The Genomic HyperBrowser: inferential genomics at the sequence level
about
Hot spots of DNA double-strand breaks and genomic contacts of human rDNA units are involved in epigenetic regulationGenomic regions associated with multiple sclerosis are active in B cellsHandling realistic assumptions in hypothesis testing of 3D co-localization of genomic elements.The PinkThing for analysing ChIP profiling data in their genomic contextThe Genomic HyperBrowser: an analysis web server for genome-scale data.Confero: an integrated contrast data and gene set platform for computational analysis and biological interpretation of omics data.Identifying pathogenic processes by integrating microarray data with prior knowledgeClusTrack: feature extraction and similarity measures for clustering of genome-wide data setsVisRseq: R-based visual framework for analysis of sequencing data.Chromatin states reveal functional associations for globally defined transcription start sites in four human cell lines.The ETS family member GABPα modulates androgen receptor signalling and mediates an aggressive phenotype in prostate cancerHuman-specific epigenetic variation in the immunological Leukotriene B4 Receptor (LTB4R/BLT1) implicated in common inflammatory diseasesThe differential disease regulomeIdentifying elemental genomic track types and representing them uniformly.Age-associated hyper-methylated regions in the human brain overlap with bivalent chromatin domainsIdentification, characterization and distribution of transposable elements in the flax (Linum usitatissimum L.) genome.Integrating multiple oestrogen receptor alpha ChIP studies: overlap with disease susceptibility regions, DNase I hypersensitivity peaks and gene expression.The dilemma of choosing the ideal permutation strategy while estimating statistical significance of genome-wide enrichmentPrediction of Gene Activity in Early B Cell Development Based on an Integrative Multi-Omics AnalysisVitamin D receptor ChIP-seq in primary CD4+ cells: relationship to serum 25-hydroxyvitamin D levels and autoimmune diseaseSequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversityTranscriptional reprogramming of CD11b+Esam(hi) dendritic cell identity and function by loss of Runx3.HiBrowse: multi-purpose statistical analysis of genome-wide chromatin 3D organization.Transcriptionally active regions are the preferred targets for chromosomal HPV integration in cervical carcinogenesis.EBNA2 binds to genomic intervals associated with multiple sclerosis and overlaps with vitamin D receptor occupancy.Hidden among the crowd: differential DNA methylation-expression correlations in cancer occur at important oncogenic pathwaysAutomated amplicon design suitable for analysis of DNA variants by melting techniques.An integrative analysis of post-translational histone modifications in the marine diatom Phaeodactylum tricornutum.Generation of a synthetic GlcNAcylated nucleosome reveals regulation of stability by H2A-Thr101 GlcNAcylation.Vitamin D receptor binding, chromatin states and association with multiple sclerosis.Coordinates and intervals in graph-based reference genomesBioinformatics Analysis of Estrogen-Responsive Genes.Male-Specific Transcription Factor Occupancy Alone Does Not Account for Differential Methylation at Imprinted Genes in the mouse Germ Cell Lineage.Effects of sulforaphane and 3,3'-diindolylmethane on genome-wide promoter methylation in normal prostate epithelial cells and prostate cancer cells.Estimated comparative integration hotspots identify different behaviors of retroviral gene transfer vectors.GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenomeFunctional redundancy in the nuclear compartmentalization of the late-replicating genomeHuman somatic cell mutagenesis creates genetically tractable sarcomas.Integrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcomaSequential Monte Carlo multiple testing.
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P2860
The Genomic HyperBrowser: inferential genomics at the sequence level
description
2010 nî lūn-bûn
@nan
2010 թուականին հրատարակուած գիտական յօդուած
@hyw
2010 թվականին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
The Genomic HyperBrowser: inferential genomics at the sequence level
@ast
The Genomic HyperBrowser: inferential genomics at the sequence level
@en
The Genomic HyperBrowser: inferential genomics at the sequence level
@en-gb
The Genomic HyperBrowser: inferential genomics at the sequence level
@nl
type
label
The Genomic HyperBrowser: inferential genomics at the sequence level
@ast
The Genomic HyperBrowser: inferential genomics at the sequence level
@en
The Genomic HyperBrowser: inferential genomics at the sequence level
@en-gb
The Genomic HyperBrowser: inferential genomics at the sequence level
@nl
prefLabel
The Genomic HyperBrowser: inferential genomics at the sequence level
@ast
The Genomic HyperBrowser: inferential genomics at the sequence level
@en
The Genomic HyperBrowser: inferential genomics at the sequence level
@en-gb
The Genomic HyperBrowser: inferential genomics at the sequence level
@nl
P2093
P2860
P50
P3181
P1433
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The Genomic HyperBrowser: inferential genomics at the sequence level
@en
P2093
Egil Ferkingstad
Halfdan Rydbeck
Marit Holden
Morten Johansen
Sveinung Gundersen
Vegard Nygaard
P2860
P2888
P3181
P356
10.1186/GB-2010-11-12-R121
P407
P50
P577
2010-01-01T00:00:00Z
P5875
P6179
1008128012