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Items: 1 to 20 of 1567

1.

MHV68 ORF50stop Vaccine Gene Expression

(Submitter supplied) RNA-sequencing from MHV68 ORF50 stop and WT virus infected 3T12 cells (timepoint) post infection.
Organism:
Murid gammaherpesvirus 4; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33263
6 Samples
Download data: FA, GTF, TXT
Series
Accession:
GSE227602
ID:
200227602
2.

Aberrant RNA polymerase Initiation and Processivity on the Genome of a Herpes Simplex Virus 1 Mutant Lacking ICP27

(Submitter supplied) Within the first 15 minutes of infection, herpes simplex virus 1 (HSV-1) immediate early proteins repurpose cellular RNA polymerase (Pol II) for viral transcription. An important role of the viral infected cell protein 27 (ICP27) is to facilitate viral pre-mRNA processing and export of viral mRNA to the cytoplasm. Here, we use precision nuclear run-on followed by deep sequencing (PRO-seq) to characterize transcription of a viral ICP27 null mutant. more...
Organism:
Homo sapiens; Drosophila melanogaster; Human alphaherpesvirus 1
Type:
Other
Platform:
GPL29914
12 Samples
Download data: BW
Series
Accession:
GSE242636
ID:
200242636
3.

Unstable EBV latency drives inflammation in multiple sclerosis patient derived spontaneous B cells [EBV WGS]

(Submitter supplied) Epstein-Barr virus (EBV) is an etiologic risk factor, and likely prerequisite, for the development of multiple sclerosis (MS). However, the role of EBV infected B cells in the immunopathology of MS is not well understood. Here, we characterized spontaneous lymphoblastoid cell lines (SLCLs) isolated from MS patients and healthy controls (HC) ex vivo to study EBV and host gene expression in the context of an individual’s endogenous EBV. more...
Organism:
human gammaherpesvirus 4
Type:
Other
Platform:
GPL34327
9 Samples
Download data: BW, TXT
Series
Accession:
GSE221624
ID:
200221624
4.

A distinct isoform of lymphoid enhancer binding factor 1 (LEF1) epigenetically restricts EBV reactivation to maintain viral latency

(Submitter supplied) As a human tumor virus, EBV is present as a latent infection in its associated malignancies where genetic and epigenetic changes have been shown to impede cellular differentiation and viral reactivation. One such change is increased levels of the Wnt signaling effector, lymphoid enhancer binding factor 1 (LEF1) following EBV epithelial infection. In silico analysis of EBV type 1 and 2 genomes identified over 20 Wnt-response elements suggesting that LEF1 may directly bind the EBV genome and regulate the viral life cycle. more...
Organism:
human gammaherpesvirus 4
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL33849 GPL33850
31 Samples
Download data: BEDGRAPH
Series
Accession:
GSE245534
ID:
200245534
5.

The three-dimensional structure of the EBV genome plays a crucial role in regulating viral gene expression in EBVaGC [RNA-seq]

(Submitter supplied) Epstein-Barr virus (EBV) establishes lifelong asymptomatic infection by replication of its chromatinized episomes with the host genome. EBV exhibits different latency-associated transcriptional repertoires, each with distinct three-dimensional structures. CTCF, Cohesin and PARP1 are involved in maintaining viral latency and establishing episome architecture. Epstein-Barr virus-associated gastric cancer (EBVaGC) represents 1.3% to 30.9% of all gastric cancers globally. more...
Organism:
human gammaherpesvirus 4; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23185
3 Samples
Download data: TXT
Series
Accession:
GSE239994
ID:
200239994
6.

