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Links from GEO DataSets

Items: 20

1.

Generate 3D genome database for atrial and ventricles and using chamber selective chromatin loops link a subset of CSEs to target genes

(Submitter supplied) Measurement the contribution of 3D genome structure to chamber specific transcriptional programs and CSE activity.
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
6 Samples
Download data: TXT
Series
Accession:
GSE215020
ID:
200215020
2.

Regulation of mouse chamber selective enhancers

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other; Expression profiling by high throughput sequencing
Platforms:
GPL19057 GPL26526 GPL24247
82 Samples
Download data: BW, TXT
Series
Accession:
GSE215065
ID:
200215065
3.

Chamber selective enhancers identified in vivo by AAV-MPRA

(Submitter supplied) Measurement the activity of candidate CSEs in aCMs and vCMs.
Organism:
Mus musculus; synthetic construct
Type:
Other
Platforms:
GPL26526 GPL24247
15 Samples
Download data: TXT
Series
Accession:
GSE215033
ID:
200215033
4.

Dense, systematic mutagenesis to identify the features required for CSEs

(Submitter supplied) Investigate the sequence features required for CSE activity and selectivity.
Organism:
Mus musculus; synthetic construct
Type:
Other
Platforms:
GPL26526 GPL24247
14 Samples
Download data: TXT
Series
Accession:
GSE215032
ID:
200215032
5.

Transposase-accessible chromatin with high-throughput sequencing for purified neonatal aCMs and vCMs

(Submitter supplied) Examination of chamber selective chromatin accessibility and investigate if chromatin accessibility regulates CSEs.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
4 Samples
Download data: BW
Series
Accession:
GSE215031
ID:
200215031
6.

Next-generation sequencing facilitates quantitative analysis of atrial and ventricular cardiomyocytes transcriptomes

(Submitter supplied) To investigate the chamber selective transcriptional programs, we performed RNA-seq on purified cardiomyocytes. Totally we have 5 replicates for atrial cardiomyocytes and 5 replicates for ventricular cardiomyocytes.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
10 Samples
Download data: TXT
Series
Accession:
GSE215021
ID:
200215021
7.

BioChIP-seq analysis of atrial and ventricular cardiomyocytes

(Submitter supplied) Cardiac TF and P300 chromatin occupancy in atria and ventricles.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
33 Samples
Download data: BW
Series
Accession:
GSE215019
ID:
200215019
8.

Cardiac transcription factors in HL-1 cells: gene expression and genome binding profiling

(Submitter supplied) [1] Gene expression profiling in Gata4, Mef2a knockdown in HL-1 cells. HL-1 cells infected with adenovirus expressing either control siRNA or Gata4, and Gata4 & Mef2a siRNA. [2] Genome-wide maps of cardiac transcription factors binding region in HL-1 cells. We performed bio-ChIP-seq using streptavidin beads immunoprecipitation of biotinylated 5 cardiac transcription factors (fbio) and P300 antibody ChIP-seq. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9185 GPL6246
17 Samples
Download data: CEL, GFF, TXT
9.

A reference map of cardiac transcription factor chromatin occupancy identifies dynamic and conserved transcriptional enhancers

(Submitter supplied) Mapping the chromatin occupancy of transcription factors (TFs) is a key step in deciphering the transcriptional programs that orchestrate organ development and homeostasis. Here we used biotinylated knockin alleles of seven key TFs (GATA4, NKX2-5, MEF2A, MEF2C, SRF, TBX5, TEAD1) that regulate heart development and homeostasis to sensitively and reproducibly map their genome-wide occupancy in the fetal and adult heart. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL19057 GPL13112
45 Samples
Download data: BED, BW, TXT
Series
Accession:
GSE124008
ID:
200124008
10.

Characterization the crosstalk between P300 enhancers and 3D genome in murine cardiomyocyte development and maturation by H3K27ac HiChIP.

(Submitter supplied) We report the application of bioChIP-seq, bulk RNA-seq, Hi-C, H3K27ac HiChIP, and Massively parallel reporter assays (MPRAs) to characterize the p300-bound regulatory regions in murine cardiomyocytes (CMs). By obtaining ChIP-seq data of coactivator p300 from seven developmental stages of mouse CMs, we defined the dynamic p300 enhancers from embryonic CMs to adult CMs. We then validated the activity of dynamic p300 enhancers with AAV9-based MPRAs, we found dynamic p300 enhancers show dynamic activity from postnatal day 0 (P0) CMs to 4-week-old CMs. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
4 Samples
Download data: TXT
Series
Accession:
GSE222160
ID:
200222160
11.

Characterization of maturational enhancer activity by massively parallel reporter assay [amplicon-Seq]

(Submitter supplied) The activity of enhancers with dynamic P300 binding or mutagenized nuclear receptor motifs was assessed by massively parallel reporter assay during CM maturation.
Organism:
Mus musculus; Adeno-associated virus 9
Type:
Other
Platforms:
GPL31917 GPL19057
88 Samples
Download data: CSV
Series
Accession:
GSE196346
ID:
200196346
12.

Characterization of dynamic p300 enhancers in murine cardiomyocyte development

(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; Other
Platforms:
GPL21103 GPL19057 GPL24247
48 Samples
Download data: TXT
Series
Accession:
GSE195905
ID:
200195905
13.

