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Items: 12

1.

TSA-Seq Mapping of Nuclear Genome Organization

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Other; Genome binding/occupancy profiling by genome tiling array
4 related Platforms
45 Samples
Download data: PAIR
Series
Accession:
GSE66019
ID:
200066019
2.

TSA-Seq Mapping of Nuclear Genome Organization [array]

(Submitter supplied) We describe TSA-Seq, a new mapping method able to estimate mean chromosomal distances from nuclear speckles genome-wide and predict several Mbp chromosome trajectories between nuclear compartments without sophisticated computational modeling. Ensemble-averaged results reveal a clear nuclear lamina to speckle axis correlated with a striking spatial gradient in genome activity. This gradient represents a convolution of multiple, spatially separated nuclear domains, including two types of transcription "hot-zones". more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
2 Samples
Download data: PAIR
Series
Accession:
GSE66018
ID:
200066018
3.

Massive reshaping of genome - nuclear lamina interactions during oncogene induced senescence (genome tiling)

(Submitter supplied) Background. Cellular senescence is a mechanism that virtually irreversibly suppresses the proliferative capacity of cells in response to various stress signals. This includes the expression of activated oncogenes, which cause Oncogene-Induced Senescence (OIS). A body of evidence points to the involvement of chromatin reorganization, including the formation of senescence-associated heterochromatic foci (SAHF). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
1 Sample
Download data: PAIR
Series
Accession:
GSE76646
ID:
200076646
4.

Massive reshaping of genome - nuclear lamina interactions during oncogene induced senescence

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL11154 GPL10559
37 Samples
Download data: PAIR
Series
Accession:
GSE76605
ID:
200076605
5.

Genome-wide maps of nuclear lamina interactions in single human cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Other; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL11154 GPL10559
411 Samples
Download data: PAIR
Series
Accession:
GSE69423
ID:
200069423
6.

Genome-wide maps of nuclear lamina interactions (DamID on microarray; LaminB1, KBM7 cells, haploid)

(Submitter supplied) Mammalian interphase chromosomes interact with the nuclear lamina (NL) through hundreds of large Lamina Associated Domains (LADs). We report a method to map NL contacts genome-wide in single human cells. Analysis of ~400 maps reveals a core architecture of gene-poor LADs that contact the NL with high cell-to-cell consistency, interspersed by LADs with more variable NL interactions. The variable contacts are more sensitive to a change in genome ploidy than the consistent contacts. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
2 Samples
Download data: PAIR
Series
Accession:
GSE69373
ID:
200069373
7.

Domains of genomewide gene expression dysregulation in Down syndrome

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Methylation profiling by genome tiling array; Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
4 related Platforms
42 Samples
Download data: BW, PAIR, TXT
Series
Accession:
GSE55426
ID:
200055426
8.

Domains of genomewide gene expression dysregulation in Down syndrome [array]

(Submitter supplied) Trisomy 21 (T21) is the most frequent genetic cause of cognitive impairment. To assess the perturbations of gene expression in T21, and to eliminate the noise of the genomic variability, we studied the transcriptome of fetal fibroblasts from a pair of monozygotic twins discordant for T21. Here we show that the differential expression between the twins is organized in domains along all chromosomes that are either up- or downregulated. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL10559
4 Samples
Download data: PAIR, TXT
Series
Accession:
GSE55289
ID:
200055289
9.

Stochastic genome-nuclear lamina interactions: Modulating roles of Lamin A and BAF

(Submitter supplied) The nuclear lamina (NL) is a filamentous layer lining the inner-nuclear-membrane (INM) that aids in the organization of the genome in large domains of low transcriptional activity. Recently, it was shown that the single-cell genome-NL interactions are much more dynamic than previously anticipated, which challenges the concept of the NL as a safe guard for transcriptional repressed genes. Here we discuss the role of the NL in light of these new findings and introduce Lamin A and BAF as potential modulators of LAD positioning
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
4 Samples
Download data: PAIR, TXT
Series
Accession:
GSE55066
ID:
200055066
10.

Stochastic genome - nuclear lamina contacts are linked to histone H3K9 dimethylation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array; Expression profiling by high throughput sequencing
Platforms:
GPL11154 GPL10559
13 Samples
Download data: PAIR
Series
Accession:
GSE40112
ID:
200040112
11.

Stochastic genome - nuclear lamina contacts are linked to histone H3K9 dimethylation (methylation data)

(Submitter supplied) The nuclear lamina (NL) interacts with hundreds of large genomic regions termed lamina-associated domains (LADs). The dynamics of these interactions and the relation to epigenetic modifications are poorly understood. We visualized the fate of LADs in single cells using a novel 'molecular contact memory' approach. In each interphase nucleus, only ~30% of LADs are positioned at the periphery; these LADs are in intermittent molecular contact with the NL but remain constrained to the periphery. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL10559
1 Sample
Download data: PAIR
Series
Accession:
GSE40094
ID:
200040094
12.

Evolutionary conservation of nuclear lamina-genome interactions

(Submitter supplied) Regulation of gene expression is highly conserved between vertebrates, yet the genomic binding patterns of transcription factors are poorly conserved, suggesting that other mechanisms may contribute. The spatial organization of chromosomes in the nucleus is known to affect gene activity, but it is unclear to what extent this organization is conserved in evolution. Genome-wide maps of nuclear lamina (NL) interactions show that human and mouse chromosomes have highly similar folding patterns inside the nucleus. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
6 Samples
Download data: PAIR, TXT
Series
Accession:
GSE22428
ID:
200022428
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