Multiplexed analysis of chromosome conformation at vastly improved sensitivity
about
The second decade of 3C technologies: detailed insights into nuclear organizationClosing the loop: 3C versus DNA FISHA hyperactive transcriptional state marks genome reactivation at the mitosis-G1 transition.HiChIP: efficient and sensitive analysis of protein-directed genome architecture.Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity.Genetic dissection of the α-globin super-enhancer in vivo.Genetic and epigenetic factors underlying sex differences in the regulation of gene expression in the brain.MLL-AF4 binds directly to a BCL-2 specific enhancer and modulates H3K27 acetylationMultiple renal cancer susceptibility polymorphisms modulate the HIF pathway.Capture-C reveals preformed chromatin interactions between HIF-binding sites and distant promotersUnlinking an lncRNA from Its Associated cis Element.Mining the Unknown: Assigning Function to Noncoding Single Nucleotide Polymorphisms.Capturing genomic relationships that matterChallenges and progress in interpretation of non-coding genetic variants associated with human disease.Genetic variation at the 8q24.21 renal cancer susceptibility locus affects HIF binding to a MYC enhancer.Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemiaFunctional characterisation of cis-regulatory elements governing dynamic Eomes expression in the early mouse embryoThree-dimensional genome architecture and emerging technologies: looping in disease.Robust detection of chromosomal interactions from small numbers of cells using low-input Capture-C.Low-input Capture-C: A Chromosome Conformation Capture Assay to Analyze Chromatin Architecture in Small Numbers of Cells.A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene Expression.Comparative analysis of three-dimensional chromosomal architecture identifies a novel fetal hemoglobin regulatory element.Sasquatch: predicting the impact of regulatory SNPs on transcription factor binding from cell- and tissue-specific DNase footprints.Integration of human pancreatic islet genomic data refines regulatory mechanisms at Type 2 Diabetes susceptibility loci.Tissue-specific CTCF-cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo.Between form and function: the complexity of genome folding.Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.4Cin: A computational pipeline for 3D genome modeling and virtual Hi-C analyses from 4C data.3C and 3C-based techniques: the powerful tools for spatial genome organization deciphering.A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsCommentary: Nuclear dynamics of the Set1C subunit Spp1 prepares meiotic recombination sites for break formationStage-specific epigenetic regulation of CD4 expression by coordinated enhancer elements during T cell development
P2860
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P2860
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
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2015年學術文章
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name
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
@ast
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
@en
type
label
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
@ast
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
@en
prefLabel
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
@ast
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
@en
P2093
P2860
P50
P356
P1433
P1476
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
@en
P2093
James O J Davies
Jim R Hughes
Stephen Taylor
P2860
P2888
P356
10.1038/NMETH.3664
P577
2015-11-23T00:00:00Z
P6179
1006820435