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accession-icon GSE30112
Transcript profiling of soybean msh1 RNAi transgenic lines
  • organism-icon Glycine max
  • sample-icon 10 Downloadable Samples
  • Technology Badge Icon Affymetrix Soybean Genome Array (soybean)

Description

The soybean msh1 RNAi transgenic line show various growth phenotype. We use microarray analysis to characterize gene expression pattern for two of the phenotypes - variegation and stunted growth.

Publication Title

MutS HOMOLOG1 is a nucleoid protein that alters mitochondrial and plastid properties and plant response to high light.

Alternate Accession IDs

E-GEOD-30112

Sample Metadata Fields

Specimen part

View Samples
accession-icon GSE30281
Transcript profiling of Arabidopsis albino msh1 mutants
  • organism-icon Arabidopsis thaliana
  • sample-icon 6 Downloadable Samples
  • Technology Badge Icon Affymetrix Arabidopsis ATH1 Genome Array (ath1121501)

Description

The soybean msh1 RNAi transgenic line show various growth phenotype. We use microarray analysis to characterize gene expression pattern for two of the phenotypes - variegation and stunted growth.

Publication Title

MutS HOMOLOG1 is a nucleoid protein that alters mitochondrial and plastid properties and plant response to high light.

Alternate Accession IDs

E-GEOD-30281

Sample Metadata Fields

Specimen part

View Samples
accession-icon SRP144221
Gene expression in cultured mouse neural progenitor cells
  • organism-icon Mus musculus
  • sample-icon 24 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

Bulk RNA sequencing data from neural progenitor cells under conditions of low or high growth factor and Notch pathway activation Overall design: Cells were treated with high (20 ng/ml EGF and FGF) or low (0.5 ng/ml EGF) recombinant growth factors, with or without Notch pathway inhibitor (DAPT, 10 uM) for 12h.

Publication Title

<i>Cis-</i>activation in the Notch signaling pathway.

Alternate Accession IDs

GSE113937

Sample Metadata Fields

Specimen part, Subject

View Samples
accession-icon SRP062011
Combinatorial gene regulation by modulation of relative pulse timing
  • organism-icon Saccharomyces cerevisiae
  • sample-icon 27 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

We performed RNAseq with Saccharomyces cerevisiae cells under both transient and steady-state conditions to study the regulation of genes by two pulsatile transcription factors, Msn2 and Mig1. The transient data allowed us to identify combinatorial targets while the steady-state data was used to study target expression dependence on the relative pulse timing between the two TFs. Overall design: For transition experiments, 18 samples (3 different strains x 3 dfferent conditions x 2 biological replicates) were analyzed. For steady-state experiments, one strain was analyzed at 9 different glucose concentrations and the other strain was analyzed at one glucose condition.

Publication Title

Combinatorial gene regulation by modulation of relative pulse timing.

Alternate Accession IDs

GSE71712

Sample Metadata Fields

Cell line, Subject

View Samples
accession-icon SRP084395
RNA-seq of mouse embryonic stem cell states expressing Esrrb, Tbx3, and Zscan4
  • organism-icon Mus musculus
  • sample-icon 10 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

We develop a theoretical-computational framework for inferring cell state transition dynamics, and apply it to mouse embryonic stem cells states defined by expression levels of Esrrb, Tbx3, and Zscan4. RNA-seq was performed to characterize the larger transcriptional differences between states expressing combinations of these three specific genes, and proceed to explore their dynamic interconversion. Overall design: A double knock-in reporter for Esrrb and Tbx3 with distinct fluorescent proteins was constructed to enable purification of substates defined by their relative expression levels (Esrrb-/Tbx3-; Esrrb+/Tbx3-; Esrrb+/Tbx3+). A second line was constructed using a promoter-fragment reporter to isolate Zscan4+ from Zscan4- cells. Following FACS isolation, the subpopulations were sequenced on an Illumina HiSeq2500. Biological replicates were collected on different days.

Publication Title

Inferring Cell-State Transition Dynamics from Lineage Trees and Endpoint Single-Cell Measurements.

