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Links from GEO DataSets

Items: 20

1.

MNase-chip of maize B73 immature ears and seedlings

(Submitter supplied) The eukaryotic nuclear genome is organized into the fundamental units of chromatin, nucleosomes. The positions and biochemical states of nucleosomes on DNA can regulate protein-DNA interactions, and in turn influence DNA-templated events. Despite the increasing number of genome-wide maps of nucleosome position, how global changes in nucleosome position relate to changes in gene expression is poorly understood. more...
Organism:
Zea mays
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL19042
24 Samples
Download data: PAIR, TSV
Series
Accession:
GSE60090
ID:
200060090
2.

MNase-chip of maize B73

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Zea mays
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL19041 GPL19042
34 Samples
Download data: PAIR
Series
Accession:
GSE60092
ID:
200060092
3.

MNase-chip of maize B73 immature ears, seedling shoots, and seedling roots

(Submitter supplied) The eukaryotic nuclear genome is organized into the fundamental units of chromatin, nucleosomes. The positions and biochemical states of nucleosomes on DNA can regulate protein-DNA interactions, and in turn influence DNA-templated events. Despite the increasing number of genome-wide maps of nucleosome position, how global changes in nucleosome position relate to changes in gene expression is poorly understood. more...
Organism:
Zea mays
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL19041
10 Samples
Download data: PAIR, TSV
Series
Accession:
GSE60089
ID:
200060089
4.

Subtracting the sequence bias from partially digested MNase-seq data reveals a general contribution of TFIIS to nucleosome dynamics

(Submitter supplied) Understanding chromatin dynamics is a key to other related processes, including DNA replication, transcription and recombination. As a first step, recently, an increasing amount of effort has been devoted to precisely define nucleosome positioning in different organisms. The most popular method to do so is digestion by Micrococcal nuclease (MNase), nowadays followed by ultrasequencing of the generated fragments. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13821 GPL13272
3 Samples
Download data: BED
Series
Accession:
GSE94313
ID:
200094313
5.

Chromatin-dependent regulation of the RNA polymerases II and III activity throughout the transcription cycle

(Submitter supplied) We have developed a new genome-wide protocol for nascent transcription analysis at high resolution in the yeast Saccharomyces cerevisiae. This protocol is based in run-on labeling of nascent RNA with a biotinylated precursor. We call it BioGRO for biotin-based genomic run-on.
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by genome tiling array; Genome binding/occupancy profiling by genome tiling array
Platform:
GPL18871
7 Samples
Download data: BAR, CEL, TXT
Series
Accession:
GSE58859
ID:
200058859
6.

Genomic Run On (GRO): determination of the nascent transcriptional rates and mRNA levels in several yeast mutants.

(Submitter supplied) In order to maintain the appropriate level of mRNA it is necessary coordinate simultaneously all the steps along the mRNA life cycle. It has been shown that several factors act in the regulation of gene expression as global coordinators. Thus, some kind of information is transferred from the nucleus to the cytoplasm, imprinted in the mRNA. In this way, it is conceivable the existence of mechanisms that ensure the balance between mRNA synthesis and degradation through the information flow from the cytoplasm to the nucleus and vice versa, as a crosstalk among both process to ensure the proper mRNA homeostasis in the cell. more...
Organism:
Saccharomyces cerevisiae
Type:
Expression profiling by array
Platform:
GPL13620
18 Samples
Download data: TXT
Series
Accession:
GSE57467
ID:
200057467
7.

Asymmetric nucleosomes flank promoters in the budding yeast genome

(Submitter supplied) Nucleosomes in active chromatin are dynamic, but whether they have distinct structural conformations is unknown. To identify nucleosomes with alternative structures genome-wide, we used H4S47C-anchored cleavage mapping, which revealed that nucleosomes at 5% of budding yeast nucleosome positions have asymmetric histone-DNA interactions. These asymmetric interactions are enriched at nucleosome positions that flank promoters. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL17342 GPL13821
17 Samples
Download data: BED
Series
Accession:
GSE59523
ID:
200059523
8.

