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Links from GEO DataSets

Items: 20

1.

Genome-wide mapping of nucleosome positioning and DNA methylation within Individual DNA molecules

(Submitter supplied) DNA methylation and nucleosome positioning work together to generate chromatin structures that regulate gene expression. Nucleosomes are typically mapped using nuclease digestion requiring significant amounts of material and varying enzyme concentrations. We have developed a method (NOMe-seq) that uses a GpC methyltransferase (M.CviPI) and next generation sequencing to generate a high resolution footprint of nucleosome positioning genome-wide using less than 1 million cells while retaining endogenous DNA methylation information from the same DNA strand. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL11154
3 Samples
Download data: WIG
Series
Accession:
GSE40770
ID:
200040770
2.

Nucleosome map of the IMR90 fibroblast cell line

(Submitter supplied) We produced a map of nucleosome positions in IMR90 by sequencing the ends of MNase-digested chromatin fragments.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
1 Sample
Download data: BAM
Series
Accession:
GSE21823
ID:
200021823
3.

Nucleosome deposition and DNA methylation at coding region boundaries

(Submitter supplied) We profiled CpG methylation for human T cells and compared this pattern with public T cell nucleosome (H2A.Z) and polymerase II profiles (SRA000234). Focusing on DNA regions surrounding the start codon and stop codon, instead of the transcription start and end sites, we discovered a very intriguing pattern, namely methylation and nucleosomal peaks at those regions, more prominent than peaks near transcript boundaries. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL9052
1 Sample
Download data: BED
Series
Accession:
GSE17554
ID:
200017554
4.

NOMe-seq of mouse embryonic stem cells

(Submitter supplied) We report NOMe-seq data obtained from mouse embryonic stem cells
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL19057
1 Sample
Download data: WIG
Series
Accession:
GSE122964
ID:
200122964
5.

Relationship between nucleosome positioning and DNA methylation: Bisulfite-Seq, ChIP-Seq, and Mnase-Seq

(Submitter supplied) Nucleosomes compact and regulate access to DNA in the nucleus, and are composed of approximately 147 bases of DNA wrapped around a histone octamer. Here we report a genome-wide nucleosome positioning analysis of Arabidopsis thaliana utilizing massively parallel sequencing of mononucleosomes. By combining this data with profiles of DNA methylation at single base resolution, we identified ten base periodicities in the DNA methylation status of nucleosome-bound DNA and found that nucleosomal DNA was more highly methylated than flanking DNA. more...
Organism:
Arabidopsis thaliana; Homo sapiens
Type:
Methylation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9062 GPL9115 GPL9302
4 Samples
Download data: TXT
Series
Accession:
GSE21821
ID:
200021821
6.

Relationship between nucleosome positioning and DNA methylation: ChIP-chip

(Submitter supplied) Nucleosomes compact and regulate access to DNA in the nucleus, and are composed of approximately 147 bases of DNA wrapped around a histone octamer1, 2. Here we report a genome-wide nucleosome positioning analysis of Arabidopsis thaliana utilizing massively parallel sequencing of mononucleosomes. By combining this data with profiles of DNA methylation at single base resolution, we identified ten base periodicities in the DNA methylation status of nucleosome-bound DNA and found that nucleosomal DNA was more highly methylated than flanking DNA. more...
Organism:
Arabidopsis thaliana
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL10977 GPL10978
2 Samples
Download data: BAR, CEL
Series
Accession:
GSE21818
ID:
200021818
7.

Relationship between nucleosome positioning and DNA methylation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Arabidopsis thaliana
Type:
Methylation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Genome binding/occupancy profiling by genome tiling array
5 related Platforms
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE21673
ID:
200021673
8.

Genome-wide maps of nucleosome occupancy in human lymphoblastoid cell lines

(Submitter supplied) Nucleosomes are important for gene regulation because their arrangement on the genome can control which proteins bind to DNA. Currently, few human nucleosomes are thought to be consistently positioned across cells; however, this has been difficult to assess due to the limited resolution of existing data. We performed paired-end sequencing of micrococcal nuclease-digested chromatin (MNase-seq) from seven lymphoblastoid cell lines and mapped over 3.6 billion MNase-seq fragments to the human genome to create the highest-resolution map of nucleosome occupancy to date in a human cell type. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11154 GPL10999
9 Samples
Download data: TXT, WIG
Series
Accession:
GSE36979
ID:
200036979
9.

Genomewide nucleosome occupancy and DNA methylation analysis on normal and prostate cancer cells

(Submitter supplied) The goal of this study was to compare the nuclosome occupancy and DNA methylation patterns in prostate cancer cells compared to normal prostatic cells
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: BW
Series
Accession:
GSE94361
ID:
200094361
10.

The role of DNA methylation on the organization of the cancer epigenome

(Submitter supplied) We assess global chromatin accessibility following high salt wash
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: BW
Series
Accession:
GSE64929
ID:
200064929
11.

High-resolution nucleosome positioning from ATAC-seq chromatin accessibility data

(Submitter supplied) We describe the NucleoATAC algorithm for high-resolution nucleosome positioning and occupancy determination using ATAC-seq.
Organism:
Schizosaccharomyces pombe; Saccharomyces cerevisiae; Homo sapiens
Type:
Other
4 related Platforms
32 Samples
Download data
Series
Accession:
GSE66386
ID:
200066386
12.

