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Links from GEO DataSets

Items: 20

1.

Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease

(Submitter supplied) Background: Genome wide association studies (GWASs) have revealed many susceptibility loci for complex genetic diseases. For most loci the causal genes have not been identified. The identification of candidate genes is currently mainly based genes that localize close to or within the identified loci. We have recently shown that 92 of the 163 Inflammatory Bowel Disease (IBD)-loci co-localize with noncoding DNA regulatory elements (DRE). more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL16791
372 Samples
Download data: WIG
Series
Accession:
GSE89441
ID:
200089441
2.

Inflammatory bowel disease risk loci overlap with DNA regulatory regions in immune cells and intestinal epithelium

(Submitter supplied) Background & Aims: The contribution of genetics to the pathogenesis of inflammatory bowel disease (IBD) has been established by twin studies, targeted sequencing and genome-wide association studies (GWASs). This has yielded a plethora of risk loci with an aim to identify causal variants. Research on the genetic components of IBD has mainly focused on protein coding genes, thereby omitting other functional elements in the human genome i.e. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16558
8 Samples
Download data: COD, TXT
Series
Accession:
GSE51425
ID:
200051425
3.

Integrative analysis of liver-specific noncoding regulatory variants associated with the risk of coronary artery disease

(Submitter supplied) We performed promoter Capture Hi-C in HepG2 to investigate interactions between gene promoters and distal elements as a transcription-regulating mechanism contributing to these phenotypes. We also performed ChIP-Seq at 2h, 8h and 23h timepoints in HepG2 for Il1B treatment.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL20301 GPL11154
10 Samples
Download data: BIGWIG, TXT
Series
Accession:
GSE157306
ID:
200157306
4.

Genome-wide chromosomal conformation elucidates regulatory relationships in human brain development and disease

(Submitter supplied) The demonstration that chromatin exhibits a complex 3 dimensional organization, whereby short and long distance physical interactions correspond to complex gene regulatory processes has opened a new window on understanding the functional organization of the human genome. Recently, chromatin remodeling has also been causally implicated in several neurodevelopmental disorders, including autism and schizophrenia. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
6 Samples
Download data: BED, HDF5
Series
Accession:
GSE77565
ID:
200077565
5.

Identification of Breast Cancer Associated Variants That Modulate Transcription Factor Binding

(Submitter supplied) GWAS have discovered thousands of genomic loci that are associated with disease risk and quantitative traits, but most of the variants responsible for risk remain uncharacterized. The vast majority of GWAS-identified loci contain non-coding SNPs and defining molecular mechanism of risk is challenging. Many non-coding causal SNPs are hypothesized to alter Transcription Factor (TF) binding sites as the mechanism by which they affect organismal phenotypes. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL18573
5 Samples
Download data: BED, BEDGRAPH, BIGWIG
Series
Accession:
GSE89013
ID:
200089013
6.

FAIRE-seq in primary human megakaryocytes, erythroblasts and monocytes

(Submitter supplied) Maps of open chromatin in three primary human blood cell types of the myeloid lineage (megakaryocytes, erythroblasts and monocytes) using the formaldehyde-assisted isolation of regulatory elements method followed by next-generation sequencing (FAIRE-seq). We also generated FAIRE-seq data in the megakaryocytic cell line CHRF-288-11. In addition to our data sets, we retrieved FAIRE-seq data for the erythroblastoid cell line K562 (ENCODE Project Consortium 2012) and pancreatic islets (Gaulton et al. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11154 GPL10999 GPL9115
6 Samples
Download data: BED
Series
Accession:
GSE37916
ID:
200037916
7.

H3K27ac profiling in control and DSS-treated colonic epithelium

(Submitter supplied) We determined changes in enhancer chromatin that occur during colonic inflammation, found that dynamic chromatin regions are enriched for HNF4A binding motirfs, and then measured HNF4A binidng by ChIP-seq in each condition.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT, WIG
Series
Accession:
GSE52426
ID:
200052426
8.

Systematic Evaluation Of Genes And Genetic Variants Associated With Type 1 Diabetes Susceptibility

(Submitter supplied) Application of Systems Genetics analysis for systematic evaluation of candidate causal genes associated with risk of Type 1 Diabetes along with follow-up bioinformatics pathway analysis.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
590 Samples
Download data: TXT
Series
Accession:
GSE77350
ID:
200077350
9.

Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci

(Submitter supplied) Genome wide association studies (GWAS) have identified single nucleotide polymorphisms (SNPs) associated with diseases of the colon including inflammatory bowel diseases (IBD) and colorectal cancer (CRC). However, the functional role of many of these SNPs is largely unknown and tissue-specific resources are lacking. Expression quantitative trait loci (eQTL) mapping identifies target genes of disease-associated SNPs. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
40 Samples
Download data: TXT
Series
Accession:
GSE56789
ID:
200056789
10.

Profiling of Ileal Transcriptome in Pediatric Crohn Disease

(Submitter supplied) We report ileal gene expression at diagnosis in a cohort of 210 treatment-naïve patients of pediatric Crohn's disease and 35 non-IBD controls from the RISK study. After three years of follow-up after diagnosis, 27 of the CD patients progressed to complicated disease (B2 and/or B3). We aim to test whether Transcriptional Risk Scores helps to distinguish between patient subgroups, improving the predictive power gained from Genetic Risk Scores.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
245 Samples
Download data: TXT
11.

