (WGBS) remains a bottleneck for man

287 Whole genome bisulfite sequencing (WGBS) revealed that integrin alpha

288 Recent developments in whole genome bisulfite sequencing (WGBS) technology have enabled geno

289 increased disease risk we used whole genome bisulfite sequencing (WGBS) to analyze changes in DNA me

290 Here, whole genome bisulfite sequencing (WGBS) was used to assess the effec

291 Pipelines are provided for whole genome bisulfite sequencing (WGBS), reduced representation bisu

292 Whole genome bisulfite sequencing (WGBS), with its ability to interro

293 methylated regions (DMRs) from whole-genome bisulfite sequencing (WGBS).

294 single base pair resolution by whole genome bisulfite sequencing (WGBS).

295 e increases in methylation were validated by bisulfite sequencing, where they occurred in a minority

296 Here, we performed whole-genome bisulfite sequencing, which is a comprehensive and unbia

297 dresses statistical challenges introduced by bisulfite-sequencing while controlling for complex sourc

298 e used whole-genome sequencing, whole-genome bisulfite sequencing, whole transcriptome (RNA-seq) and

299 ned using single cell reduced representation bisulfite sequencing, with a 66-fold increase in the fra

300 rporation of the 5D4 DNA polymerase into the bisulfite sequencing workflow thus promises significant