Genome-wide chromatin mapping with size resolution reveals a dynamic sub-nucleosomal landscape in Arabidopsis

(Submitter supplied) Background: Analysis of the effect that chromatin structure has on the expression patterns of eukaryotic genes has recently expanded knowledge of the complex influence genome accessibility has on genome function. Interlaced with regular nucleosomal patterning are other mobile and labile sub-nucleosomal-sized protein structures bound to the genome such as transcription factors (TF), initiation complexes, and modified nucleosomes. more...
Organism:
Arabidopsis thaliana
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL17639
16 Samples
Download data: CSV, WIG
Series
Accession:
GSE94377
ID:
200094377
9.

MNase sensitivity of promoter chromatin in GM12878 cells during stimulation with heat-killed Salmonella typhimurium

(Submitter supplied) We employed an MNase-Transcription Start Site Sequence Capture method to map and determine the accessibility of all nucleosomes during immune stimulus, at high coverage for all human Pol II promoters. We uncovered features of nucleosomal organization and sensitivity to MNase digestion in B-lymphoblastoid cells. We also find that transcription factor binding is associated with sensitive nucleosomes.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
16 Samples
Download data: TXT
Series
Accession:
GSE139224
ID:
200139224
10.

Differential features of lamina-associated domains mapped by ChIP-sequencing from sonicated or micrococcal nuclease-digested chromatin

(Submitter supplied) The nuclear lamina interacts with the genome through megabase-size lamina-associated domains (LADs). LADs have been identified in proximity labeling assays and recently by chromatin immunoprecipitation-sequencing (ChIP-seq) of A- and B-type lamins. LADs localize mainly to the nuclear periphery, they are gene-poor and largely heterochromatic. Here, we show that the mode of chromatin fragmentation for ChIP, namely either bath sonication (used to date for ChIP of nuclear lamins) or digestion with micrococcal nuclease (MNase) leads to the discovery of distinct sets of lamin-interacting domains (which we refer to as LiDs) with distinct gene content, histone composition enrichment and relationship to lamin B1-interacting domains. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
5 Samples
Download data: BED
Series
Accession:
GSE57149
ID:
200057149
11.

EDD: a program for detection of wide genomic enrichment domains robust against local variations

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL16791
7 Samples
Download data: BED, CSV
Series
Accession:
GSE54334
ID:
200054334
12.

EDD: a program for detection of wide genomic enrichment domains robust against local variations [RNA-Seq]

(Submitter supplied) Nuclear lamins contact the genome at the nuclear periphery through large domains and are involved in chromatin organization. Among broad peak calling algorithms available to date, none are suited for mapping lamin-genome interactions genome-wide. We disclose a novel algorithm, Enriched Domain Detector (EDD), for analysis of broad enrichment domains from ChIP-seq data. EDD enables discovery of genomic domains interacting with broadly distributed chromatin-associated proteins such as lamins. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
2 Samples
Download data: CSV
13.

EDD: a program for detection of wide genomic enrichment domains robust against local variations [ChIP-Seq]

(Submitter supplied) Nuclear lamins contact the genome at the nuclear periphery through large domains and are involved in chromatin organization. Among broad peak calling algorithms available to date, none are suited for mapping lamin-genome interactions genome-wide. We disclose a novel algorithm, Enriched Domain Detector (EDD), for analysis of broad enrichment domains from ChIP-seq data. EDD enables discovery of genomic domains interacting with broadly distributed chromatin-associated proteins such as lamins. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
5 Samples
Download data: BED
Series
Accession:
GSE54332
ID:
200054332
14.

