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Links from GEO DataSets

Items: 17

1.

Generation and functional analysis of defective viral genomes during SARS-CoV-2 infection

(Submitter supplied)  In this study, we elucidated defective viral genome generation in SARS-CoV-2 and its relationship with host antiviral immune response. We observed DVGs ubiquitously from RNA-seq datasets of in vitro infections and autopsy lung tissues of COVID-19 patients.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
10 Samples
Download data: TXT
Series
Accession:
GSE222381
ID:
200222381
2.

Defective viral genomes determine respiratory syncytial virus disease severity in adult and children cohorts

(Submitter supplied) Defective viral genomes of the copy-back type (cbDVGs) are generated during RSV infectin and are suggested to impact the clinical outcome. Here in this study we selected the nasal secretions from 13 hospitalized pediatric pateints, including both cnDVG+ and cbDVG-, to perform RNA-seq to understand the impact of cbDVGs on patient transcriptome.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
13 Samples
Download data: TXT
3.

Cell-to-cell variation in defective virus expression and effect on host response during influenza virus infection

(Submitter supplied) Virus and host factors contribute to cell-to-cell variation in viral infection and determine the outcome of the overall infection. However, the extent of the variability at the single cell level and how it impacts virus-host interactions at a systems level are not well understood. To characterize the dynamics of viral transcription and host responses, we used single-cell RNA sequencing to quantify at multiple time points the host and viral transcriptomes of human A549 cells and primary bronchial epithelial cells infected with influenza A virus. more...
Organism:
Homo sapiens; Canis lupus familiaris; Influenza A virus (A/Puerto Rico/8/1934(H1N1))
Type:
Expression profiling by high throughput sequencing; Other
7 related Platforms
33 Samples
Download data: TXT
Series
Accession:
GSE118773
ID:
200118773
4.

Host-virus chimeric events in SARS-CoV2 infected cells are infrequent and artifactual

(Submitter supplied) Pathogenic mechanisms underlying severe SARS-CoV2 infection remain largely unelucidated. High-throughput sequencing technologies that capture genome and transcriptome information are key approaches to gain detailed mechanistic insights from infected cells. These techniques readily detect both pathogen and host-derived sequences, providing a means of studying host-pathogen interactions. Recent studies have reported the presence of host-virus chimeric (HVC) RNA in RNA-seq data from SARS-CoV2 infected cells and interpreted these findings as evidence of viral integration in the human genome as a pathogenic mechanism. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
3 Samples
Download data: TXT
Series
Accession:
GSE167131
ID:
200167131
5.

Replication defective viral products exploit a cellular pro-survival mechanism to establish persistent infections

(Submitter supplied) Replication defective viral genomes (DVGs) generated during virus replication are the primary triggers of antiviral immunity in many infections. However, DVGs also provide viruses with an evolutionary advantage by facilitating virus persistence. Why and how DVGs and the host interact to achieve these two divergent functions remains unknown. We report that DVGs engage a MAVS-mediated antiviral response that promotes apoptosis on highly infected cells while protecting cells dominated by DVGs from death. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
8 Samples
Download data: TXT
6.

Human Nasal Epithelial Cells sustain persistent SARS-CoV-2 infection in vitro, despite eliciting a prolonged antiviral response.

(Submitter supplied) Single Cell Sequencing of SARS-CoV2 Infected Human Nasal Epithelial Cells
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
3 Samples
Download data: MTX, TSV, XLSX
Series
Accession:
GSE182475
ID:
200182475
7.

Genome-wide transcriptome analysis of SARS-CoV-2 positive patients' mucosa, compared with negative controls.

(Submitter supplied) We report the application of genome-wide RNA-sequencing analysis for SARS-CoV-2 positive patients' mucosa. We analyzed the correlation between gene expression levels and viral load (assessed with qPCR) and found a gene signature that might be relevant for diagnosis and treatment of SARS-CoV-2 infection. We performed such analyses in samples with assigned lineage B.1 or B.1.617 (Delta). We compared the expression of these genes in negative patients and observed low abundance, thus confirming their significance.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
342 Samples
Download data: TXT
8.

Expression profiling of SARS-CoV-2 infected patients by RNA-seq

(Submitter supplied) We have collected nasal cell swab samples from SARS-CoV-2 infected confirmed COVID-19 patients. Both virus and host RNA were extracted and sequenced by RNA-seq. We mapped and assembled virus sequences and in this study transcriptional profile of host due to virus infection.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
4 Samples
Download data: TXT
9.

