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Links from GEO DataSets

Items: 20

1.

Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta (RNA-seq)

(Submitter supplied) Given the possible critical importance of placental gene imprinting and random monoallelic expression on fetal and infant health, most of those genes must be identified, in order to understand the risks that the baby might meet during pregnancy and after birth. Therefore, the aim of the current study was to introduce a workflow and tools for analyzing imprinted and random monoallelic gene expression in human placenta, by applying whole-transcriptome (WT) RNA sequencing of placental tissue and genotyping of coding DNA variants in family trios. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16288
10 Samples
Download data: TXT
Series
Accession:
GSE56524
ID:
200056524
2.

Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array; Expression profiling by high throughput sequencing
Platforms:
GPL16288 GPL18544
40 Samples
Download data
Series
Accession:
GSE56781
ID:
200056781
3.

Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placenta (SNP genotyping)

(Submitter supplied) Given the possible critical importance of placental gene imprinting and random monoallelic expression on fetal and infant health, most of those genes must be identified, in order to understand the risks that the baby might meet during pregnancy and after birth. Therefore, the aim of the current study was to introduce a workflow and tools for analyzing imprinted and random monoallelic gene expression in human placenta, by applying whole-transcriptome (WT) RNA sequencing of placental tissue and genotyping of coding DNA variants in family trios. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platform:
GPL18544
30 Samples
Download data: TXT
Series
Accession:
GSE56685
ID:
200056685
4.

Global assessment of imprinted gene expression in the bovine conceptus by next generation sequencing

(Submitter supplied) Genomic imprinting is an epigenetic mechanism that leads to parental-allele-specific gene expression. Approximately 150 imprinted genes have been identified in humans and mice but less than 30 genes have been described as imprinted in cattle. For the purpose of de novo identification of imprinted genes in bovine, we determined global monoallelic gene expression in brain, skeletal muscle, liver, kidney and placenta of day ~105 Bos taurus indicus X Bos taurus taurus F1 conceptuses using RNA sequencing. more...
Organism:
Bos indicus; Bos indicus x Bos taurus
Type:
Expression profiling by high throughput sequencing; Genome variation profiling by high throughput sequencing
Platforms:
GPL21383 GPL20723
5 Samples
Download data: VCF, XLSX
Series
Accession:
GSE77389
ID:
200077389
5.

Allelic imbalance is a prevalent and tissue-specific feature of the mouse transcriptome

(Submitter supplied) We perform a systematic classification of allelic imbalance in mouse hybrids derived from reciprocal crosses of divergent strains. We observe that deviation from balanced biallelic expression is common, occurring in ~20% of the mouse transcriptome. Allelic imbalance attributed to genotype is by far the most prevalent class and typically is tissue-specific. However, some genotype-based imbalance is maintained across tissues and is associated with greater genetic variation, especially in 5’ and 3’ termini of transcripts. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL13112
11 Samples
Download data: BW
Series
Accession:
GSE58524
ID:
200058524
6.

Analysis of parent-of-origin bias in gene expression levels

(Submitter supplied) In order to study parent-of-origin effects on gene expression, we performed RNAseq analysis (100bp single end reads) of 165 children who formed part of mother/father/child trios where genotype data was available from the HapMap and/or 1000 Genomes Projects. Based on phased genotypes at heterozygous SNP positions, we generated allelic counts for expression of the maternal and paternal alleles in each individual. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
165 Samples
Download data: TXT
7.

Profiling of differential allelic expression in horse, donkey, mule and hinny placental tissue

(Submitter supplied) The discovery of genomic imprinting through studies of manipulated mouse embryos indicated that the paternal genome has a major influence on placental development. However, previous research has not demonstrated paternal bias in imprinted genes. We applied RNA sequencing to trophoblast tissue from reciprocal hybrids of horse and donkey, where genotypic differences allowed parent-of-origin identification of most expressed genes. more...
Organism:
Equus asinus x Equus caballus; Equus caballus; Equus caballus x Equus asinus; Equus asinus
Type:
Expression profiling by high throughput sequencing
4 related Platforms
4 Samples
Download data: SAM
Series
Accession:
GSE30243
ID:
200030243
8.

