refine.bio
  • Search
      • Normalized Compendia
      • RNA-seq Sample Compendia
  • Docs
  • About
  • My Dataset
github link
Showing
of 134 results
Sort by

Filters

Technology

Platform

accession-icon GSE31341
The Phytoestrogen Genistein Is a Tissue-Specific Androgen Receptor Modulator
  • organism-icon Mus musculus
  • sample-icon 21 Downloadable Samples
  • Technology Badge IconIllumina MouseWG-6 v2.0 expression beadchip

Description

We report that the phytoestrogen genistein acts as a tissue-specific androgen receptor modulator in mouse using a novel androgen reporter mouse line and gene expression profiling. Genistein is a partial androgen agonist/antagonist in prostate, brain, and testis but not in skeletal muscle or lung. Gene expression profiling has been done from prostates of intact and castrated male mice treated with genistein or vehicle. Gene expression profiling was also done from prostates of estradiol-treated intact male mice.

Publication Title

The phytoestrogen genistein is a tissue-specific androgen receptor modulator.

Sample Metadata Fields

Sex, Specimen part

View Samples
accession-icon GSE20752
Comparative Epigenomic Analysis of Murine and Human Adipogenesis
  • organism-icon Mus musculus, Homo sapiens
  • sample-icon 26 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

Comparative epigenomic analysis of murine and human adipogenesis.

Sample Metadata Fields

Sex, Specimen part

View Samples
accession-icon GSE20697
Expression profiling of human adipose stromal cell (hASC) adipogenesis
  • organism-icon Homo sapiens
  • sample-icon 18 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Human abdominal adipose tissue was obtained with informed consent from a 33-year old Caucasian female (BMI = 32.96 Kg/m2) undergoing lipoaspiration. Adipose stromal cells (hASCs) were isolated and differentiated into adipocytes in vitro.

Publication Title

Comparative epigenomic analysis of murine and human adipogenesis.

Sample Metadata Fields

Sex, Specimen part

View Samples
accession-icon GSE12207
Biofilms and type III secretion are not mutually exclusive in Pseudomonas aeruginosa
  • organism-icon Pseudomonas aeruginosa
  • sample-icon 15 Downloadable Samples
  • Technology Badge Icon Affymetrix Pseudomonas aeruginosa Array (paeg1a)

Description

Biofilm formation and type III secretion have been shown to be reciprocally regulated in P. aeruginosa, and it has been suggested that factors related to acute infection may be incompatible

Publication Title

Biofilms and type III secretion are not mutually exclusive in Pseudomonas aeruginosa.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE58193
Characterizing the profiles of Ebf1 in mouse fat cells.
  • organism-icon Mus musculus
  • sample-icon 9 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

gene expression data from mouse adipocyte, with and without Ebf1 knock-down

Publication Title

Early B-cell factor-1 (EBF1) is a key regulator of metabolic and inflammatory signaling pathways in mature adipocytes.

Sample Metadata Fields

Specimen part

View Samples
accession-icon GSE20696
Expression profiling of 3T3-L1 adipogenesis
  • organism-icon Mus musculus
  • sample-icon 8 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

3T3-L1 pre-adipocyte cells were grown to confluence and induced to differentiate in adipogeneic media.

Publication Title

Comparative epigenomic analysis of murine and human adipogenesis.

Sample Metadata Fields

Specimen part

View Samples
accession-icon SRP072289
Dynamics of lineage commitment revealed by single-cell transcriptomics of differentiating embryonic stem cells
  • organism-icon Mus musculus
  • sample-icon 38 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

