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

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

2 Chromatin immunoprecipitation sequencing analyses identi

3 In addition, chromatin immunoprecipitation sequencing analyses showed

4 Gene profiling and chromatin immunoprecipitation sequencing analyses unrave

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

6 We performed Sp7 chromatin immunoprecipitation sequencing analysis identi

7 Chromatin immunoprecipitation sequencing analysis of the

8 Chromatin immunoprecipitation sequencing analysis reveal

9 Chromatin immunoprecipitation sequencing analysis sugges

10 Chromatin immunoprecipitation sequencing analysis with i

11 Chromatin immunoprecipitation-sequencing analysis of Isl

12 Genome-wide chromatin immunoprecipitation-sequencing analysis reveal

13 Chromatin immunoprecipitation sequencing and gene expres

14 Chromatin immunoprecipitation sequencing and gene expres

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

16 Using chromatin immunoprecipitation sequencing and luciferase

17 Chromatin immunoprecipitation sequencing and methylation

18 Using a combination of chromatin immunoprecipitation sequencing and microarray

19 Our distribution was supported by chromatin immunoprecipitation sequencing and microarray

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

21 Quantitative chromatin immunoprecipitation sequencing and promoter re

22 Utilizing chromatin immunoprecipitation sequencing and RNA sequenc

23 We used chromatin immunoprecipitation sequencing and RNA sequenc

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

25 Dynamic chromatin immunoprecipitation sequencing and self-transc

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

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

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

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

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

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

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

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

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

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

36 Chromatin immunoprecipitation sequencing (ChIP-seq) and

37 Using chromatin immunoprecipitation sequencing (ChIP-seq) comb

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

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

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

41 Chromatin immunoprecipitation sequencing (ChIP-seq) expe

42 Chromatin immunoprecipitation sequencing (ChIP-seq) expe

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

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

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

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

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

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

49 Chromatin immunoprecipitation sequencing (ChIP-seq) reve

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

51 Chromatin immunoprecipitation sequencing (ChIP-Seq) show

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

86 In chromatin immunoprecipitation sequencing, cyclin D1 occu

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

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

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

90 Analysis of chromatin immunoprecipitation sequencing data sets for M

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

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

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

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

95 Genome-wide chromatin immunoprecipitation sequencing experiments rev

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

97 Chromatin immunoprecipitation-sequencing experiments fol

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

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

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

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

102 Chromatin immunoprecipitation sequencing illustrates tha

103 Chromatin immunoprecipitation sequencing in chick limb b

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

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

106 Chromatin immunoprecipitation sequencing in T helper 17

107 Chromatin immunoprecipitation-sequencing in lymphoblasto

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

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

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

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

112 Chromatin immunoprecipitation-sequencing results for sev

113 Chromatin immunoprecipitation sequencing revealed H3K27m

114 Chromatin immunoprecipitation sequencing revealed that i

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

116 Furthermore, chromatin immunoprecipitation sequencing revealed that t

117 Chromatin immunoprecipitation sequencing revealed the tr

118 Chromatin immunoprecipitation sequencing reveals 4785 p5

119 Moreover, chromatin immunoprecipitation-sequencing reveals BRG1 bi

120 Chromatin immunoprecipitation-sequencing reveals that TF

121 Furthermore, microarray and chromatin immunoprecipitation sequencing screens led to

122 Chromatin immunoprecipitation sequencing showed that a l

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

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

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

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

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

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

129 We used chromatin immunoprecipitation-sequencing to identify 406

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

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

132 Using chromatin immunoprecipitation sequencing, we demonstrate

133 Using chromatin immunoprecipitation sequencing, we identified

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