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accession-icon SRP023548
Homo sapiens strain:U-251 MG Transcriptome or Gene expression
  • organism-icon Homo sapiens
  • sample-icon 16 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

Degraded RNA - RNA with low RIN. U-251 MG brain gliablastoma cell line.

Publication Title

No associated publication

Sample Metadata Fields

Specimen part

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accession-icon SRP043027
Homo sapiens strain:U2OS Transcriptome or Gene expression
  • organism-icon Homo sapiens
  • sample-icon 15 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2000

Description

To adapt a non-strandaed library preparation protocol into a strand specific one in an automated fashion. Use the data to emphasize the advantages of strand specific data.

Publication Title

No associated publication

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP043688
Homo sapiens strain:Cell line Transcriptome or Gene expression
  • organism-icon Homo sapiens
  • sample-icon 9 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2500

Description

The study goal was to develop a new and robust protocol for blood preservation. It also involved a proof-of-concept study to preserve rare cell samples.

Publication Title

No associated publication

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP019968
Homo sapiens Transcriptome or Gene expression
  • organism-icon Homo sapiens
  • sample-icon 8 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

RNA sequencing data for four cell lines representing different stages during malignant transformation.

Publication Title

Majority of differentially expressed genes are down-regulated during malignant transformation in a four-stage model.

Sample Metadata Fields

No sample metadata fields

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accession-icon GSE76172
Treatment of bone marrow-derived macrophages with hFc-FNDC4 recombinant protein
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Gene 1.1 ST Array (mogene11st)

Description

FNDC4 is a novel secreted factor sharing high homology with the exercise-associated myokine irisin (FNDC5). Here we report that Fndc4 is robustly upregulated in various mouse models of inflammation as well as in human inflammatory conditions. Specifically, subjects with inflammatory bowel disease show increased FNDC4 levels locally at inflamed sites of the intestine. Interestingly, administration of recombinant FNDC4 during colitis development in mice resulted in markedly reduced disease severity compared to mice injected with a control protein. Conversely, mice that lacked Fndc4 showed increased colitis severity. Analysis of binding of FNDC4 to different immune cell types revealed strong and specific binding to macrophages and monocytes. FNDC4 treatment of bone marrow-derived macrophages in vitro resulted in reduced phagocytosis, improved survival and reduced pro-inflammatory chemokine expression. Hence, treatment with FNDC4 resulted in a state of dampened macrophage activity, while enhancing their survival. Thus, we have characterized a novel factor with direct therapeutic potential in inflammatory bowel disease and possibly other inflammatory diseases.

Publication Title

FNDC4 acts as an anti-inflammatory factor on macrophages and improves colitis in mice.

Sample Metadata Fields

Sex, Specimen part, Treatment

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accession-icon SRP099312
RNAseq of Adipose tissues in VEGF and VEGFB knockout mouse models
  • organism-icon Mus musculus
  • sample-icon 10 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

VEGF and VEGFB Play Balancing Roles in Adipose Differentiation, Gene Expression and Function

Publication Title

No associated publication

Sample Metadata Fields

Sex, Specimen part, Cell line

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accession-icon SRP194050
mouse brain and lung Transcriptome
  • organism-icon Mus musculus
  • sample-icon 4 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

gene expression study on brain and lung under Dip2a regulation to better understand the role of Dip2a gene during mice brain and lung development.

Publication Title

Large genomic fragment deletions and insertions in mouse using CRISPR/Cas9.

Sample Metadata Fields

Sex, Specimen part, Cell line

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accession-icon E-MEXP-402
Transcription profiling of wild type mice stomach and colon samples
  • organism-icon Mus musculus
  • sample-icon 2 Downloadable Samples
  • Technology Badge Icon Affymetrix Murine Genome U74A Version 2 Array (mgu74av2)

Description

Comparison of stomach and colon in normal mice.

Publication Title

No associated publication

Sample Metadata Fields

Sex, Age, Specimen part

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accession-icon GSE66937
The transcriptomes of suicide completers and deceased controls.
  • organism-icon Homo sapiens
  • sample-icon 66 Downloadable Samples
  • Technology Badge Icon Affymetrix Human Transcriptome Array 2.0 (hta20)

Description

Neurobiological causes of suicide are largely unknown. Volumes and dysfunction of brain regions amygdala, hippocampus, prefrontal cortex and thalamus were reported to play a role in suicidal intention.

Publication Title

No associated publication

Sample Metadata Fields

Subject

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accession-icon GSE66738
Effect of cathepsin inhibitors in signals associated with Th1 and Th2 mediators by Dendritic Cells
  • organism-icon Mus musculus
  • sample-icon 14 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

Cathepsin inhibitors have been associated to induce changes in Th1/Th2 polarization; cathepsin B inhibitor CA074 has been reported to induce a Th1 polarization, whereas cathepsin L inhibitor CLIK148 has been reported to induce a Th2 polarization.

Publication Title

No associated publication

Sample Metadata Fields

Specimen part, Treatment

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

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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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