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accession-icon GSE33478
Genome-wide DNA methylation and gene expression analyses of monozygotic twin discordant for intelligence levels
  • organism-icon Homo sapiens
  • sample-icon 27 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Promoter 1.0R Array (hsprompr), Affymetrix Human Gene 1.0 ST Array (hugene10st)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Genome-wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels.

Sample Metadata Fields

Specimen part

View Samples
accession-icon GSE33476
Expression data from phenotypically discordant monozygotic twin lymphoblasts
  • organism-icon Homo sapiens
  • sample-icon 27 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.0 ST Array (hugene10st), Affymetrix Human Promoter 1.0R Array (hsprompr)

Description

Human intelligence demonstrates one of the highest heritabilities among human quantitative traits. Phenotypically discordant monozygotic twins provide a way to identify loci responsible for normal-range intelligence.

Publication Title

Genome-wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels.

Sample Metadata Fields

Specimen part

View Samples
accession-icon GSE42808
Expression data from human umbilical vein endothelial cells (HUVEC) treated with DMSO, telmisartan, or telmisartan and amlodipine
  • organism-icon Homo sapiens
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.0 ST Array (hugene10st)

Description

Objective Telmisartan, an angiotensin II type 1 (AT1) receptor blocker, and amlodipine, a calcium channel blocker, are antihypertensive agents clinically used as monotherapy or in combination. They exert beneficial cardiovascular effects independently of blood pressure lowering and classic mechanisms of action. In this study, we investigate molecular mechanisms responsible for the off-target effects of telmisartan and telmisartan-amlodipine in endothelial cells (EC), using an unbiased approach.

Publication Title

Telmisartan exerts pleiotropic effects in endothelial cells and promotes endothelial cell quiescence and survival.

Sample Metadata Fields

Specimen part, Disease, Treatment

View Samples
accession-icon GSE45564
Expression data in the presence of miR-29a inhibition in human dermal fibroblast cells
  • organism-icon Homo sapiens
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Gene 1.0 ST Array (hugene10st)

Description

miR-29 can target many gene transcripts encoding extracellular matrix proteins. To unravel novel targets, we used microarray analysis to detect global gene expression changes when inhibiting endogenous miR-29.

Publication Title

Ten-eleven translocation (Tet) and thymine DNA glycosylase (TDG), components of the demethylation pathway, are direct targets of miRNA-29a.

Sample Metadata Fields

Specimen part, Treatment

View Samples
accession-icon GSE11103
Study of human immune and memory T cells using microarray
  • organism-icon Homo sapiens
  • sample-icon 39 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Deconvolution of blood microarray data identifies cellular activation patterns in systemic lupus erythematosus.

Sample Metadata Fields

Specimen part, Disease

View Samples
accession-icon GSE11057
Memory T Cell Subsets
  • organism-icon Homo sapiens
  • sample-icon 16 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Microarray deconvolution is a technique for quantifying the relative abundance of constituent cells in a mixture based on that mixture's microarray signature and the signatures of the purified constituents. It has been applied to yeast and other systems but not to blood samples.

Publication Title

Deconvolution of blood microarray data identifies cellular activation patterns in systemic lupus erythematosus.

Sample Metadata Fields

Specimen part, Disease

View Samples
accession-icon GSE11058
Immune Cell Line Mixtures
  • organism-icon Homo sapiens
  • sample-icon 16 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Microarray deconvolution is a technique for quantifying the relative abundance of constituent cells in a mixture based on that mixture's microarray signature and the signatures of the purified constituents. Its ability to discriminate related human cells is unknown.

Publication Title

Deconvolution of blood microarray data identifies cellular activation patterns in systemic lupus erythematosus.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon SRP099018
Single cell RNA expression of mouse embryonic basal forebrain
  • organism-icon Mus musculus
  • sample-icon 225 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Single-cell RNA-Seq RNA from medial ganglionic eminence at E11.5, E13.5, E15.5 or E17.5. The ID of this project in Genentech''s ExpressionPlot database is PRJ0007389 Overall design: Single-cell RNA-Seq from medial ganglionic eminence at E11.5, E13.5, E15.5 or E17.5.

Publication Title

Single-cell RNA sequencing identifies distinct mouse medial ganglionic eminence cell types.

Sample Metadata Fields

Specimen part, Subject

View Samples
accession-icon SRP098938
Embryonic stem cells-derived neural progenitor cells
  • organism-icon Mus musculus
  • sample-icon 140 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

J14 ES cells differentiated into MGE-like cells. Three groups of single-cell preparations were analyzed: ES cells (undifferentiated), differentiated cells (unsorted, of which less than 10% are GFP+) and GFP+ differentiated cells. These are specified in the "group" sample characteristic, with values "ES", "Unsorted" and "GFP+" respectively. The "SAMPLE_ID" sample characteristic is a sample identifier internal to Genentech. The ID of this project in Genentech''s ExpressionPlot database is PRJ0007904 Overall design: J14 ES cells differentiated into MGE-like cells

Publication Title

Single-cell RNA sequencing identifies distinct mouse medial ganglionic eminence cell types.

Sample Metadata Fields

Cell line, Subject

View Samples
accession-icon GSE30956
Expression data from pig BMDM treated with salmonella LPS
  • organism-icon Sus scrofa
  • sample-icon 22 Downloadable Samples
  • Technology Badge Icon Affymetrix Porcine Genome Array (porcine)

Description

Mouse bone marrow-derived macrophages (BMDM) grown in macrophage colony-stimulating factor (CSF-1) have been used widely in studies of macrophage biology and the response to toll-like receptor agonists. We investigated whether similar cells could be derived from the domestic pig. Cultivation of pig bone marrow cells for 5-7 days in presence of rhCSF-1 generated a pure population of BMDM that expressed the usual macrophage markers (CD14, CD16, CD163, CD172a), are potent phagocytic cells and produced tumor necrosis factor (TNF) in response to lipopolysaccharide (LPS). Bone marrow cells could be stored frozen and thawed, providing a renewable resource.

Publication Title

Pig bone marrow-derived macrophages resemble human macrophages in their response to bacterial lipopolysaccharide.

Sample Metadata Fields

Sex, Specimen part, Time

View Samples
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refine.bio is a repository of uniformly processed and normalized, ready-to-use transcriptome data from publicly available sources. refine.bio is a project of the Childhood Cancer Data Lab (CCDL)

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Cite refine.bio

Casey S. Greene, Dongbo Hu, Richard W. W. Jones, Stephanie Liu, David S. Mejia, Rob Patro, Stephen R. Piccolo, Ariel Rodriguez Romero, Hirak Sarkar, Candace L. Savonen, Jaclyn N. Taroni, William E. Vauclain, Deepashree Venkatesh Prasad, Kurt G. Wheeler. refine.bio: a resource of uniformly processed publicly available gene expression datasets.
URL: https://www.refine.bio

Note that the contributor list is in alphabetical order as we prepare a manuscript for submission.

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