Functional screen of Inflammatory bowel disease genes reveals key epithelial functions: Illumina Whole Genome Dataset

(Submitter supplied) Background: Genetic studies have been tremendously successful in identifying genomic regions associated with a wide variety of phenotypes, although the success of these studies in identifying causal genes, their variants, and their functional impacts have been more limited.   Methods: We identified 145 genes from IBD-associated genomic loci having endogenous expression within the intestinal epithelial cell compartment.  We evaluated the impact of lentiviral transfer of the open reading frame (ORF) of these IBD genes into the HT-29 intestinal epithelial cell line via transcriptomic analyses.  Comparing the genes whose expression was modulated by each ORF, as well as the functions enriched within these gene lists, identified ORFs with shared impacts and their putative disease-relevant biological functions. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
376 Samples
Download data: TXT
Series
Accession:
GSE186110
ID:
200186110
12.

Functional screen of Inflammatory bowel disease genes reveals key epithelial functions: Agilent Targeted Dataset

(Submitter supplied) Background: Genetic studies have been tremendously successful in identifying genomic regions associated with a wide variety of phenotypes, although the success of these studies in identifying causal genes, their variants, and their functional impacts have been more limited.   Methods: We identified 145 genes from IBD-associated genomic loci having endogenous expression within the intestinal epithelial cell compartment.  We evaluated the impact of lentiviral transfer of the open reading frame (ORF) of these IBD genes into the HT-29 intestinal epithelial cell line via transcriptomic analyses.  Comparing the genes whose expression was modulated by each ORF, as well as the functions enriched within these gene lists, identified ORFs with shared impacts and their putative disease-relevant biological functions. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL30867
426 Samples
Download data: TXT
Series
Accession:
GSE186001
ID:
200186001
13.

The chromatin and single-cell transcriptional landscapes of CD4 T cells in inflammatory bowel disease link risk loci with a proinflammatory Th17 cell population

(Submitter supplied) Objective The imbalance between Th17 cells and regulatory T cells in the gut of inflammatory bowel disease (IBD) patients promotes intestinal epithelial cell damage. In this scenario, T helper cell lineage commitment is accompanied by dynamic changes to the chromatin that facilitate, enforce or repress gene expression patterns and ultimately promote the induction and maintenance of dysregulated intestinal CD4 T cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: TXT
Series
Accession:
GSE226875
ID:
200226875
14.

H3K27ac BL HiChIP and GRID-seq data of LW and MS

(Submitter supplied) For Large White (LW) and Meishan (MS) skeletal muscle, we performed H3K27ac BL HiCHIP to establish enhancer-promoter interaction maps. We also performed GRID-seq which uses a bivalent linker to ligate RNA to DNA in situ.
Organism:
Sus scrofa
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL19176
12 Samples
Download data: BEDPE, MCOOL, TXT
Series
Accession:
GSE189397
ID:
200189397
15.

A compendium map of Cis-Regulatory Elements in the Pig Genome and epigenetic comparison with the human Genome

(Submitter supplied) Although major advances in genomics have initiated an exciting new era of research, the lack of information about cis-regulatory elements has limited the genetic improvement or manipulation of pig as meat source and biomedical model. Here, we systematically characterize the cis-regulatory elements and their functions in the pig genome in 12 diverse tissues from 4 pig breeds through RNA-Seq, ATAC-Seq, and ChIP-Seq analyses. more...
Organism:
Sus scrofa
Type:
Other; Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL22918
200 Samples
Download data: BED, BEDGRAPH, BIGWIG, NARROWPEAK
Series
Accession:
GSE143288
ID:
200143288
16.

Whole Blood Transcriptome Profiling in Juvenile Idiopathic Arthritis and Inflammatory Bowel Disease

(Submitter supplied) We report whole blood gene expression of 12 healthy controls and 190 patients with either oligoarticular (n=43), polyarticular (n=46), or systemic JIA (n=26), or Crohn's disease (n=60) and ulcerative colitis (n=15). The subtypes of JIA are characterized by a gradient of differential gene expression ranging from controls to oligoJIA, polyJIA, sJIA, and IBD.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
202 Samples
Download data: TXT
17.

Genome-wide enhancer maps link disease variants to genes and cell types

(Submitter supplied) We generated ATAC-seq and H3K27ac ChIP-seq data in immortalized immune cancer cell lines to predict enhancer-gene regulation using the ABC model.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
67 Samples
Download data: TDF
Series
Accession:
GSE155555
ID:
200155555
18.

Transcriptomic profiling of THP-1 stable cell lines overexpressing genes associated with inflammatory bowel diseases (IBD)

(Submitter supplied) More than 200 genomic loci have been identified and validated by GWAS to be associated with IBD. However, for most of these loci, the causal gene remains unknown. The current study is aimed at uncovering the role of genes located within IBD-associated loci and endogenously expressed in the myeloid cell model THP-1 by over-expressing them in this cell lineage. The open reading frames (ORF) for 42 genes from IBD-associated loci were expressed in the THP-1 model of human monocytes using lentivirus vector for plasmid transduction. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
143 Samples
Download data: TXT
19.

Genetic and dietary modulators of inflammation in the gastro-intestinal tract of BXD genetic reference population

(Submitter supplied) Transcriptome data measured by microarray in colon of the BXD mouse genetic diversity model under a standard chow or a high fat diet at a fastd state.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL23038
99 Samples
Download data: CEL
Series
Accession:
GSE225791
ID:
200225791
20.

A functional genomics predictive network model identifies regulators of inflammatory bowel disease: Microarray Analysis of Human Blood and Intestinal Biopsy Samples from a Phase 2b, Double-blind, Placebo-controlled Study of Ustekinumab in Crohn's Disease

(Submitter supplied) Microarray Analysis of Human Whole Blood and Intestinal Biopsy Samples from a Phase 2b, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study of Ustekinumab in Crohn’s Disease
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
1717 Samples
Download data: CEL
Series
Accession:
GSE100833
ID:
200100833
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