Extensive variation in chromatin states across humans. - Wikidata - wikimedia - TriplyDB

Extensive variation in chromatin states across humans.

Extensive variation in chromatin states across humans.

http://www.wikidata.org/entity/Q33823781

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Synthetic CpG islands reveal DNA sequence determinants of chromatin structure Regulatory Variants and Disease: The E-Cadherin -160C/A SNP as an Example Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association Exploiting genomics and natural genetic variation to decode macrophage enhancers Variation in vertebrate cis-regulatory elements in evolution and disease Enhancer malfunction in cancer Transcriptional Dynamics at Brain Enhancers: from Functional Specialization to Neurodegeneration The selection and function of cell type-specific enhancers Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions The genetic and mechanistic basis for variation in gene regulation Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression Evidence for a common evolutionary rate in metazoan transcriptional networks Epigenome data release: a participant-centered approach to privacy protection Genetic and epigenetic variation in the lineage specification of regulatory T cells.Methods of integrating data to uncover genotype-phenotype interactions.Recommendations for Accurate Resolution of Gene and Isoform Allele-Specific Expression in RNA-Seq Data.Removing reference mapping biases using limited or no genotype data identifies allelic differences in protein binding at disease-associated loci.SNPhood: investigate, quantify and visualise the epigenomic neighbourhood of SNPs using NGS data Predictive long-range allele-specific mapping of regulatory variants and target transcripts.Laying a solid foundation for Manhattan--'setting the functional basis for the post-GWAS era'.Natural variation of histone modification and its impact on gene expression in the rat genome.A promoter-proximal transcript targeted by genetic polymorphism controls E-cadherin silencing in human cancers.Taming Human Genetic Variability: Transcriptomic Meta-Analysis Guides the Experimental Design and Interpretation of iPSC-Based Disease Modeling.Genetic factors underlying discordance in chromatin accessibility between monozygotic twins.The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes.Prediction of Chromatin Accessibility in Gene-Regulatory Regions from Transcriptomics Data.NGSCheckMate: software for validating sample identity in next-generation sequencing studies within and across data types.Sequence-level mechanisms of human epigenome evolution.Nucleosome repositioning links DNA (de)methylation and differential CTCF binding during stem cell development.Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis.Genetic-epigenetic dysregulation of thymic TSH receptor gene expression triggers thyroid autoimmunity Transcription factor binding predicts histone modifications in human cell lines Predicting the human epigenome from DNA motifs.PRDM9 drives evolutionary erosion of hotspots in Mus musculus through haplotype-specific initiation of meiotic recombination.Epigenetic remodelling and dysregulation of DLGAP4 is linked with early-onset cerebellar ataxia The pancreatic β cell: recent insights from human genetics.Explicit DNase sequence bias modeling enables high-resolution transcription factor footprint detection.Fine mapping and candidate gene search of quantitative trait loci for growth and obesity using mouse intersubspecific subcongenic intercrosses and exome sequencing.Approaches for establishing the function of regulatory genetic variants involved in disease.

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Extensive variation in chromatin states across humans.

http://www.wikidata.org/entity/Q33823781

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2013 nî lūn-bûn

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2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2013年の論文

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Extensive variation in chromatin states across humans.

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Extensive variation in chromatin states across humans.

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Extensive variation in chromatin states across humans.

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Extensive variation in chromatin states across humans.

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Extensive variation in chromatin states across humans.

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Extensive variation in chromatin states across humans.

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Extensive variation in chromatin states across humans.

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Anthony Olarerin-George

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Damek V Spacek

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Dan Xie

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Fabian Grubert

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Fouad Zakharia

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Jingjing Li

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John B Hogenesch

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Maya Kasowski

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Michael Snyder

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Qiangfeng Cliff Zhang

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P2860

Model-based analysis of ChIP-Seq (MACS)

Differential expression analysis for sequence count data

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

An integrated encyclopedia of DNA elements in the human genome

An integrated map of genetic variation from 1,092 human genomes

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Mathematical model for studying genetic variation in terms of restriction endonucleases

GENCODE: the reference human genome annotation for The ENCODE Project

A map of human genome variation from population-scale sequencing

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750-752

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10.1126/SCIENCE.1242510

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6159

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342

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Lars M Steinmetz

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2013-10-17T00:00:00Z

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