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1 FAIRE (formaldehyde-assisted isolation of regulatory ele
2 FAIRE has low technical variability, which allows its us
3 FAIRE has utility as a positive selection for genomic re
4 FAIRE induction was universally decreased by Brg-1 deple
5 FAIRE performed in human cells strongly enriches DNA coi
7 erse human cell types, we used DNase-seq and FAIRE-seq (Formaldehyde Assisted Isolation of Regulatory
8 bulk samples such as ChIP-seq, DNase-seq and FAIRE-seq cannot analyze samples with small numbers of c
11 latory elements to extract protein-free DNA (FAIRE) and the MNase-mediated purification of mononucleo
13 e-Assisted Isolation of Regulatory Elements (FAIRE) procedure and use it to determine the rate of cro
14 e-assisted isolation of regulatory elements (FAIRE) quantitative PCR and chromatin immunoprecipitatio
15 e-assisted isolation of regulatory elements (FAIRE) revealed chromatin conformation changes that were
16 e-assisted isolation of regulatory elements (FAIRE) to map open chromatin during the transition from
17 e-assisted isolation of regulatory elements (FAIRE), a chemical method to enrich for nucleosome-deple
18 e-assisted isolation of regulatory elements (FAIRE), does not affect the accessible chromatin signal.
21 ong midline FAIRE peak and weak whole-embryo FAIRE peak overlap with known midline enhancers and prov
26 n of this method of enhanced cavitation into FAIRE offers the potential for extending chromatin acces
27 rs7903146 showed allelic imbalance in islet FAIRE signals and that the variant alters enhancer activ
28 Midline enhancer fragments with a midline FAIRE peak tend to be near midline-expressed genes, wher
29 whereas midline enhancers without a midline FAIRE peak were often distant from midline-expressed gen
30 regions of the genome with a strong midline FAIRE peak and weak whole-embryo FAIRE peak overlap with
31 midline cells was performed and the midline FAIRE data were compared with whole-embryo FAIRE data.
34 map "open chromatin." Over 870,000 DNaseI or FAIRE sites, which correspond tightly to nucleosome-depl
40 hort-read sequencing technologies (ChIP-seq, FAIRE-seq, MNase-Seq, ...) and offers innovative approac
43 data from a variety of ChIP-seq, DNase-seq, FAIRE-seq, and ATAC-seq experiments, we show that our we
44 s) combined with next-generation sequencing (FAIRE-seq) to identify specific changes in chromatin acc
45 ents followed by next-generation sequencing (FAIRE-seq) to map regions of open chromatin in three pri
47 ority GR-responsive regions shared a similar FAIRE signal in the basal chromatin state, suggesting a
49 Using 548 ENCODE ChIP-seq and six targeted FAIRE-seq samples, we show that BaalChIP effectively cor
50 me-depleted DNA from human chromatin, termed FAIRE (Formaldehyde-Assisted Isolation of Regulatory Ele
51 ion of cis-regulatory elements and show that FAIRE-seq can guide the identification of regulatory var