Alternate Accession IDs

GSE86417

Sample Metadata Fields

Specimen part, Subject

View Samples
accession-icon SRP063515
Response of C2C12-hN1?ECD to DAPT washout
  • organism-icon Mus musculus
  • sample-icon 6 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

C2C12 cells expressing constitutively active hN1?ECD were activated by complete DAPT washout for 1h or 6h, or left in 10 uM DAPT Overall design: 2 Samples and 1 Control

Publication Title

Dynamic Ligand Discrimination in the Notch Signaling Pathway.

Alternate Accession IDs

GSE72847

Sample Metadata Fields

Specimen part, Subject

View Samples
accession-icon SRP106658
Combinatorial Signal Preception in the BMP Pathway
  • organism-icon Mus musculus
  • sample-icon 22 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500

Description

These data consist of an expression survey of three receptor cell lines and the parental cell types was performed to determine expression of BMP related genes. Overall design: Sequence libraries for three cell types were constructed using NEBNext Ultra RNA-seq (NEB #E7530) and sequenced on Illumnia HiSeq2500.

Publication Title

Combinatorial Signal Perception in the BMP Pathway.

Alternate Accession IDs

GSE98674

Sample Metadata Fields

Cell line, Subject

View Samples
accession-icon SRP038871
Noncoding RNA transcriptome analysis during cellular reprogramming
  • organism-icon Mus musculus
  • sample-icon 119 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2500, Illumina HiSeq 2000

Description

We report the application of single-cell and bulk RNA sequencing technology to examine the noncoding transcriptome of cells undergoing reprogramming to the pluripotent state. Overall design: Examination of noncoding RNAs in reprogrammming cells. We examined iPS cells grown in standard ES cell culture conditions, as well as iPS cells grown in "2i" conditions (small molecule inhibition of Mek and Gsk3). We also compared our iPS samples to male and female ES cells (mES, fES).

Publication Title

Single-cell transcriptome analysis reveals dynamic changes in lncRNA expression during reprogramming.

Alternate Accession IDs

GSE55291

Sample Metadata Fields

No sample metadata fields

View Samples
accession-icon SRP068162
Asynchronous combinatorial action of four regulatory factors activates Bcl11b for T cell commitment
  • organism-icon Mus musculus
  • sample-icon 90 Downloadable Samples
  • Technology Badge IconIllumina HiSeq 2000

Description

During T cell development, multipotent progenitors relinquish competence for other fates and commit to the T cell lineage by turning on Bcl11b, which encodes a transcription factor. To clarify lineage commitment mechanisms, we followed developing T cells at the single-cell level using Bcl11b knock-in fluorescent reporter mice. Notch signaling and Notch activated transcription factors collaborate to activate Bcl11b expression irrespectively of Notch-dependent proliferation. These inputs work via three distinct, asynchronous mechanisms: an early locus ‘poising’ function dependent on TCF-1 and GATA-3, a stochastic-permissivity function dependent on Notch signaling, and a separate amplitude-control function dependent on Runx1, a factor already present in multipotent progenitors. Despite their necessity for Bcl11b activation, these inputs act in a stage specific manner, providing a multitiered mechanism for developmental gene regulation. Overall design: Two sets of samples were generated from DN T-cell sub-populations derived from culture of bone marrow progenitors from mice containing a knock-in Bcl11b-YFP reporter

Publication Title

Asynchronous combinatorial action of four regulatory factors activates Bcl11b for T cell commitment.

Alternate Accession IDs

GSE76606

Sample Metadata Fields

Specimen part, Subject

View Samples
accession-icon GSE10392
Gene regulation profile of Medroxyprogesterone acetate (MPA)-treated late pregnant cervix
  • organism-icon Mus musculus
  • sample-icon 12 Downloadable Samples
  • Technology Badge Icon Affymetrix Mouse Genome 430 2.0 Array (mouse4302)

Description

Noval and traditional signaling pathways involved in cervical ripening that were regulated by MPA were identified.

Publication Title

Preventing cervical ripening: the primary mechanism by which progestational agents prevent preterm birth?

Alternate Accession IDs

E-GEOD-10392

Sample Metadata Fields

No sample metadata fields

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)

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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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