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1 ChIA-PET is a high-throughput mapping technology that re
2 ChIA-PET is rapidly emerging as an important experimenta
4 n (ChIP) and chromatin interaction analysis (ChIA-PET), we determined genome-wide SOX2-bound regions
5 P-seq, GRO-seq, STARR-seq, RNA-seq, Hi-C and ChIA-PET data in five human cancer cell lines, we identi
6 reported by Hi-C, promoter capture Hi-C and ChIA-PET experiments and in capturing previously validat
7 n from publicly available datasets (Hi-C and ChIA-PET), and correlated activity links that we infer a
8 on capture (3C) technology, such as Hi-C and ChIA-PET, have demonstrated the importance of 3D genome
9 capture (3C) technologies, such as Hi-C and ChIA-PET, have the potential to elucidate the functional
10 enced individuals with LCL-specific Hi-C and ChIA-PET-based chromatin contact maps to uncover one of
11 n proximity-ligation assays, like HiChIP and ChIA-PET, facilitate the accurate identification of long
12 matin binding data in mammary cell lines and ChIA-PET chromatin interaction data from ENCODE, we iden
13 tested on 12 ChIP-seq, ATAC-seq, RNA-seq and ChIA-PET datasets, pyBedGraph is on average 260 times fa
14 sequencing experiments such as ChIP-seq and ChIA-PET that generate coverage files for transcription
15 bined DNaseI hypersensitivity, ChIP-seq, and ChIA-PET technologies to map the promoter-enhancer inter
17 atin interaction data from protocols such as ChIA-PET, HiChIP and Hi-C provide valuable insights into
18 vailability of orthogonal data types such as ChIA-PET, HiChIP, Capture Hi-C, and high-throughput imag
19 oter capture Hi-C and Hi-Cap data as well as ChIA-PET data from mouse embryonic stem cells to investi
21 Application of Mango to multiple available ChIA-PET datasets permitted the independent rediscovery
22 by learning the latent relationships between ChIA-PET and two widely used data types: Hi-C and ChIP-s
23 models with contact frequencies observed by ChIA-PET and Hi-C genomic-driven methods to examine the
30 hIA-ET in GM12878 and HeLa but also non-CTCF ChIA-PET interactions, including RNA polymerase II (RNAP
32 ors, whole-genome bisulfite sequencing data, ChIA-PET data, and functional data in several biosamples
33 ds of ChIA-PET data generated from different ChIA-PET protocols and also provides quality controls fo
36 lidation of these predictions using existing ChIA-PET and Hi-C data sets showed that RIPPLE accuratel
37 ChIA-PET2 integrates all steps required for ChIA-PET data analysis, including linker trimming, read
38 present Model based Interaction Calling from ChIA-PET data (MICC), an easy-to-use R package to detect
42 ping interactions between DNA regions, e.g., ChIA-PET and HiC, can generate genome-wide maps of inter
44 romatin structure data and RNA polymerase II ChIA-PET data from MCF-7 cells did not suggest remote ef
47 s, including a hypergeometric model (used in ChIA-PET tool), MICC (used in ChIA-PET2), ChiaSig and ma
49 interactions through deeper and integrative ChIA-PET data analysis and demonstrates DNA looping pred
54 e trained our deep models with CTCF-mediated ChIA-PET of GM12878 as ground truth, and the deep networ
60 le pipeline for analyzing different types of ChIA-PET data from raw sequencing reads to chromatin loo
63 tions, which were undetected in the original ChIA-PET paper but were validated by other independent e
65 omparison to the existing software packages, ChIA-PET Tool and ChiaSig revealed that Mango interactio
67 earning approach that can accurately predict ChIA-PET interactions by learning the latent relationshi
68 stent with Cohesin extrusion and can predict ChIA-PET CTCF looping interaction measurements with high
69 mputational method for accurately predicting ChIA-PET interactions from Hi-C and ChIP-seq data is nee
72 o executes all steps required for processing ChIA-PET datasets, whereas ChiaSig only completes 20% of
73 STACHE recovers a higher number of published ChIA-PET and HiChIP loops as well as loops linking promo
74 user may generate structures using published ChIA-PET data for the GM12878 cell line by simply specif
77 provide the detailed protocol for long-read ChIA-PET that includes cell fixation and lysis, chromati
78 he original approach by developing long-read ChIA-PET, in which the length of the paired-end tags is
79 ctions, including RNA polymerase II (RNAPII) ChIA-PET of GM12878, RAD21 ChIA-PET of GM12878, and RAD2
80 ction analysis by paired-end tag sequencing (ChIA-PET) can capture genome-wide chromatin interactions
81 lysis followed by paired-end tag sequencing (ChIA-PET) data linked EBV enhancers to 90% of EBV-regula
82 alysis by in-situ Paired-End Tag Sequencing (ChIA-PET) data, we confirmed that SCI sub-compartment pr
83 ction Analysis by Paired-End Tag sequencing (ChIA-PET) experiments targeting six broadly distributed
84 ction analysis by paired-end tag sequencing (ChIA-PET) is a method for the genome-wide de novo discov
85 ction Analysis by Paired-End Tag Sequencing (ChIA-PET) is a popular assay method for studying genome-
86 ction analysis by paired-end tag sequencing (ChIA-PET) is a robust method for capturing genome-wide c
87 ction Analysis by Paired-End Tag sequencing (ChIA-PET) is an established method for detecting genome-
88 ion analysis with paired-end tag sequencing (ChIA-PET) of the cohesin subunit SMC1A in developing mou
89 ction analysis by paired-end tag sequencing (ChIA-PET) strategy to comprehensively map higher-order c
90 ction analysis by paired-end tag sequencing (ChIA-PET) to comprehensively identify genome-wide associ
91 ction analysis by paired-end tag sequencing (ChIA-PET), and analysed gene expression in 24 diverse hu
93 lysis followed by paired-end tag sequencing (ChIA-PET), and genome-wide clustered regularly interspac
95 ction analysis by paired-end tag sequencing, ChIA-PET)(3), have revealed topologically associating do
97 atin interaction analysis by paired-end tag (ChIA-PET) reveals that rhythmic BMAL1 target gene expres
98 atin interaction analysis by paired-end tag (ChIA-PET) sequencing data, we used CRISPR-Cas9 gene edit
99 atin Interaction Analysis by Paired-End Tag (ChIA-PET), in situ Hi-C followed by chromatin immunoprec
103 A-PET is an accurate tool for predicting the ChIA-PET interactions mediated by various chromatin-asso
106 rence 3D genome structure is generated using ChIA-PET data from the GM12878 cell line and SVs data ar
107 ancer-promoter interactions identified using ChIA-PET in mouse ESCs, and confirm previously validated
109 first high-resolution 3D genome mapping via ChIA-PET to capture RNAPII-associated chromatin interact