Allele-specific Methylation of Human Placental Tissue

(Submitter supplied) In this study, we screened human placental samples for allele-specific methylation and subsequently novel imprinted genes associated with these regions. We used reduced representation bisulfite sequencing to identify partially methylated CpG islands (CGIs) in the human placental genome. We were able to delineate potential candidates for allele-specific methylation based on the calculation of a concordance statistic. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL10999
10 Samples
Download data: TXT
9.

Profiling of differential allelic expression in mouse placenta from reciprocal crosses

(Submitter supplied) Many questions about the regulation, functional specialization, computational prediction, and evolution of genomic imprinting would be better addressed by having an exhaustive genome-wide catalog of genes that display parent-of-origin differential expression. As a first-pass scan for novel imprinted genes, we performed mRNA-seq experiments on E17.5 mouse placenta cDNA samples from reciprocal cross F1 progeny of AKR and PWD mouse strains, and quantified the allele-specific expression and the degree of parent-of-origin effect transcriptome-wide. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9185
2 Samples
Download data: SAM
Series
Accession:
GSE29690
ID:
200029690
10.

Placental gene expression profiling for the identification of clinically relevant subclasses of human preeclampsia

(Submitter supplied) Preeclampsia (PE) is a complex, heterogeneous disorder of pregnancy, demonstrating considerable variability in observed maternal symptoms and fetal outcomes. We hypothesized that this heterogeneity is due to the existence of multiple molecular forms of PE. To address our hypothesis, we created a large (N=330) human placental microarray data set consisting of seven previously published studies (GSE30186, GSE10588, GSE24129, GSE25906, GSE43942, GSE4707, and GSE44711) and 157 highly annotated samples from a BioBank (below). more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Third-party reanalysis
Platform:
GPL6244
157 Samples
Download data: CEL, CSV
Series
Accession:
GSE75010
ID:
200075010
11.

Characterization of global loss of imprinting in overgrowth syndrome induced by assisted reproduction

(Submitter supplied) Embryos generated with the use of assisted reproductive technologies (ART) can develop overgrowth syndromes. In ruminants, the condition is referred to as large offspring syndrome (LOS) and exhibits variable phenotypic abnormalities including overgrowth, enlarged tongue, and abdominal wall defects. These characteristics recapitulate those observed in the human loss-of-imprinting (LOI) overgrowth syndrome Beckwith-Wiedemann (BWS). more...
Organism:
Bos indicus x Bos taurus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21383
32 Samples
Download data: TXT
Series
Accession:
GSE63509
ID:
200063509
12.

A survey of imprinted gene expression in mouse trophoblast stem cells

(Submitter supplied) Several hundred mammalian genes are expressed preferentially from one parental allele due to a process called genomic imprinting. Genomic imprinting is particularly prevalent in extra-embryonic tissue, where it plays an essential role during development. Here, we profiled imprinted gene expression via RNA-Seq in a panel of six mouse trophoblast stem (TSC) lines, which are ex vivo derivatives of a progenitor population that gives rise to the placental tissue of the mouse. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: BED, TXT
Series
Accession:
GSE63968
ID:
200063968
13.

Genome-wide assessment of imprinted expression in human cells

(Submitter supplied) Parent-of-origin dependent expression of alleles, imprinting, has been suggested to impact a substantial proportion of mammalian genes. Its discovery requires allele-specific detection of expressed transcripts, but in some cases detected allelic expression (AE) bias has been interpreted as imprinting without demonstrating compatible transmission patterns and excluding heritable variation. Therefore, we utilized a genome-wide tool exploiting high density genotyping arrays in parallel measurements of genotypes in RNA and DNA to determine AE across the transcriptome in lymphoblastoid cell lines (LCLs) and skin fibroblasts derived from families.
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platforms:
GPL6984 GPL6983
112 Samples
Download data
Series
Accession:
GSE26286
ID:
200026286
14.

