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Links from GEO DataSets

Items: 20

1.

Ludwig Institute/UCSD ENCODE project March 2007 Release

(Submitter supplied) The readout of genome information is controlled by transcriptional regulatory elements, but a comprehensive view of the combinatorial control by these DNA sequences, which bind regulatory protein and/or the modified histones in regulating gene transcription, is clearly preliminary. We have developed an experimental strategy for comprehensive determination of such functional elements in human DNA. This strategy involves the application of genome-wide location analysis, also known as ChIP-chip, to a panel of well-characterized regulatory proteins and histones with specific modifications, known to generally associate with transcriptional regulatory elements in vivo. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL1454 GPL4559
124 Samples
Download data: GPR, PAIR
2.

Global Chromatin Modifications at Enhancers Correlate with Cell Type-Specific Gene Expression in the Human Genome

(Submitter supplied) The human body is composed of diverse cell types with distinct functions. While it is known that lineage specification depends on cell specific gene expression, which in turn is driven by promoters, enhancers, insulators and other cis-regulatory DNA sequences for each gene1-3, the relative roles of these regulatory elements in this process is not clear. We have previously developed a chromatin immunoprecipitation-based microarray method (ChIP-chip) to identify promoters, enhancers and insulator elements in the human genome4-6. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array; Expression profiling by array
97 related Platforms
235 Samples
Download data: CEL
Series
Accession:
GSE14083
ID:
200014083
3.

Differential roles of promoters, enhancers, and insulators in cell-type specific gene expression

(Submitter supplied) Chromatin immunoprecipitation was performed using antibodies against CTCF and formaldehyde crosslinked chromatin from K562 Chromatin cells. The immunoprecipitated DNA was amplified, fluorescently labeled and hybridized to a 391K element tiling array based on NCBI35 build of the human genome (hg17) that contains overlapping 50-mer oligonucleotides, positioned at every 38 basepairs (bp) throughout the ENCODE regions. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL4559
3 Samples
Download data: PAIR
Series
Accession:
GSE8098
ID:
200008098
4.

Ludwig Institute/UCSD ENCODE project June 2007 Release

(Submitter supplied) The readout of genome information is controlled by transcriptional regulatory elements, but a comprehensive view of the combinatorial control by these DNA sequences, which bind regulatory protein and/or the modified histones in regulating gene transcription, is clearly preliminary. We have developed an experimental strategy for comprehensive determination of such functional elements in human DNA. This strategy involves the application of genome-wide location analysis, also known as ChIP-chip, to a panel of well-characterized regulatory proteins and histones with specific modifications, known to generally associate with transcriptional regulatory elements in vivo. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL4559 GPL1454
51 Samples
Download data: GPR, PAIR
5.

Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome

(Submitter supplied) Eukaryotic gene regulatory information is contained within the DNA sequences of cis-regulatory elements and the epigenetic features of the chromatin surrounding these elements. Recent investigations in yeast, fly, and mammalian systems have made significant contributions toward our understanding of the relationship between gene activation and chromatin architecture at transcriptional promoters, but much work remains to improve our knowledge of this relationship at human promoters and other transcriptional regulatory elements, such as enhancers. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL4558 GPL4559 GPL1454
64 Samples
Download data
6.

CD34 blood cells

(Submitter supplied) CD34+ positively isolated from healthy donors (stimulated by G-CSF) with magnetic beads (after blood leukapheresis) CD34- obtained from 10dd cytokine cultured CD34+ Keywords: differentiation
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
5 Samples
Download data: CEL
Series
Accession:
GSE11092
ID:
200011092
7.

The Genome Wide Distribution of Acetylated Histone H4 Remodelled through Human Primary Myoblast Differentiation

(Submitter supplied) The simultaneous genotyping of tens of thousands of SNP using SNP microarrays is a very important tool that is revolutionizing genetics and molecular biology. In this work, we present a new application of this technique by using it to assess chromatin immunoprecipitation (CHIP) as a means to assess the multiple genomic locations bound by a protein complex recognized by an antibody. We illustrate the use of this technique with an analysis of the change in histone H4 acetylation, a marker of open chromatin and transcriptionally active genomic regions, which occur during the differentiation of human myoblasts into myotubes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL97 GPL3400 GPL96
21 Samples
Download data: CEL, EXP
Series
Accession:
GSE4133
ID:
200004133
8.

Mapping of H4-acetylated chromatin modifications in differentiating human primary myoblasts

(Submitter supplied) We assessed the genomic distribution of H4-acetylated chromatin by ChIP using SNP chips and an antibody specific to four acetylated lysine residues of H4. Keywords: Comparative genomic hybridization
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by SNP array; SNP genotyping by SNP array
Platform:
GPL3400
9 Samples
Download data: CEL, EXP
Series
Accession:
GSE4132
ID:
200004132
9.

Determination of myotube and myoblast expression levels

(Submitter supplied) Gene expression was determined for both myotubes and myoblasts using Affymetrix HG-U133 A/B arrays. Keywords: Comparative expression
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL97 GPL96
12 Samples
Download data: CEL, EXP
Series
Accession:
GSE4131
ID:
200004131
10.