The three-dimensional structure of the EBV genome plays a crucial role in regulating viral gene expression in EBVaGC [HiChIP]

(Submitter supplied) Epstein-Barr virus (EBV) establishes lifelong asymptomatic infection by replication of its chromatinized episomes with the host genome. EBV exhibits different latency-associated transcriptional repertoires, each with distinct three-dimensional structures. CTCF, Cohesin and PARP1 are involved in maintaining viral latency and establishing episome architecture. Epstein-Barr virus-associated gastric cancer (EBVaGC) represents 1.3% to 30.9% of all gastric cancers globally. more...
Organism:
human gammaherpesvirus 4; Homo sapiens
Type:
Other
Platform:
GPL23185
4 Samples
Download data: BEDPE, TXT
Series
Accession:
GSE239992
ID:
200239992
7.

The three-dimensional structure of the EBV genome plays a crucial role in regulating viral gene expression in EBVaGC [HiC]

(Submitter supplied) Epstein-Barr virus (EBV) establishes lifelong asymptomatic infection by replication of its chromatinized episomes with the host genome. EBV exhibits different latency-associated transcriptional repertoires, each with distinct three-dimensional structures. CTCF, Cohesin and PARP1 are involved in maintaining viral latency and establishing episome architecture. Epstein-Barr virus-associated gastric cancer (EBVaGC) represents 1.3% to 30.9% of all gastric cancers globally. more...
Organism:
human gammaherpesvirus 4
Type:
Other
Platform:
GPL25190
10 Samples
Download data: TXT
Series
Accession:
GSE239989
ID:
200239989
8.

The three-dimensional structure of the EBV genome plays a crucial role in regulating viral gene expression in EBVaGC [ChIP-seq]

(Submitter supplied) Epstein-Barr virus (EBV) establishes lifelong asymptomatic infection by replication of its chromatinized episomes with the host genome. EBV exhibits different latency-associated transcriptional repertoires, each with distinct three-dimensional structures. CTCF, Cohesin and PARP1 are involved in maintaining viral latency and establishing episome architecture. Epstein-Barr virus-associated gastric cancer (EBVaGC) represents 1.3% to 30.9% of all gastric cancers globally. more...
Organism:
human gammaherpesvirus 4
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25190
12 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE239987
ID:
200239987
9.

ac4C-seq of cellular and KSHV transcripts in iSLK-Puro, iSLK-KSHV (i.e. iSLK-RGB), iSLK-KSHV (WT), iSLK-KSHV (ΔNAT10) cells

(Submitter supplied) We used ac4C-seq to detedc cellular and KSHV transcripts in iSLK-Puro, iSLK-KSHV, iSLK-KSHV (WT), iSLK-KSHV (ΔNAT10) cells after after doxycycline and sodium butyrate treatment.
Organism:
Human gammaherpesvirus 8; Homo sapiens
Type:
Other
Platform:
GPL30065
24 Samples
Download data: TXT, XLS
Series
Accession:
GSE174161
ID:
200174161
10.

RIP-seq of NAT10 interacted cellular and KSHV transcripts in iSLK-KSHV cells

(Submitter supplied) Flag-RIP-seq was performed in NAT10-Flag overexpressing iSLK-KSHV cells.
Organism:
Homo sapiens; Human gammaherpesvirus 8
Type:
Other
Platform:
GPL30065
12 Samples
Download data: TXT
Series
Accession:
GSE173889
ID:
200173889
11.

m6A modification of EBV transcripts

(Submitter supplied) We examined the viral epitranscriptome in EBV transformed lymphoblastoid cell lines (LcLs) and EBV-positive Burkitt's lymphoma, Akata cells, using methylated RNA immunoprecipitation followed by sequencing (MeRIP-seq). Biological replicates of ribo-RNA deleted mRNA of each cell type were prepared for MeRIP-seq followed by peak calling using the exome Peak package with settings for stringent peak calling on both strands of the genome.
Organism:
human gammaherpesvirus 4
Type:
Other
Platform:
GPL26377
16 Samples
Download data: CSV, TXT
Series
Accession:
GSE129217
ID:
200129217
12.