Parent-of-Origin Allelic Expression in the Mouse Cerebellum

(Submitter supplied) The maternal and paternal genomes play different roles in mammalian brains as a result of genomic imprinting, an epigenetic regulation leading to differential expression of the parental alleles of some genes. Here we investigate genomic imprinting in the cerebellum using a newly developed Bayesian statistical model that provides unprecedented transcript-level resolution. We uncover 160 imprinted transcripts, including 41 novel and independently validated imprinted genes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
48 Samples
Download data: CSV, GTF, XLSX
Series
Accession:
GSE67556
ID:
200067556
15.

Profiling of differential allelic expression in horse, donkey, mule, and hinny placental tissues.

(Submitter supplied) In eutherian mammals, dosage compensation of X-linked genes is achieved by X chromosome inactivation. X inactivation is random in embryonic and adult tissues, but imprinted X inactivation (paternal X silencing) has been identified in the extraembryonic membranes of the mouse, rat, and cow. Few other species have been studied for this trait, and the data from studies of the human placenta have been discordant or inconclusive. more...
Organism:
Equus caballus; Equus caballus x Equus asinus; Equus asinus; Equus asinus x Equus caballus
Type:
Expression profiling by high throughput sequencing
4 related Platforms
15 Samples
Download data: TXT
Series
Accession:
GSE36352
ID:
200036352
16.

Deciphering the genetic regulation of peripheral blood transcriptome in pigs through allele-specific expression analysis and expression genome-wide association study

(Submitter supplied) Efforts to improve resilience in livestock production systems have focused on two objectives: investigating the genetic control of immune function as it pertains to robustness and disease resistance, and finding predictive markers for use in breeding programs. In this context, the peripheral blood transcriptome represents an important source of biological information about an individual's health and immunological status, and has been proposed for use as an intermediate phenotype to measure immune capacity. more...
Organism:
Sus scrofa
Type:
Expression profiling by array
Platform:
GPL19893
243 Samples
Download data: TXT
Series
Accession:
GSE97374
ID:
200097374
17.

Estimates of total imprint number withstand transcriptome test

(Submitter supplied) The number of transcripts where allelic bias is dependent parent-of-origin was predicted at 100-200 until two recent studies applied RNA-Seq to brain regions from reciprocally crossed inbred mouse strains and identified over a thousand novel imprinted loci, including hundreds present in only males or females. Reanalysis revealed that the vast majority of these novel loci are explained by technical and biological variation of the approach, and are not genuine cases of general or sex-specific parent-of-origin allelic expression. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: BED, TXT
Series
Accession:
GSE27016
ID:
200027016
18.

The imprinted Phlda2 gene modulates a major endocrine compartment of the placenta to regulate placental demands for maternal resources

(Submitter supplied) Recent work suggests that imprinted genes may regulate the signalling function of the placenta by modulating the size of the endocrine compartment. Our work provides in vivo evidence that this hypothesis is well founded. Affymetrix Mouse Microarray analysis of E16.5 placneta was used to demonstrate gene expression changes in the mutant placenta.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
11 Samples
Download data: CEL
Series
Accession:
GSE74318
ID:
200074318
19.

Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data.

(Submitter supplied) Next-generation sequencing has become an important tool for genome-wide quantification of DNA and RNA. However, a major technical hurdle lies in the need to map short sequence reads back to their correct locations in a reference genome. Here we investigate the impact of SNP variation on the reliability of read-mapping in the context of detecting allele-specific expression (ASE).We generated sixteen million 35 bp reads from mRNA of each of two HapMap Yoruba individuals. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9115
2 Samples
Download data: MAP
20.

F1 Interspecies Hybrid Analysis Reveals Parent-Of-Origin Bias in the Mouse Placenta

(Submitter supplied) To investigate the epigenetic landscape at the interface between mother and fetus, we provide a comprehensive analysis of parent of origin bias in the placenta. Using F1 interspecies hybrids, we sequenced RNA from 23 individual midgestation placentas, five late stage placentas, and two yolk sac samples and then used SNPs to determine whether transcripts were preferentially generated from the maternal or paternal allele. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9250
31 Samples
Download data: BED
Series
Accession:
GSE42671
ID:
200042671
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