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accession-icon GSE112681
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: a biomarker study
  • organism-icon Homo sapiens
  • sample-icon 1117 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V3.0 expression beadchip

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.

Sample Metadata Fields

Sex, Disease

View Samples
accession-icon GSE112676
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: a biomarker study [HT12_V3]
  • organism-icon Homo sapiens
  • sample-icon 741 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V3.0 expression beadchip

Description

Transcriptome-wide analysis of whole blood gene expression profiles of ALS patients, gender- and age-matched controls and patients diagnosed with diseases mimicking ALS at a tertiary referral center for motor neuron diseases.

Publication Title

Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.

Sample Metadata Fields

Sex, Disease

View Samples
accession-icon GSE112680
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: a biomarker study [HT12_V4]
  • organism-icon Homo sapiens
  • sample-icon 376 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V3.0 expression beadchip

Description

Transcriptome-wide analysis of whole blood gene expression profiles of ALS patients, gender- and age-matched controls and patients diagnosed with diseases mimicking ALS at a tertiary referral center for motor neuron diseases.

Publication Title

Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.

Sample Metadata Fields

Sex, Disease

View Samples
accession-icon GSE15914
Interleukin-7 promotes monocyte/macrophage arrest on endothelial cells
  • organism-icon Mus musculus
  • sample-icon 9 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

Background: It is recognized that atherosclerosis can regresses at least in animal models. However, little is known about the mechanisms. We induced regression of advanced atherosclerosis in apolipoprotein E deficient (APOE/) mice and studied underlying mechanisms. Unexpectedly, our study led to the role of interleukin-7 (IL-7) in atherogenesis.

Publication Title

Interleukin-7 induces recruitment of monocytes/macrophages to endothelium.

Sample Metadata Fields

Sex, Age

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accession-icon SRP045867
RNA-seq of young and quiescent MRC-5 human fibroblasts
  • organism-icon Homo sapiens
  • sample-icon 6 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2500, IlluminaHiSeq2000

Description

Quiescent MRC-5 fibroblasts were compared to young fibroblasts Jena Centre for Systems Biology of Ageing - JenAge (www.jenage.de) Overall design: 6 samples: 3 biological replicates for each age group: young and quiescent MRC-5 cells. 50bp, single-end reads, no strand-specific reads

Publication Title

Long-term quiescent fibroblast cells transit into senescence.

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP051599
RNA-seq of human fibroblasts during normal aging and during aging with rotenone perturbation
  • organism-icon Homo sapiens
  • sample-icon 60 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2500, IlluminaHiSeq2000

Description

Human fibroblasts at different population doublings were treated with low amounts of rotenone (mild stress) and compared to untreated fibroblasts. Two different cell lines were used (MRC-5, HFF). Illumina sequencing (HiSeq2000) was applied to generate 50bp single-end reads. Jena Centre for Systems Biology of Ageing - JenAge (www.jenage.de) Overall design: 60 samples: 3 biological replicates for each group: MRC-5 cells at 4 different population doublings (PD) with and without rotenone; HFF cells at 6 different population doublings with and without rotenone

Publication Title

Hormetic effect of rotenone in primary human fibroblasts.

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP069773
RNA-seq of human fibroblasts after irradiation
  • organism-icon Homo sapiens
  • sample-icon 6 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2500

Description

Comparing gene expression level by Illumina sequencing of fibroblasts after irradiation Jena Centre for Systems Biology of Ageing - JenAge (www.jenage.de) Overall design: 6 samples, 3 samples per group, 2 groups: 1) MRC-5 cells population doublings (PD) 16 and irradiation (20GY) and 2) HFF cells PD32 and irradiation (20GY)

Publication Title

Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence.

Sample Metadata Fields

No sample metadata fields

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accession-icon SRP050179
RNA-seq of human fibroblasts during replicative senescence
  • organism-icon Homo sapiens
  • sample-icon 45 Downloadable Samples
  • Technology Badge IconIlluminaHiSeq2000

Description

Senescent human fibroblasts were compared to young proliferating fibroblasts. Five different cell lines were compared. Illumina sequencing (HiSeq2000) was applied to generate 50bp single-end reads. Jena Centre for Systems Biology of Ageing - JenAge (www.jenage.de) Overall design: 48 samples: 3 biological replicates for each group: young proliferating and senescent BJ cells; young proliferating and senescent Wi-38 cells; young proliferating and senescent IMR-90 cells; 5 population doubling from young proliferating to senescent cell for HFF and MRC-5 cells

Publication Title

Conserved Senescence Associated Genes and Pathways in Primary Human Fibroblasts Detected by RNA-Seq.

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon GSE32223
Transcriptional profile of ER71 EYFP positive/negative cells in ER71 WT and MT embryos
  • organism-icon Mus musculus
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

ER71 mutant embryos are nonviable and lack hematopoietic and endothelial lineages. To further define the functional role for ER71 in cell lineage decisions, we generated genetically modified mouse models. We engineered an ER71-EYFP transgenic mouse model by fusing the 3.9 kb ER71 promoter to the EYFP reporter gene. Using FACS and transcriptional profiling, we examined the EYFP+ populations of cells in ER71 mutant and wildtype littermates. In the absence of ER71, we observed an increase in the number of EYFP expressing cells, increased expression of the cardiac molecular program and decreased expression of the hemato-endothelial program compared to the wildtype littermate controls. We have also generated a novel ER71-Cre transgenic mouse model using the same 3.9 kb ER71 promoter. Genetic fate mapping studies revealed that the ER71 expressing cells daughter hematopoietic and endothelial lineages in the wildtype background. In the absence of ER71, these cell populations contributed to alternative mesodermal lineages including the cardiac lineage. To extend these analyses, we used an inducible ES/EB system and observed that ER71 overexpression repressed cardiogenesis. Together, these studies identify ER71 as a critical regulator of mesodermal fate decisions, acting to specify the hematopoietic and endothelial lineages at the expense of cardiac lineages. This enhances our understanding of the mechanisms that govern mesodermal fate decisions early during embryogenesis.

Publication Title

ER71 directs mesodermal fate decisions during embryogenesis.

Sample Metadata Fields

Specimen part

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accession-icon GSE36555
Host-influenza A virus(infA) interactions
  • organism-icon Homo sapiens
  • sample-icon 40 Downloadable Samples
  • Technology Badge IconIllumina HumanHT-12 V3.0 expression beadchip

Description

This SuperSeries is composed of the SubSeries listed below.

Publication Title

Temporal- and strain-specific host microRNA molecular signatures associated with swine-origin H1N1 and avian-origin H7N7 influenza A virus infection.

Sample Metadata Fields

Cell line

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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)

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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