Characterization of dynamic p300 enhancers in murine cardiomyocyte development [RNA-seq]

(Submitter supplied) We report the application of bioChIP-seq, bulk RNA-seq, Hi-C, and Massively parallel reporter assays (MPRAs) to characterize the p300-bound regulatory regions in murine cardiomyocytes (CMs). By obtaining ChIP-seq data of coactivator p300 from seven developmental stages of mouse CMs, we defined the dynamic p300 enhancers from embryonic CMs to adult CMs. We then validated the activity of dynamic p300 enhancers with AAV9-based MPRAs, we found dynamic p300 enhancers show dynamic activity from postnatal day 0 (P0) CMs to 4-week-old CMs. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
21 Samples
Download data: TXT
Series
Accession:
GSE195902
ID:
200195902
14.

Characterization of dynamic p300 enhancers in murine cardiomyocyte development [ChIP-seq]

(Submitter supplied) We report the application of bioChIP-seq, bulk RNA-seq, Hi-C, and Massively parallel reporter assays (MPRAs) to characterize the p300-bound regulatory regions in murine cardiomyocytes (CMs). By obtaining ChIP-seq data of coactivator p300 from seven developmental stages of mouse CMs, we defined the dynamic p300 enhancers from embryonic CMs to adult CMs. We then validated the activity of dynamic p300 enhancers with AAV9-based MPRAs, we found dynamic p300 enhancers show dynamic activity from postnatal day 0 (P0) CMs to 4-week-old CMs. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
14 Samples
Download data: BIGWIG
Series
Accession:
GSE195901
ID:
200195901
15.

Characterization of dynamic p300 enhancers in murine cardiomyocyte development [HiC]

(Submitter supplied) We report the application of bioChIP-seq, bulk RNA-seq, Hi-C, and Massively parallel reporter assays (MPRAs) to characterize the p300-bound regulatory regions in murine cardiomyocytes (CMs). By obtaining ChIP-seq data of coactivator p300 from seven developmental stages of mouse CMs, we defined the dynamic p300 enhancers from embryonic CMs to adult CMs. We then validated the activity of dynamic p300 enhancers with AAV9-based MPRAs, we found dynamic p300 enhancers show dynamic activity from postnatal day 0 (P0) CMs to 4-week-old CMs. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL21103
9 Samples
Download data: COOL
Series
Accession:
GSE194087
ID:
200194087
16.

Genome-wide chromatin state in non-failing and dilated cardiomyaphty human left ventricles

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20301
30 Samples
Download data
Series
Accession:
GSE135956
ID:
200135956
17.

Genome-wide chromatin state in non-failing and dilated cardiomyaphty human left ventricles [PLAC-seq]

(Submitter supplied) We conducted chromatin immunoprecipitation followed by sequencing (ChIP-seq) and proximity ligation-assisted ChIP-seq (PLAC-seq) for enhancers and promoters (E-P) using left ventricular tissues from dilated cardiomyopathy (DCM) patients and non-heart failure (NF) donors. Differential active enhancer H3K27ac and promoter H3K4me3 regions were identified between NF and DCM. While the average read density (ARD) for H3K27ac is similar between NF and DCM, the ARD of H3K4me3 is significantly lower in DCM samples than in NF.Super-enhancer (SE) analysis revealed that 929 and 129 genes linked to NF- and DCM-specific SE, respectively, and three unique SE-associated genes between NF and DCM were identified.Moreover, the differential E-P interactions were observed in the known heart failure gene loci and are correlated with the gene expression levels. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20301
8 Samples
Download data: HIC
Series
Accession:
GSE135954
ID:
200135954
18.

Genome-wide chromatin state in non-failing and dilated cardiomyaphty human left ventricles [ChIP-Seq]

(Submitter supplied) We conducted chromatin immunoprecipitation followed by sequencing (ChIP-seq) and proximity ligation-assisted ChIP-seq (PLAC-seq) for enhancers and promoters (E-P) using left ventricular tissues from dilated cardiomyopathy (DCM) patients and non-heart failure (NF) donors. Differential active enhancer H3K27ac and promoter H3K4me3 regions were identified between NF and DCM. While the average read density (ARD) for H3K27ac is similar between NF and DCM, the ARD of H3K4me3 is significantly lower in DCM samples than in NF.Super-enhancer (SE) analysis revealed that 929 and 129 genes linked to NF- and DCM-specific SE, respectively, and three unique SE-associated genes between NF and DCM were identified.Moreover, the differential E-P interactions were observed in the known heart failure gene loci and are correlated with the gene expression levels. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20301
22 Samples
Download data: BED
Series
Accession:
GSE135953
ID:
200135953
19.

Temporal Analyses of Cardiac Chromatin Accessibility, DNA Methylation and Epigenomic Structure Reveal Locus-Specific Regulation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL21493 GPL19057 GPL24247
47 Samples
Download data: BW, CGMAP, TAR
Series
Accession:
GSE154521
ID:
200154521
20.

Temporal Analyses of Cardiac Chromatin Accessibility, DNA Methylation and Epigenomic Structure Reveal Locus-Specific Regulation [RRBS]

(Submitter supplied) Heart failure can be induced or ameliorated by regulation of chromatin modifying enzymes. Because so many chromatin factors regulate gene expression, we used ATAC-seq to report the status of a given locus at any time—the sum total of all epigenetic modifiers—in a mouse model of pressure overload hypertrophy. Early compensation of pressure overload at 3 days was associated with widespread changes in chromatin accessibility and DNA methylation, the majority of which persisted to the decompensated phase (3 weeks), revealing the temporal nature of epigenomic compensation to pathologic stimuli. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platforms:
GPL24247 GPL21493
23 Samples
Download data: CGMAP
Series
Accession:
GSE154520
ID:
200154520
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