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Links from GEO DataSets

Items: 14

1.
Full record GDS5375

DEK oncogene deficiency effect in U937 leukemic monocyte lymphoma cells

Analysis of U937 cells following DEK oncogene knockdown by two different shRNAs (shDEK14, shDEK17). The DEK gene is highly expressed in many types of cancer cells and involved in chromosomal translocation in acute myelogenous leukemia. Results provide insight into the role of DEK in gene regulation.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 protocol sets
Platform:
GPL10558
Series:
GSE60732
9 Samples
Download data
2.

DNA methylation analysis of the U937 cell line

(Submitter supplied) DNA methylation profiling of gene promoters in the human myeloid cell line U937.
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL8490
2 Samples
Download data: TXT
Series
Accession:
GSE60734
ID:
200060734
3.

Gene expression changes upon knockdown of DEK in the U937 cell line

(Submitter supplied) Gene expression profiling of U937 cells upon knockdown of the DEK oncogene by two different shRNAs (shDEK14 and shDEK17).
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5375
Platform:
GPL10558
9 Samples
Download data: TXT
Series
Accession:
GSE60732
ID:
200060732
4.

Genome-wide mapping of DEK binding in the U937 cell line

(Submitter supplied) We find that the DEK oncoprotein preferentially binds close to the transcription start sites of highly and ubiquitously expressed genes.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: BED, TXT
Series
Accession:
GSE60692
ID:
200060692
5.

Identifying DEK-dependent transcriptional signatures in HPV+ and HPV- head and neck squamous cell carcinoma (HNSCC)

(Submitter supplied) We report the first RNA-Seq experiments profiling the effects of DEK loss in HNSCC. Our data also incorporates HPV+ and HPV- tumors to idenfity HPV-dependent and -independent gene signatures.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
4 Samples
Download data: TXT
6.

The Role of nuclear protein DEK in hematopoietic stem cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
22 Samples
Download data: NARROWPEAK
Series
Accession:
GSE166434
ID:
200166434
7.

Genome-wide Maps of Chromatin State in Control and DEK-deficient Hematopoietic Stem Cells [CUT&Tag]

(Submitter supplied) Purpose:To identify chromatin state involved in the DEK regulating gene expression of hematopoietic stem cells (HSC) in mice, we performed DEK, H3K27ac, H3K4me3 and H3K9ac CUT&Tag in HSC or LSK cells freshly sorted from mice.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
9 Samples
Download data: NARROWPEAK
Series
Accession:
GSE166433
ID:
200166433
8.

ATAC Sequencing Facilitates the Role of Nuclear Protein DEK in Regulating Chromatin Accessibility of Hematopoietic Stem Cells [ATAC-seq]

(Submitter supplied) Purpose:To identify genes involved in the DEK regulating chromatin accessibility of hematopoietic stem cells (HSC) in mice, we performed ATAC-Sequence of HSC freshly sorted from mice.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: NARROWPEAK
Series
Accession:
GSE166432
ID:
200166432
9.

Next Generation Sequencing Facilitates Quantitative Analysis of the Role of nuclear protein DEK in hematopoietic stem cells [RNA-seq]

(Submitter supplied) Purpose:To identify genes and the molecular pathways involved in the DEK regulating hematopoietic stem cells (HSC) in mice, we performed RNA-Sequence of HSC freshly sorted from mice. Methods: mRNA profiles of HSC in Dekfl/fl (floxp) and Dekfl/fl,Tie2-Cre (cKO) were generated by deep sequencing, in triplicate, using Illumina HiSeq 2000. Results:Using an optimized data analysis workflow, we mapped about 50 million sequence reads per sample to the mouse genome (build mm10) and identified 33299 transcripts in HSC (the floxp and cKO group) with BWA workflow. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
7 Samples
Download data: XLS
Series
Accession:
GSE166431
ID:
200166431
10.

Expression data from MDA-MB-231 cells over-expressing RRP1B and MDA-MB-231 control cells with endogenous RRP1B levels

(Submitter supplied) RRP1B is a breast cancer metastasis suppressor that interacts with various regulators of gene transcription We examined the changes in gene expression caused by the stable over-expression of RRP1B using lentiviral transduction in the human breast cancer cell line MDA-MB-231.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
10 Samples
Download data: CEL
Series
Accession:
GSE53979
ID:
200053979
11.

Expression data from pediatric AML patients

(Submitter supplied) Pediatric acute myeloid leukemia (AML) is a heterogeneous disease characterized by non-random genetic aberrations related to outcome. Detecting these aberrations however still lead to failures or false negative results. Therefore, we focused on the potential of gene expression profiles (GEP) to classify pediatric AML. Gene expression microarray data of 237 children with AML were generated and cases were split into a discovery cohort (n=157) and an independent validation cohort (n=80). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
237 Samples
Download data: CEL
Series
Accession:
GSE17855
ID:
200017855
12.

Expression data from NFI-C knock out embryonic fibroblasts

(Submitter supplied) The Nuclear Factor I C (NFI-C) transcription factor has been implicated in TGF-β signaling, extracellular matrix deposition and skin appendage pathologies. We performed a global gene expression analysis in NFI-C-/- and wild-type embryonic primary murine fibroblasts. This indicated that NFI-C acts mostly to repress gene expression in response to TGF-β1. Misregulated genes featured a prominent over-representation of regulators of connective tissue inflammation and repair.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
18 Samples
Download data: CEL
Series
Accession:
GSE15871
ID:
200015871
13.

Genome-wide mapping of Nuclear Factor I binding sites using ChIP-Seq in WT and NFI-C knock-out MEFs

(Submitter supplied) The Nuclear Factor I (NFI) family of DNA binding proteins (also called CAAT box transcription factors or CTF) is involved both in replication of adenoviral DNA and in regulation of gene expression. Using chromatin immuno-precipitation and high throughput sequencing (method termed ChIP-Seq) we performed genome-wide mapping of Nuclear Factor I DNA binding sites in mouse embryonic fibroblasts. We found that in vivo and in vitro NFI binding specificities are identical, since previously established position weight matrix was found to accurately predict binding sites for NFI group of proteins. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
3 Samples
Download data: BED, SGA, TXT, WIG
Series
Accession:
GSE15844
ID:
200015844
14.

Differential ChIP-Seq of RNAPol2 and H3K4me3 during a parabolic flight

(Submitter supplied) Primary human macrophages in in vitro conditions have been exposed to hypergravity and microgravity during the 28th DLR parabolic flight campaign
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: BED
Series
Accession:
GSE221397
ID:
200221397
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