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Links from GEO DataSets

Items: 20

1.

Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and Nrl-/- Retinal Transcriptomes

(Submitter supplied) Purpose: Next-generation sequencing (NGS) has revolutionized systems-based analysis of cellular pathways. The goals of this study are to compare NGS-derived retinal transcriptome profiling (RNA-seq) to microarray and quantitative reverse transcription polymerase chain reaction (qRT–PCR) methods and to evaluate protocols for optimal high-throughput data analysis. Methods: Retinal mRNA profiles of 21-day-old wild-type (WT) and neural retina leucine zipper knockout (Nrl−/−) mice were generated by deep sequencing, in triplicate, using Illumina GAIIx. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
6 Samples
Download data: BAM, TXT, XLS
Series
Accession:
GSE33141
ID:
200033141
2.

RNA sequencing profiling of the retina in C57BL/6J and DBA/2J mice: enhancing the retinal microarray datasets from GeneNetwork

(Submitter supplied) Purpose: The goal of the present study is to provide an independent assessment of the retinal transcriptome signatures of the C57BL/6J (B6) and DBA/2J (D2) mice and to enhance existing microarray datasets for accurately defining the allelic differences in the BXD recombinant inbred strains. Methods: Retinas from both B6 and D2 mice (3 of each) were used for the RNA-seq analysis. Transcriptome features were examined for both strains. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: TXT, XLSX
Series
Accession:
GSE127942
ID:
200127942
3.

Expression profiling of the developing and mature Nrl -/- mouse retina (Yoshida et al. 2004, HMG)

(Submitter supplied) The rod photoreceptor-specific neural retina leucine zipper protein Nrl is essential for rod differentiation and plays a critical role in regulating gene expression. In the mouse retina, rods account for 97% of the photoreceptors; however, in the absence of Nrl (Nrl-/-), no rods are present and a concomitant increase in cones is observed. Using mouse GeneChips (Affymetrix), we have generated expression profiles of the wild-type and Nrl-/- retina at three time-points representing distinct stages of photoreceptor differentiation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2936
Platform:
GPL81
24 Samples
Download data: CEL
Series
Accession:
GSE8972
ID:
200008972
4.
Full record GDS2936

Neural retina leucine zipper deficiency effect on retinas: time course

Analysis of retinas of mutants lacking the rod photoreceptor-specific neural retina leucine zipper protein (Nrl), at up to 2 months of age. In the absence of Nrl, rods are missing and cones increase in number. Results provide insight into the differences between the two photoreceptor subtypes.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 age, 2 genotype/variation sets
Platform:
GPL81
Series:
GSE8972
24 Samples
Download data: CEL
DataSet
Accession:
GDS2936
ID:
2936
5.

NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors.

(Submitter supplied) Gene regulatory networks (GRNs) guiding differentiation of cell types and cell assemblies in the nervous system are poorly understood because of inherent complexities and interdependence of signaling pathways. Here, we report transcriptome dynamics of differentiating rod photoreceptors in the mammalian retina. Given that the transcription factor NRL determines rod cell fate, we performed expression profiling of developing NRL-positive (rods) and NRL-negative (S-cone-like) mouse photoreceptors. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6096
28 Samples
Download data: CEL
Series
Accession:
GSE74657
ID:
200074657
6.

Retinal gene expression in Egr-1 knock-out mice during development (p30 and p42)

(Submitter supplied) In chicks, the avian homologue of the early growth response protein-1 (ZENK) has been shown to be increased in a special cell type of the retina, the glucagonergic amacrine cells, under conditions that lead to a reduction in eye growth (myopic defocus, recovery of myopia) and decreased under conditions that enhance ocular growth (hyperopic defocus, form-deprivation). The investigation of Egr-1 knock-out mice showed that homozygous knock-out mice with no functional Egr-1 protein developed relative axial myopia at the age of 42 and 56 days, compared to heterozygous- and wildtype Egr-1 knock-out mice. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS3607
Platform:
GPL1261
16 Samples
Download data: CEL
Series
Accession:
GSE16974
ID:
200016974
7.
Full record GDS3607

Egr-1 deficiency effect on retina during eye development

Analysis of retinas of Egr-1 deficient animals at post-natal days 30 and 42. 42 day-old Egr-1 knockout animals have longer eyes and a more myopic refractive error compared to wild-types. Results provide insight into the molecular mechanisms regulating axial eye growth.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 age, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE16974
16 Samples
Download data: CEL
8.

Evaluating Gene Expression in C57BL/6J and DBA/2J Mouse Striatum Using RNA-Seq and Microarray

(Submitter supplied) C57BL/6J (B6) and DBA/2J (D2) are two of the most commonly used inbred mouse strains in neuroscience research. However, the only currently available mouse genome is based entirely on the B6 strain sequence. Subsequently, oligonucleotide microarray probes are based solely on this B6 reference sequence, making their application for gene expression profiling comparisons across mouse strains dubious due to their allelic sequence differences, including single nucleotide polymorphisms (SNPs). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL6885 GPL1261
44 Samples
Download data: CEL, TXT
Series
Accession:
GSE26024
ID:
200026024
9.

Transcript assembly and abundance estimation from RNA-Seq reveals thousands of new transcripts and switching among isoforms

(Submitter supplied) We introduce an approach to transcript discovery coupled with a statistical model for RNA-Seq experiments that produces estimates of transcript abundances. Our algorithms are implemented in an open source software program called Cufflinks. To test Cufflinks, we sequenced and analyzed more than 430 million paired 75bp RNA-Seq reads from a mouse myoblast cell line representing a differentiation timeseries. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9185
4 Samples
Download data: GTF, SAM
Series
Accession:
GSE20846
ID:
200020846
10.

