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Links from GEO DataSets

Items: 15

1.

HCMV infected Human Fibroblasts UL84 IE2 ChIPSeq

(Submitter supplied) We report ChIP-seq analsyis of human fibroblasts infected with HCMV strains AD169 and TB40E. ChIP was performed at 20 hpi for IE2 and 3 dpi for IE2 and UL84.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: WIG
Series
Accession:
GSE169634
ID:
200169634
2.

ChIP-seq targeting Myc-tagged UL34 from human fibroblasts infected with human cytomegalovirus at 48 hours post infection

(Submitter supplied) Purpose: To identify interactions of the viral DNA-binding protein, UL34, with the viral genome during lytic-phase replication. Methods: Human fibroblasts were infected with human cytomegalovirus expressing Myc-tagged UL34 in biological duplicate. At 48 hours post infection, ChIP was performed with anti-Myc tag antibody (Cell Signaling) and the resulting DNA fragments were sequenced on Illumina MiSeq. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15520
4 Samples
Download data: TXT
Series
Accession:
GSE106211
ID:
200106211
3.

Human cytomegalovirus IE2 both activates and represses initiation and modulates elongation in a context-dependent manner

(Submitter supplied) Using PRO-Seq, which profiles nascent transcripts, and a recently developed DFF-ChIP approach that informs on local chromatin environment, we show that IE2 controls viral gene transcription in three distinct capacities during late HCMV infection and reveal mechanisms involving direct binding of IE2 to viral DNA. IE2 represses a subset of viral promoters by binding within the target core promoter region, blocking the assembly preinitiation complexes (PICs). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24676
14 Samples
Download data: BW
Series
Accession:
GSE193026
ID:
200193026
4.

Differences in RNA polymerase II complexes and their interactions with surrounding chromatin on human and cytomegalovirus genomes

(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
Platforms:
GPL24676 GPL20301
38 Samples
Download data: BW
Series
Accession:
GSE185763
ID:
200185763
5.

Differences in RNA polymerase II complexes and their interactions with surrounding chromatin on human and cytomegalovirus genomes [ChIP-seq]

(Submitter supplied) To investigate the chromatin structure surrounding human RNA polymerase II (Pol II) transcription on host and viral genomes, chromatin immunoprecipitation (ChIP) was performed following digestion of HCMV infected primary human foreskin fibroblasts (HFFs) with DNA Fragmentation Factor (DFF). DFF is a human endonuclease responsible for cleaving between nucleosomes during apoptosis. We found that utilizing DFF as the front end for ChIP-Seq in place of sonication or Micrococcal nuclease (MNase) offered new insights into the connections between active transcription and the local chromatin on the host and that these connections were completely absent on the HCMV genome.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24676 GPL20301
25 Samples
Download data: BW
Series
Accession:
GSE185618
ID:
200185618
6.

Human cytomegalovirus IE2 drives transcription initiation from a select subset of late infection viral promoters by host RNA polymerase II

(Submitter supplied) Herpesvirus late promoters activate gene expression after viral DNA synthesis has begun. Alphaherpesviruses utilize a viral immediate-early protein to do this, whereas beta- and gammaherpesviruses primarily use a 6-member set of viral late-acting transcription factors (LTF) that are drawn to a TATT sequence in the late promoter. The betaherpesvirus, human cytomegalovirus (HCMV), produces three immediate-early 2 protein isoforms, IE2-86, IE2-60, IE2-40, in late infection, but whether they activate late viral promoters is unknown. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20301
22 Samples
Download data: BED, BW
Series
Accession:
GSE139114
ID:
200139114
7.

Human cytomegalovirus long noncoding RNA4.9 regulates viral DNA replication

(Submitter supplied) Viruses are known for their extremely compact genomes composed almost entirely of protein-coding genes. Nonetheless, four long noncoding RNAs (lncRNAs) are encoded by human cytomegalovirus (HCMV). Although these RNAs accumulate to high levels during lytic infection, their functions remain largely unknown. Here, we show that HCMV-encoded lncRNA4.9 localizes to the viral nuclear replication compartment, and that its depletion restricts viral DNA replication and viral growth. more...
Organism:
Murid betaherpesvirus 1; Homo sapiens; Human betaherpesvirus 5; Mus musculus
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL24958 GPL26926
5 Samples
Download data: XLSX
Series
Accession:
GSE134423
ID:
200134423
8.

HCMV epigenome and transcriptome during early lytic infection

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Human betaherpesvirus 5
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL29977 GPL24676
25 Samples
Download data: BIGWIG
Series
Accession:
GSE171522
ID:
200171522
9.

Role of the HCMV immediate early proteins in controlling the HCMV transcriptome

(Submitter supplied) Purpose: to investigate the role of the HCMV immediate early genes in controlling the HCMV and cellular transcriptomes
Organism:
Homo sapiens; Human betaherpesvirus 5
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29977
4 Samples
Download data: BIGWIG
Series
Accession:
GSE171521
ID:
200171521
10.

HCMV transcriptome during early lytic infection

(Submitter supplied) Purpose: to investigate expression of HCMV and cellular RNAs at early times post-infection in a lytic model
Organism:
Human betaherpesvirus 5; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29977
2 Samples
Download data: BIGWIG
Series
Accession:
GSE171520
ID:
200171520
11.

Transcriptome of MRC5 fibroblasts

(Submitter supplied) Purpose: to investigate the human transcriptome in MRC5 fibroblasts
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
3 Samples
Download data: BIGWIG
12.

Role of the HCMV immediate early proteins in controlling the HCMV and cellular epigenomes

(Submitter supplied) Purpose: to investigate the role of the HCMV immediate early proteins in controlling the HCMV and cellular epigneomes during lytic infectioin
Organism:
Homo sapiens; Human betaherpesvirus 5
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL29977
16 Samples
Download data: BIGWIG
Series
Accession:
GSE171518
ID:
200171518
13.

HCMV epigenome during early lytic infection

(Submitter supplied) Purpose: to investigate occupancy of Pol II and H3K27Ac on the HCMV and cellular genomes at early times post-infection in a lytic model
Organism:
Human betaherpesvirus 5; Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL29977
8 Samples
Download data: BIGWIG
Series
Accession:
GSE171512
ID:
200171512
14.

Pol II and H3K27Ac occupancy of the human genome in MRC5 cells

(Submitter supplied) Purpose: to investigate the epigeome of MRC5 fibroblasts
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24676
12 Samples
Download data: BIGWIG
Series
Accession:
GSE171509
ID:
200171509
15.

Nucleotide resolution of RNA polymerase II transcription in human cytomegalovirus

(Submitter supplied) We performed paired-end PRO-Seq and/or PRO-Cap on human foreskin fibroblasts (HFF) infected with human cytomegalovirus (HCMV) for 4 h (strain TB40/E) or 96 h (strain Towne varS). Each sample has matched uninfected controls. Towne experiments were also performed with adapters containing 4 nt of random sequence flanking both sides (8 total bases of randomness) to enable deduplication. Reads were first mapped to the human genome (hg38) (files available on GEO). more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL20301
13 Samples
Download data: BB, BW
Series
Accession:
GSE113394
ID:
200113394
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