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Links from GEO DataSets

Items: 19

1.
Full record GDS4283

Effect of lifestyle on Moroccan Amazighs: peripheral blood leukocytes

Analysis of leukocytes from regionally distinct groups of Moroccan Amazighs leading diverse lifestyles: nomadic, rural, and urban. The Amazighs represent a genetically relatively homogeneous population. Results provide insight into effect of environment on immune function and disease susceptibility.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 gender, 3 individual sets
Platform:
GPL5764
Series:
GSE8847
46 Samples
Download data: TXT
2.

The Effect of Lifestyle on Gene Expression in Moroccan Amazighs

(Submitter supplied) The human transitions from nomadic to agrarian to urban lifestyles are likely to impact physiology and disease susceptibility. In order to estimate the magnitude of the impact of lifestyle on genome function, we profiled gene expression in total leukocytes of Moroccan Amazigh from three distinct localities. Despite great expression heterogeneity in humans, as much as one third of the PBMC transcriptome was found to differ between the localities. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4283
Platform:
GPL5764
46 Samples
Download data: TXT
Series
Accession:
GSE8847
ID:
200008847
3.

Geographical Genomics of Human Leukocytes Gene Expression Variation

(Submitter supplied) Genome-wide association studies of transcript abundance in peripheral blood samples or derivative cell lines have demonstrated a preponderance of eSNP effects that, for the most part, involve regulatory polymorphisms in the differentially expressed gene. Several of these highlight associations that contribute to a variety of disease conditions, but the question arises as to how the associations are affected by the environment. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
194 Samples
Download data: TXT
Series
Accession:
GSE17065
ID:
200017065
4.

Differential methylation analysis in human whole blood DNA from healthy smokers and non-smokers

(Submitter supplied) To better characterize smoking–associated methylation changes in whole blood, we used Illumina HumanMethylation450 BeadChip to assess DNA samples from current (SM, n=172) and never smokers (NS, n=81).
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
253 Samples
Download data: IDAT, TXT
Series
Accession:
GSE85210
ID:
200085210
5.

Genome-wide DNA methylation map reveals widespread epigenetic variation in healthy individuals (RNA-Seq)

(Submitter supplied) Using neutrophils from a cohort of normal individuals, we generated transcriptomic profile of 4 individuals.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: XLSX
6.

Genome-wide DNA methylation map reveals widespread epigenetic variation in healthy individuals (RRBS)

(Submitter supplied) Using neutrophils from a cohort of normal individuals, we generated base-resolution DNA methylation maps to document inter-individual epigenetic variation.
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL11154
13 Samples
Download data: TXT, XLSX
Series
Accession:
GSE59163
ID:
200059163
7.

methylatedDNA_peripheralBlood

(Submitter supplied) The goal of the experiment – genome-wide profiling of DNA methylation reveals a class of normally methylated CpG island promoters Keywords: DNA methylation, Methylated CpG island amplification coupled with promoter arrays, normal tissue
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
4 related Platforms
4 Samples
Download data
Series
Accession:
GSE8810
ID:
200008810
8.

Single-base resolution DNA methylation profiles of two highly inbred chicken lines, Leghorn and Fayoumi, by whole-genome bisulfite sequencing (MethylC-seq).

(Submitter supplied) Here we provided the first single-base resolution DNA methylatome in chicken lungs by whole-genome bisulfite sequencing (MethylC-seq). In addition, two genetically distinct highly inbred chicken lines, Leghorn and Fayoumi, were used to examine how DNA methylation regulates mRNA gene expression between two lines. The methylation profile demonstrated that methylcytosines in the chicken were more likely to occur in CG dinucleotides than in non-CG sites. more...
Organism:
Gallus gallus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL9385
2 Samples
Download data: TXT
Series
Accession:
GSE56975
ID:
200056975
9.

Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia

(Submitter supplied) B-cell precursor acute lymphoblastic leukemia (pre-B ALL) is the most common pediatric cancer. Although the genetic origin of the disease remains unclear, epigenetic modifications including DNA methylation are suggested to contribute significantly to leukemogenesis. We assessed the DNA methylation status of 402,842 CpG-sites across the genome (Illumina 450k array) in tumor and remission samples of 46 pre-B ALL patients, thus generating the most comprehensive single CpG-site resolution pre-B ALL methylomes so far. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
92 Samples
Download data: TXT
Series
Accession:
GSE38235
ID:
200038235
10.

Genome-wide DNA methylation profile analysis of human intervertebral disc degeneration

(Submitter supplied) The pathophysiology of intervertebral disc (IVD) degeneration is not entirely understood; however, environmental and endogenous factors under genetic predisposition are considered to initiate the degenerative changes of human IVDs. Aberrant epigenetic alterations play a pivotal role in several diseases, including osteoarthritis. However, epigenetic alternations, including DNA methylation, in IVD degeneration have not been evaluated. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL21145
16 Samples
Download data: IDAT, TXT
Series
Accession:
GSE129789
ID:
200129789
11.