Human Large Airway Epithelial Cells from healthy never and current smoker and smokers with and without lung cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL13447 GPL10999
21 Samples
Download data: BEDGRAPH, CEL, TXT
Series
Accession:
GSE29007
ID:
200029007
11.

mRNA-seq of Human Airway Epithelial Cells

(Submitter supplied) mRNA expression was profiled from pooled bronchial airway epithelial cell brushings (n=3 patients/pool) obtained during bronchoscopy from healthy never (NS) and current smokers (S) and smokers with (C) and without (NC) lung cancer
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10999
8 Samples
Download data: BEDGRAPH, GTF, TXT
12.

Large airway epithelial cells from cigarette smokers with and without lung cancer undergoing flexible bronchoscopy in the operating room for resection of a suspicious lung nodule

(Submitter supplied) mRNA expression was assayed from bronchial epithelial cell samples from smokers with and without lung cancer. A subset of the samples (2 of the lung cancer samples and 3 of the no cancer samples) were pooled and underwent whole transcriptome sequencing. The goals were to compare whole transcriptome sequencing gene expression levels to gene expression levels derived from these samples run on the Affymetrix HGU133A 2.0 platform.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13447
13 Samples
Download data: CEL
Series
Accession:
GSE28835
ID:
200028835
13.

RNA-sequencing study of peripheral blood monocytes for chronic periodontitis

(Submitter supplied) We confirmed immune response as the key mechanism and provided solid evidence for novel genes (e.g., FCAR and CUX1) and distinct biological processes (e.g., endocytosis, cytokine production and apoptosis) as potentially new important factors/mechanisms contributing to chronic periodontitis pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
10 Samples
Download data: CSV
14.

Evaluation of the post-stroke transcriptome of the mouse cortex using genome-wide RNA-seq

(Submitter supplied) RNA-sequencing was conducted to profile the transcriptome of the post-ischemic mouse cortex at multiple reperfusion time-points. RNA was isolated from sham and middle cerebral artery occlusion (MCAO)-operated mice at different reperfusion time points (6 h, 12 h or 24 h; three independent biological replicates per group), converted into cDNA libraries, and used for Illumina deep sequencing on a NexSeq500 instrument. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: GTF
Series
Accession:
GSE112348
ID:
200112348
15.

A Systematic Comparison and Evaluation of High Density Exon Arrays and RNA-seq technology in Unraveling the Peripheral Blood Transcriptome of Sickle Cell Disease.

(Submitter supplied) Sickle cell transcriptome was analyzed using whole blood clinical specimens on the Affymetrix Human Exon 1.0 ST arrays and Illumina’s deep sequencing technologies. Data analysis indicated a strong concordance (R=0.64) between exon array and RNA-seq in both gene level and exon level expression of transcripts. The magnitude of fold changes in the expression levels for the differentially expressed genes (p<0.05) was found to be higher in RNA-seq than microarrays. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5188
10 Samples
Download data: CEL
Series
Accession:
GSE31757
ID:
200031757
16.

Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retina

(Submitter supplied) Cone photoreceptors are the primary initiator of visual transduction in the human retina. Dysfunction or death of rod photoreceptors precedes cone loss in many retinal and macular degenerative diseases, suggesting a rod-dependent trophic support for cone survival. Rod differentiation and homeostasis are dependent on the basic motif leucine zipper transcription factor NRL. The loss of Nrl in mice (Nrl-/-) results in a retina with predominantly S-opsin containing cones that exhibit molecular and functional characteristics of WT cones. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6193
20 Samples
Download data: CEL
Series
Accession:
GSE33674
ID:
200033674
17.

Temporal Concordance between Apical and Transcriptional Points-of-Departure for Chemical Risk Assessment

(Submitter supplied) The number of legacy chemicals without toxicity reference values combined with the rate of new chemical development are overwhelming the capacity of the traditional risk assessment paradigm. More efficient approaches are needed to quantitatively estimate chemical risks. In this study, rats were dosed orally with multiple doses of six chemicals for 5 days, 2, 4, and 13 weeks. Target organs were analyzed for traditional histological and organ weight changes and transcriptional changes using microarrays. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL16985
720 Samples
Download data: CEL
Series
Accession:
GSE45892
ID:
200045892
18.

Temporal ChIP-on-Chip of RNA-Polymerase-II to detect novel gene activation events during photoreceptor maturation

(Submitter supplied) RNA Polymerase-II active regions were mapped comparing mouse neural retina tissue at age P25 and P2 to find novel gene activation predictions during maturation of photoreceptors. Over 800 predictions of increased activation were novel compared to previous mRNA expression array studies.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL5811
3 Samples
Download data: BED, CEL
Series
Accession:
GSE19999
ID:
200019999
19.

Transcriptome and microRNA data involved in Japanese flounder (Paralichthys olivaceus) albinism

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Paralichthys olivaceus
Type:
Non-coding RNA profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL23520
12 Samples
Download data
Series
Accession:
GSE99343
ID:
200099343
20.

microRNA data involved in Japanese flounder (Paralichthys olivaceus) albinism

(Submitter supplied) In this study, a high-throughput sequencing strategy was employed to identify the miRNAs involved in P. olivaceus albinism. High-throughput miRNA sequencing identified a total of 475 miRNAs, including 64 novel miRNAs. Furthermore, 33 differentially expressed miRNAs containing 13 up-regulated and 20 down-regulated miRNAs were identified in albino versus normally pigmented individuals (fold change ≥1.5 or ≤0.67 and p≤0.05).
Organism:
Paralichthys olivaceus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23520
6 Samples
Download data: XLS
Series
Accession:
GSE99342
ID:
200099342
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