Coordinated Chromatin Remodeling induced by Demethylation requires SRCAP mediated H2A.Z exchange

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by array
Platforms:
GPL6884 GPL8490
12 Samples
Download data
Series
Accession:
GSE26685
ID:
200026685
13.

Coordinated Chromatin Remodeling induced by Demethylation requires SRCAP mediated H2A.Z exchange [expression]

(Submitter supplied) Genome wide gene expression profiling of RKO cells with combination treatments of non-target siRNA or SRCAP siRNA and PBS or 1uM 5-Aza-CdR treatment. The sample treated with non target siRNA and PBS serves as control sample.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6884
8 Samples
Download data: TXT
Series
Accession:
GSE26684
ID:
200026684
14.

Coordinated Chromatin Remodeling induced by Demethylation requires SRCAP mediated H2A.Z exchange [Methylation]

(Submitter supplied) Genome wide DNA methylation profiling of RKO cells with combination treatments of non-target siRNA or SRCAP siRNA and PBS or 1uM 5-Aza-CdR treatment. The Illumina Infinium 27k Human DNA methylation Beadchip v1.2 was used to obtain DNA methylation profiles across 27,578 CpGs in treated RKO cells. Samples included cells under 4 different treatments. The sample treated with non target siRNA and PBS serves as control sample.
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL8490
4 Samples
Download data: TXT
Series
Accession:
GSE26433
ID:
200026433
15.

Large-scale nucleosome density patterns and precise nucleosome positioning correlate with V(D)J recombination at the IgH locus in a cell-type specific manner

(Submitter supplied) In this study, we compare the chromatin structure of the Ig heavy (IgH) chain locus (performing MNase digestion) in three murine cell types rendered recombinationally inactive by loss of a RAG recombinase: (i) RAG2-/- Pro-B cell lines, where the entire IgH locus is poised and available for recombination, (ii) RAG1-/- Pro-T cell lines, lymphoid cells where the IgH locus is partly open but the V region does not rearrange, (iii) recombinationally inactive RAG2-/- mouse embryonic fibroblasts (MEFs), where the entire IgH locus is in a closed conformation and unavailable for rearrangement. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL21139
6 Samples
Download data: PAIR
Series
Accession:
GSE75018
ID:
200075018
16.

Genome-wide positioning of bivalent mononucleosomes

(Submitter supplied) Background: Bivalent chromatin refers to overlapping regions containing activating histone H3 Lys4 trimethylation (H3K4me3) and inactivating H3K27me3 marks. Existence of such bivalent marks on the same nucleosome has only recently been suggested. Previous genome-wide efforts to characterize bivalent chromatin have focused primarily on individual marks to define overlapping zones of bivalency rather than mapping positions of truly bivalent mononucleosomes. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9442
5 Samples
Download data: BED, TXT
Series
Accession:
GSE86838
ID:
200086838
17.

Effects of Histone H3 depletion on nucleosome occupancy and positioning through the S. cerevisiae genome

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL13272
20 Samples
Download data: BED, TXT, WIG
Series
Accession:
GSE29294
ID:
200029294
18.

Effects of Histone H3 depletion on nucleosome occupancy and positioning through the S. cerevisiae genome [RNA_seq]

(Submitter supplied) Experiments performed over the past three decades have shown that nucleosomes are transcriptional repressors. In Saccharomyces cerevisiae, depletion of histone H4 results in the genome-wide transcriptional de-repression of hundreds genes. The mechanism of de-repression is hypothesized to be rooted directly in chromatin changes. To test this, we reproduced classical H4 depletion experiments by conditional repression of all histone H3 transcription, which depletes the supply of nucleosomes in vivo. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13272
6 Samples
Download data: WIG
Series
Accession:
GSE29293
ID:
200029293
19.

Effects of Histone H3 depletion on nucleosome occupancy and positioning through the S. cerevisiae genome [Paired-end Mnase-seq]

(Submitter supplied) Experiments performed over the past three decades have shown that nucleosomes are transcriptional repressors. In Saccharomyces cerevisiae, depletion of histone H4 results in the genome-wide transcriptional de-repression of hundreds genes. The mechanism of de-repression is hypothesized to be rooted directly in chromatin changes. To test this, we reproduced classical H4 depletion experiments by conditional repression of all histone H3 transcription, which depletes the supply of nucleosomes in vivo. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13272
8 Samples
Download data: BED, TXT
Series
Accession:
GSE29292
ID:
200029292
20.

Effects of Histone H3 depletion on nucleosome occupancy and positioning through the S. cerevisiae genome [single-end MNase-seq]

(Submitter supplied) Experiments performed over the past three decades have shown that nucleosomes are transcriptional repressors. In Saccharomyces cerevisiae, depletion of histone H4 results in the genome-wide transcriptional de-repression of hundreds genes. The mechanism of de-repression is hypothesized to be rooted directly in chromatin changes. To test this, we reproduced classical H4 depletion experiments by conditional repression of all histone H3 transcription, which depletes the supply of nucleosomes in vivo. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13272
6 Samples
Download data: BED, TXT
Series
Accession:
GSE29291
ID:
200029291
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