Decitabine disrupts EBV genomic epiallele DNA methylation patterns around CTCF binding sites to increase chromatin accessibility and lytic transcription in gastric cancer [ChIP-seq]

(Submitter supplied) To investigate the EBV genome after Decitabine treatment by CTCF ChIP-seq
Organism:
human gammaherpesvirus 4
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL33481
8 Samples
Download data: BW
Series
Accession:
GSE234603
ID:
200234603
13.

Decitabine disrupts EBV genomic epiallele DNA methylation patterns around CTCF binding sites to increase chromatin accessibility and lytic transcription in gastric cancer [RNA]

(Submitter supplied) To investigate the EBV genome after Decitabine treatment by reduced representation bisulfite sequencing, ATAC-seq, and RNA-seq
Organism:
human gammaherpesvirus 4
Type:
Expression profiling by high throughput sequencing
Platform:
GPL25190
18 Samples
Download data: BW, TXT
Series
Accession:
GSE239767
ID:
200239767
14.

Decitabine disrupts EBV genomic epiallele DNA methylation patterns around CTCF binding sites to increase chromatin accessibility and lytic transcription in gastric cancer [ATAC]

(Submitter supplied) To investigate the EBV genome after Decitabine treatment by reduced representation bisulfite sequencing, ATAC-seq, and RNA-seq
Organism:
human gammaherpesvirus 4
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL33481
12 Samples
Download data: BW
Series
Accession:
GSE239645
ID:
200239645
15.

HSV-1 exploits host heterochromatin for egress [CUT&Tag]

(Submitter supplied) Herpes simplex virus replicates and forms progeny in the nucleus where it must overcome host chromatin to establish a successful infection. During lytic infection, newly formed viral capsids navigate through heterochromatin channels at the nuclear periphery to egress out of the nucleus. In uninfected cells, specific histone marks such as trimethylation on histone H3 lysine 27 (H3K27me3) and the histone variant macroH2A1 delineate heterochromatin regions, or repressed chromatin, that are predominantly located in the nuclear periphery. more...
Organism:
Homo sapiens; Human alphaherpesvirus 1
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL23890
48 Samples
Download data: BW
Series
Accession:
GSE208127
ID:
200208127
16.

Decitabine disrupts EBV genomic epiallele DNA methylation patterns around CTCF binding sites to increase chromatin accessibility and lytic transcription in gastric cancer [RRBS]

(Submitter supplied) To investigate the EBV genome after Decitabine treatment by reduced representation bisulfite sequencing, ATAC-seq, and RNA-seq
Organism:
human gammaherpesvirus 4
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL25190
8 Samples
Download data: COV
Series
Accession:
GSE233330
ID:
200233330
17.

Single-Cell Transcriptomics of Epstein-Barr Virus and Human Herpesvirus 6 Coinfection

(Submitter supplied) Epstein-Barr virus (EBV) and human herpesvirus 6 (HHV-6) infection is widespread among people. Here I describe single-cell RNA sequencing of two lymphoblastoid cell lines harboring both episomal EBV and inherited chromosomally integrated HHV-6. Rare instances of HHV-6 expression appear enriched with EBV reactivation.
Organism:
human gammaherpesvirus 4; Human betaherpesvirus 6B; Homo sapiens; Human betaherpesvirus 6A
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL33373 GPL33355
2 Samples
Download data: H5
Series
Accession:
GSE230239
ID:
200230239
18.

Rat cytomegalovirus efficiently replicates within dendritic cells and affects both surface marker and gene expression

(Submitter supplied) Dendritic cells (DC) play a crucial role in generating and maintaining antiviral immunity. While DC are implicated in the antiviral defense by inducing T cell responses, they can also become infected by Cytomegalovirus (CMV). CMV is not only highly species-specific but also specialized in evading immune protection, and this specialization is in part due to characteristic genes encoded by a given virus. more...
Organism:
Rattus norvegicus; Murid betaherpesvirus 8
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL22396 GPL34220
15 Samples
Download data: TSV
Series
Accession:
GSE232184
ID:
200232184
19.

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
20.

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
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