DNaseI sensitivity/hypersensitivity Part I

(Submitter supplied) DNaseI sensitivity/hypersensitivity using DNase-array method (Sabo et al Nature Methods 3:511-18, 2006) on Affymetrix whole-genome tiling DNA microarrays. Background: Focal alteration in chromatin structure in vivo, detectable through hypersensitivity to DNaseI and other nucleases, is the sine qua non of diverse transcriptional regulatory elements including enhancers, promoters, insulators, and locus control regions. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
7 related Platforms
76 Samples
Download data: CEL
Series
Accession:
GSE7168
ID:
200007168
11.

DNaseI/Array multiple cell types

(Submitter supplied) The goal of this study was to map DNaseI sensitivity and DNaseI hypersensitive sites over the ENCODE regions in multiple human cell types (GM06990, CACO2, HepG2). Keywords: DNase/Array
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL2131
3 Samples
Download data: PDF, TXT
Series
Accession:
GSE8177
ID:
200008177
12.

DNaseI/Array GM06990

(Submitter supplied) The goal of this study was to map DNaseI sensitivity and DNaseI hypersensitive sites over the ENCODE regions in human lymphoblastoid cells (GM06990, Coriell). Keywords: DNase/Array
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL2131
1 Sample
Download data
13.

Genome wide mapping of transcription factor downstream targets using STAGE

(Submitter supplied) Identifying the chromosomal targets of transcription factors is important for reconstructing the transcriptional regulatory networks underlying global gene expression programs. We have developed an unbiased genomic method called sequence tag analysis of genomic enrichment (STAGE) to identify the direct binding targets of transcription factors in vivo. STAGE is based on high-throughput sequencing of concatemerized tags derived from target DNA enriched by chromatin immunoprecipitation. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL1485
2 Samples
Download data
Series
Accession:
GSE6312
ID:
200006312
14.

2091 mock vs. 2091 E2F4 IP - Human 13K

(Submitter supplied) 2091 mock vs. 2091 E2F4 IP - Human 13K promoter microarray 2091 cells were serum starved for 72hours and fixed with formaldehyde. Keywords: repeat sample
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1525
2 Samples
Download data
Series
Accession:
GSE1861
ID:
200001861
15.

Chromatin proteomics reveals novel combinatorial histone modification signatures that mark distinct subpopulations of macrophage enhancers

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
30 Samples
Download data: BROADPEAK, BW, NARROWPEAK, TXT
Series
Accession:
GSE91009
ID:
200091009
16.

Chromatin proteomics reveals novel combinatorial histone modification signatures that mark distinct subpopulations of macrophage enhancers [RNA-seq]

(Submitter supplied) The activity of enhancers and promoters fine-tunes the transcriptional program of mammalian cells through the recruitment and interplay between cell type-specific and ubiquitous transcription factors. Despite their key role in modulating transcription, the identification of enhancers is challenged by their limited sequence conservation and highly variable distance from target genes. Although enhancers are characterised by the strong enrichment of mono-methylation at lysine 4 of histone H3, mirrored by low tri-methylation at the same residue, a comprehensive list of enhancers-associated histone post-translational modifications (PTMs) is still lacking. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
1 Sample
Download data: TXT
Series
Accession:
GSE91008
ID:
200091008
17.

Chromatin proteomics reveals novel combinatorial histone modification signatures that mark distinct subpopulations of macrophage enhancers [ChIP-seq]

(Submitter supplied) The activity of enhancers and promoters fine-tunes the transcriptional program of mammalian cells through the recruitment and interplay between cell type-specific and ubiquitous transcription factors. Despite their key role in modulating transcription, the identification of enhancers is challenged by their limited sequence conservation and highly variable distance from target genes. Although enhancers are characterised by the strong enrichment of mono-methylation at lysine 4 of histone H3, mirrored by low tri-methylation at the same residue, a comprehensive list of enhancers-associated histone post-translational modifications (PTMs) is still lacking. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
29 Samples
Download data: BED, BROADPEAK, BW, NARROWPEAK
Series
Accession:
GSE91007
ID:
200091007
18.

In vivo epigenomic profiling of germ cells reveals germ cell molecular signatures

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL6887 GPL9250 GPL9185
42 Samples
Download data: WIG
Series
Accession:
GSE38165
ID:
200038165
19.

In vivo epigenomic profiling of germ cells reveals germ cell molecular signatures [ChIP-Seq]

(Submitter supplied) The limited number of in vivo germ cells poses an impediment to genome-wide studies. Here, we applied a small-scale ChIP-Seq method on purified mouse fetal germ cells to generate genome-wide maps of four histone modifications (H3K4me3, H3K27me3, H3K27ac and H2BK20ac), facilitating the identification of active and repressed cis-regulatory elements in germ cells in vivo. Comparison of active chromatin state between somatic, embryonic stem cells (ESC) and germ cells revealed promoters and enhancers needed for stem cell maintenance and germ cell development. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9250 GPL9185
31 Samples
Download data: WIG
Series
Accession:
GSE38164
ID:
200038164
20.

Expression profiling of FACS-purified fetal germ cells

(Submitter supplied) We used microarrays to profile global gene expression changes of Pou5f1-GFP-positive germ cells between E11.5 to E15.5.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
11 Samples
Download data: TXT
Series
Accession:
GSE38126
ID:
200038126
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