Gene expression heterogeneity in the pluripotent state of mouse embryonic stem cells (mESCs) has been increasingly well-characterized. In contrast, exit from pluripotency and lineage commitment have not been studied systematically at the single-cell level. Here we measured the gene expression dynamics of retinoic acid driven mESC differentiation using an unbiased single-cell transcriptomics approach. We found that the exit from pluripotency marks the start of a lineage bifurcation as well as a transient phase of susceptibility to lineage specifying signals. Our study revealed several transcriptional signatures of this phase, including a sharp increase of gene expression variability and a handover between two classes of transcription factors. In summary, we provide a comprehensive analysis of lineage commitment at the single cell level, a potential stepping stone to improved lineage control through timing of differentiation cues. Overall design: Bulk and single-cell RNA-seq (SCRB-seq and SMART-seq) of mouse embryonic stem cells after different periods of continuous exposure to retinoic acid. Bulk RNA-seq of cell lines derived after retinoic exposure and after differentiation with retinoic acid and MEK inhibitor combined.

Publication Title

Dynamics of lineage commitment revealed by single-cell transcriptomics of differentiating embryonic stem cells.

Sample Metadata Fields

Cell line, Subject

View Samples
accession-icon GSE35685
Lymphoid Priming in Human Bone Marrow Begins Prior to CD10 Expression with Up-Regulation of L-selectin
  • organism-icon Homo sapiens
  • sample-icon 9 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Genome U133 Plus 2.0 Array (hgu133plus2)

Description

Studies of adult human hematopoiesis have until now relied on the expression of CD10 to define lymphoid commitment. We report a novel lymphoid-primed population in human bone marrow that is generated from hematopoietic stem cells (HSC) prior to the onset of CD10 expression and B cell commitment, and is identified by high levels of the homing molecule L-selectin (CD62L). CD10-CD62Lhi progenitors have full lymphoid (B/T/NK) potential, and show reduced myeloid and absent erythroid potential. Genome-wide gene expression analysis demonstrates that the CD10-CD62Lhi population represents an intermediate stage of differentiation between CD34+CD38- HSC and CD34+lin-CD10+ progenitors marked by down-regulation of TAL1 and MPL, upregulation of E2A, CD3E and IL2RG expression, and absent B cell commitment or RAG1/2 expression. Immature CD34+CD1a- thymocytes are also CD62Lhi and L-selectin ligands are expressed at the cortico-medullary junction, suggesting a possible role for L-selectin in human thymic homing. These studies identify the earliest stage of lymphoid priming in human bone marrow.

Publication Title

Lymphoid priming in human bone marrow begins before expression of CD10 with upregulation of L-selectin.

Sample Metadata Fields

Specimen part

View Samples
accession-icon SRP066440
Simultaneous pathway activity inference and global gene expression analysis using RNA-sequencing [myd88]
  • organism-icon Mus musculus
  • sample-icon 383 Downloadable Samples
  • Technology Badge IconNextSeq 500

Description

Two 96-well plates per genotype wild type and Myd88 knockout, 4 hour time series in 0.5 hr increments Overall design: Myd88 BMDM transcriptional profiling to complement TF-seq data

Publication Title

Simultaneous Pathway Activity Inference and Gene Expression Analysis Using RNA Sequencing.

Sample Metadata Fields

Sex, Age, Specimen part, Cell line, Treatment, Subject, Time

View Samples
accession-icon SRP066443
Simultaneous pathway activity inference and global gene expression analysis using RNA-sequencing [halofuginone]
  • organism-icon Mus musculus
  • sample-icon 120 Downloadable Samples
  • Technology Badge IconNextSeq 500

Description

Bone marrow derived macrophages treated with small molecules and stimulated with LPS Overall design: Wild-type BMDMs pretreated with small molecules for 30 minutes prior to stimulation with LPS

Publication Title

Simultaneous Pathway Activity Inference and Gene Expression Analysis Using RNA Sequencing.

Sample Metadata Fields

Sex, Age, Specimen part, Cell line, Treatment, Subject, Time

View Samples
...

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)

fund-icon Fund the CCDL

Developed by the Childhood Cancer Data Lab

Powered by Alex's Lemonade Stand Foundation

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.

BSD 3-Clause LicensePrivacyTerms of UseContact