Mapping of variable DNA methylation across multiple cell types defines a dynamic regulatory landscape of the human genome

(Submitter supplied) DNA methylation is an important epigenetic modification involved in many biological processes and diseases. Many studies have mapped DNA methylation changes associated with embryogenesis, cell differentiation and cancer at a genome-wide scale. Our understanding of genome-wide DNA methylation changes in a developmental or disease-related context has been steadily growing. However, the investigation of which CpGs are variably methylated in different normal cell or tissue types is still limited. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing; Third-party reanalysis
Platforms:
GPL9115 GPL11154
31 Samples
Download data: TXT
Series
Accession:
GSE69894
ID:
200069894
12.

DNA methylation Profiling in Kawasaki disease (KD): DNA methylation profile in healthy control subjects, acute-phase KD subjects and convalescent-phase KD subjects

(Submitter supplied) DNA methylation analysis of DNA samples from total WBC collection The DNA samples from each subject was first subject to bisulfite conversion, followed by sample preparation and microarray experiment.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
36 Samples
Download data: IDAT
Series
Accession:
GSE109430
ID:
200109430
13.

Exon Level Expression Profiling in Kawasaki disease (KD): gene expression profile in healthy control subjects, acute-phase KD subjects and convalescent-phase KD subjects

(Submitter supplied) Transcriptome analysis of pooled RNA samples from total WBC collection The RNA samples from six subjects were evenly pooled into one pooled one, followed by sample preparation and microarray experiment.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17586
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE109351
ID:
200109351
14.

Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases

(Submitter supplied) The most common congenital heart disease (CHD) is the ventricular septal defect (VSD), which is also a subfeature of Tetralogy of Fallot (TOF) representing the most common form of cyanotic CHD. The underlying causes for the majority of CHDs are still unclear and most probably consist of combinations of genetic, epigenetic and environmental factors. DNA methylation is the most widely studied epigenetic modification and several cardiac regulators have already been shown to be differentially methylated in CHD patients. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL11154
23 Samples
Download data: TXT
Series
Accession:
GSE62629
ID:
200062629
15.

mRNA expression profiling in patients with Tetralogy of Fallot and healthy unaffected individuals

(Submitter supplied) Right ventricular mRNA profiles from 22 patients with Tetralogy of Fallot (TOF) and mRNA-seq profiles from the left and right ventricle (LV and RV, respectively) of 4 healthy unaffected individuals (NH) were generated. The total RNA was isolated from the 30 human heart samples using TRIzol. mRNAs were isolated from total RNA and prepared for sequencing using Illumina Kit RS-100-0801 according to the manufacturer's protocol (Preparing Samples for Sequencing of mRNA Sept 2008). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9052
30 Samples
Download data: TXT
Series
Accession:
GSE36761
ID:
200036761
16.

DNA methylation profiling of whole blood and reconstructed mixtures of purified leukocytes isolated from human adult blood

(Submitter supplied) Confounding due to cellular heterogeneity represents one of the foremost challenges currently facing Epigenome-Wide Association Studies (EWAS). Statistical methods leveraging the tissue-specificity of DNA methylation for deconvoluting the cellular mixture of heterogeneous biospecimens such as whole blood, offer a promising solution. However, their performance depends entirely on the library of DNA methylation markers being used as the basis for deconvolution. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
18 Samples
Download data: IDAT, TXT
Series
Accession:
GSE77797
ID:
200077797
17.

Genome wide DNA methylation in oral squamous cell carcinoma (OSCC) disease and adjacent normal tissue samples

(Submitter supplied) Genome wide DNA methylation profiling of normal and adjacent OSCC samples. The Illumina Infinium 450k Human DNA methylation Beadchip v1.2 was used to obtain DNA methylation profiles across approximately 4,50,000 CpGs in tissue samples. Total 21 samples were taken including 10 paired and 1 unpaired tissues. 6 were HPV Positive and 5 were HPV negative.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
21 Samples
Download data: IDAT
Series
Accession:
GSE87053
ID:
200087053
18.

Blood-Informative Transcripts Define Nine Common Axes of Peripheral Blood Gene Expression

(Submitter supplied) Whole peripheral blood samples collected into Tempus tubes from 189 adult participants in the Center for Health Discovery and Well Being study of Emory University and Georgia Tech, in Midtown Atlanta. The sample is of mixed ethnicity, and is part of a survey of the impact of genetics and lifestyle on gene expression and clinical attributes. Sample annotations include gender, self-reported ethnicity, zipcode of current address, and percent body fat, as well as technical features of the study (Sentrix plate ID, date of hybridization, and RNA quality RIN score.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
189 Samples
Download data: TXT
Series
Accession:
GSE35846
ID:
200035846
19.

Using Blood-Informative Transcripts in Geographical Genomics: Impact of Lifestyle on Gene Expression in Fijians

(Submitter supplied) This study explores the impact of lifestyle and environment on gene expression through whole transcriptome profiling of peripheral blood samples in Fijian population (native Melanesians and Indians) living in the rural and urban areas.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
41 Samples
Download data: TXT
Series
Accession:
GSE41233
ID:
200041233
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