The regulatory landscape of early maize inflorescence development

(Submitter supplied) The functional genome of agronomically important plant species remains largely unexplored, yet presents a virtually untapped resource for targeted crop improvement. Functional elements and regulatory DNA revealed through chromatin accessibility maps can be harnessed for manipulating gene expression to subtle phenotypic outputs that enhance productivity in specific environments. Here, we present a genome-wide view of accessible chromatin and nucleosome occupancy at a very early stage in the development of both pollen- and grain-bearing inflorescences of the important cereal crop maize (Zea mays), using an assay for differential sensitivity of chromatin to micrococcal nuclease (MNase) digestion. more...
Organism:
Zea mays
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17628
8 Samples
Download data: BED, BW, TXT, ZIP
Series
Accession:
GSE136685
ID:
200136685
15.

Widespread changes in nucleosome accessibility without changes in nucleosome occupancy during a rapid transcriptional induction

(Submitter supplied) Activation of transcription requires alteration of chromatin by complexes that increase the accessibility of nucleosomal DNA. Removing nucleosomes from regulatory sequences has been proposed to play a significant role in activation. We tested whether changes in nucleosome occupancy occurred on the set of genes that are activated by the unfolded protein response (UPR). We observed no decrease in occupancy on most promoters, gene bodies, and enhancers. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL13304 GPL17275
64 Samples
Download data: BEDGRAPH
Series
Accession:
GSE95689
ID:
200095689
16.

MNase-seq analysis of Col-0 and chr11-1 chr17-1

(Submitter supplied) Chromatin has a highly organized structure with the repeating nucleosome subunits. The position of nucleosomes on the chromatin is dynamically regulated by ATP-dependent chromatin remodeling factors (remodelers), therefore providing specific epigenetic information. However, the in vivo nucleosome distribution pattern in plants and how plant remodelers control the pattern formation are not yet clear. more...
Organism:
Arabidopsis thaliana
Type:
Other
Platform:
GPL17639
2 Samples
Download data: WIG
Series
Accession:
GSE50242
ID:
200050242
17.

Genome-wide DNase-seq profiling of Saccharomyces cerevisiae (W303 strain)

(Submitter supplied) Intact nuclei from an asynchronous population of W303 Saccharomyces cerevisiae in log-phase growth were subjected to a 16-minute DNase I digestion (0.1 U/μL) at 37 °C. DNA was then recovered, and single-end Illumina sequencing libraries were prepared using the Crawford DNase-seq method (Song and Crawford, 2010).
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13821
2 Samples
Download data: CSV
Series
Accession:
GSE69651
ID:
200069651
18.

scMNase-seq measures chromatin accessibility and nucleosome positioning in single cells

(Submitter supplied) Nucleosome positioning is critical to chromatin accessibility, and is associated with gene expression programs in cells. Previous nucleosome mapping methods assemble profiles from cell populations and reveal a cell-averaged pattern: nucleosomes are positioned and form a phased array surrounding the transcription start sites (TSSs ) of active genes and DNase I hypersensitive sites (DHSs). However, cells exhibit remarkable expression heterogeneity in response to active signaling even in a homogenous population of cells, which may be related to the heterogeneity in chromatin accessibility. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
586 Samples
Download data: BED
Series
Accession:
GSE96688
ID:
200096688
19.

Genome-wide characterization of cis-acting DNA targets of Opaque2 in maize

(Submitter supplied) Opaque2 (O2) is a transcription factor that plays important roles during maize endosperm development. Mutation of the O2 gene improves the nutritional value of maize seeds, but also confers pleiotropic effects that result in reduced agronomic quality. To reveal the transcriptional regulatory framework of O2, we determined O2 DNA binding targets using chromatin immunoprecipitation coupled to high-throughput sequencing (ChIP-Seq). more...
Organism:
Zea mays
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15463
2 Samples
Download data: BED, TXT
Series
Accession:
GSE63991
ID:
200063991
20.

Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and opaque2 mutant Transcriptomes

(Submitter supplied) Analysis of gene expression level. The hypothesis tested in the present study was that opaque2 mutant influence the expression of storage proteins. Results provide important information of the gene expression level regulation of storage proteins and other biological processes.
Organism:
Zea mays
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17628
2 Samples
Download data: TXT
Series
Accession:
GSE61830
ID:
200061830
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