Transcriptome analysis of Severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)-infected and Influenza A/H1N1-infected nasal turbinate and lung tissues

(Submitter supplied) We report the application of RNA sequencing for transcriptome analysis of SARS-CoV-2-infected and Influenza A-infected Human nasal turbinate and lung tissues, enabling the study of tissue responses to viral infections
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
48 Samples
Download data: XLSX
10.

Differential interferon-α immune signatures prevent SARS-CoV-2 infection

(Submitter supplied) Type 1 interferons (IFN-I) exert pleiotropic biological effects during viral infections, balancing virus control and immune-mediated pathology and have been successfully employed for the treatment of viral diseases. In humans, there are twelve IFN-alpha (α) subtypes, which activate downstream signalling cascades and result in a distinct pattern of immune responses and differential antiviral responses. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
60 Samples
Download data: XLSX
Series
Accession:
GSE189613
ID:
200189613
11.

Complete in vivo SHAPE-MaP structure of the SARS-CoV-2 genome

(Submitter supplied) SHAPE-MaP structure probing experiment was performed on SARS-CoV-2 infected Vero cells at 4 days post infection with two biological replicates. For each replciate, SHAPE-MaP includes a sample treated with 2-methylnicotinic acid imidazolide acid (modified) or a minue reagent (unmodified). NAI preferentially reacts with unpaired bases in RNA, forming acylated bases. These modifications are encoded as mutation during reverse transcripatse and library preparation. more...
Organism:
Severe acute respiratory syndrome coronavirus 2
Type:
Other
Platform:
GPL28588
4 Samples
Download data: TXT
Series
Accession:
GSE154171
ID:
200154171
12.

Genome-wide mapping of SARS-CoV-2 RNA structures identifies therapeutically-relevant elements

(Submitter supplied) SARS-CoV-2 is a betacoronavirus with a linear single-stranded, positive-sense RNA genome, whose outbreak caused the ongoing COVID-19 pandemic. The ability of coronaviruses to rapidly evolve, adapt, and cross species barriers makes the development of effective and durable therapeutic strategies a challenging and urgent need. As for other RNA viruses, genomic RNA structures are expected to play crucial roles in several steps of the coronavirus replication cycle. more...
Organism:
Escherichia coli; Severe acute respiratory syndrome coronavirus 2; Chlorocebus sabaeus
Type:
Other
Platforms:
GPL21222 GPL28836 GPL28588
17 Samples
Download data: WIG
Series
Accession:
GSE151327
ID:
200151327
13.

In vivo antiviral host response to SARS-CoV-2 by viral load, sex, and age

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL24676
493 Samples
Download data
Series
Accession:
GSE154770
ID:
200154770
14.

In vivo antiviral host response to SARS-CoV-2 by viral load, sex, and age [dataset III]

(Submitter supplied) We examined host gene expression as a function of time in SARS-CoV-2-infected individuals.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: TXT
Series
Accession:
GSE154769
ID:
200154769
15.

In vivo antiviral host response to SARS-CoV-2 by viral load, sex, and age [dataset II]

(Submitter supplied) We examined host gene expression in human airway epithelial cells following infection at 3 or 7 days post infection (DPI) with SARS-CoV-2
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
3 Samples
Download data: TXT
Series
Accession:
GSE154768
ID:
200154768
16.

In vivo antiviral host response to SARS-CoV-2 by viral load, sex, and age [dataset I]

(Submitter supplied) We examined host gene expression across infection status, viral load, age, and sex among RNA-sequencing profiles of nasopharyngeal swabs from 430 individuals with SARS-CoV-2 and 54 negative controls. SARS-CoV-2 induced a strong interferon-driven antiviral response and reduced transcription of ribosomal proteins. Expression of interferon-responsive genes, including ACE2, increased as a function of viral load. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
484 Samples
Download data: TXT
Series
Accession:
GSE152075
ID:
200152075
17.

Comprehensive mapping of SARS-CoV-2 interactions in vivo reveals virus-snoRNA interactions

(Submitter supplied) SARS-CoV-2 coronavirus is one of the largest RNA viruses (26-32kb) and has emerged as a major threat to global public health. The resulting pandemic has caused global societal and economic disruptions. Here, we investigate the intramolecular and intermolecular RNA interactions of wildtype and a 382 deletion SARS-CoV-2 virus inside cells. We identified twelve potentially functional structural elements along the SARS-CoV-2 genome and observed that subgenomic viral RNA (sgRNAs) contains different structures that could be important for their functions using direct RNA sequencing. more...
Organism:
Chlorocebus
Type:
Other
4 related Platforms
14 Samples
Download data: CSV, TSV
Series
Accession:
GSE165005
ID:
200165005
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