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Items: 1 to 20 of 11682

1.

Activation of feedforward wiring in adult hippocampal neurons by the bHLH transcription factor Ascl4

(Submitter supplied) Although evidence indicates that the adult brain retains a considerable capacity for circuit formation, adult wiring has not been broadly considered and remains poorly understood. Here, we investigated wiring activation in adult neurons. Based on bioinformatic analyses on a previously published dataset (GSE161619), we identified the basic-helix-loop-helix (bHLH) transcription factor Ascl4 as a potential regulator of adult wiring and show that the AAV-mediated overexpression of Ascl4 can cell autonomously induce wiring in different types of hippocampal neurons of adult mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
228 Samples
Download data: TSV
Series
Accession:
GSE246825
ID:
200246825
2.

Responders to immune checkpoint therapy display early clonal expansion of tumour-infiltrating lymphocytes

(Submitter supplied) Using murine models that exclude variation in host genetics, environmental factors and tumour mutation burden, limiting variation between animals to naturally diverse TCRβ repertoires, we applied bulk TCRseq to study TCRβ repertoire dynamics in ICT responders and non-responders
Organism:
Mus musculus
Type:
Other
Platform:
GPL16417
225 Samples
Download data: TSV
Series
Accession:
GSE222575
ID:
200222575
3.

An epigenetic gene signature underlies phenotype switching in early stage melanomas.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Protein profiling by protein array; Expression profiling by array
Platforms:
GPL18573 GPL32055 GPL32054
300 Samples
Download data: BW, RCC, SF
Series
Accession:
GSE198432
ID:
200198432
4.

An epigenetic gene signature underlies phenotype switching in early stage melanomas [nanotstring_sample2]

(Submitter supplied) A 122-epigenetic gene signature distinguished low- versus high-risk early stage melanomas. We sought to validate the signature, examined clinical correlates in a cohort of primary melanomas of the skin, and studied the underlying transcriptomic aberrations and changes in chromatin in cell lines representing these two groups.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL32055
124 Samples
Download data: RCC
Series
Accession:
GSE198430
ID:
200198430
5.

Super-silencer perturbation by EZH2 and REST inhibition leads to large loss of chromatin interactions and reduction in cancer growth

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL20795 GPL24676 GPL20301
105 Samples
Download data: BED, HIC, TAB, TSV, TXT
Series
Accession:
GSE193489
ID:
200193489
6.

Shared patterns of glial transcriptional dysregulation link Huntington's disease and schizophrenia

(Submitter supplied) Huntington’s disease (HD) and juvenile-onset schizophrenia (SCZ) have long been regarded as distinct disorders. However, both manifest cell-intrinsic abnormalities in glial differentiation, with resultant astrocytic dysfunction and hypomyelination. To assess whether a common mechanism might underlie the similar glial pathology of these otherwise disparate conditions, we utilized comparative correlation network approaches to analyze RNA-seq data from human glial progenitor cells (hGPCs) produced from disease-derived pluripotent stem cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Third-party reanalysis
Platforms:
GPL18573 GPL16791
139 Samples
Download data: BW, NARROWPEAK
Series
Accession:
GSE188561
ID:
200188561
7.

Shared patterns of glial transcriptional dysregulation link Huntington's disease and schizophrenia

(Submitter supplied) Huntington’s disease (HD) and juvenile-onset schizophrenia (SCZ) have long been regarded as distinct disorders. However, both manifest cell-intrinsic abnormalities in glial differentiation, with resultant astrocytic dysfunction and hypomyelination. To assess whether a common mechanism might underlie the similar glial pathology of these otherwise disparate conditions, we utilized comparative correlation network approaches to analyze RNA-seq data from human glial progenitor cells (hGPCs) produced from disease-derived pluripotent stem cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
137 Samples
Download data: TXT
Series
Accession:
GSE188558
ID:
200188558
8.

Genomic context-dependent histone H3K36 methylation by Drosophila methyltransferases

(Submitter supplied) How different histone methyltransferases (HMT) cooperate to progressively catalyze different methylation states of the same residue as well the functional consequences of the different methylation states are not well known. Here, we address in the context of Drosophila H3K36 methylation by using single and combinatorial RNAi of HMTs along with genome-wide MNase-ChIPseq analyses. Our study reveals that K36me1/2/3 each mark distinct chromatin compartments. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL33093 GPL19951
107 Samples
Download data: BED, BW, TXT
Series
Accession:
GSE253391
ID:
200253391
9.

Single-cell transcriptome profiling of zebrafish pancreatic beta-cells segregated by CaMPARI-based calcium labeling.

(Submitter supplied) Coordination of cell activity trough Ca2+ waves enables pancreatic β-cells to secrete precise quantities of insulin in response to blood sugar. However, how the coordinating Ca2+ waves are orchestrated in space and time remains unknown. By applying functional Ca2+ imaging using CaMPARI and single-molecule RNA detection, we reveal a gene-signature depicting a molecularly and metabolically distinct state of first responder β-cells. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20828
191 Samples
Download data: CSV
Series
Accession:
GSE237867
ID:
200237867
10.

Multimodal measurement of the transcriptome and proteome in single cells using nanoSPLITS

(Submitter supplied) We report the development of a method (nanoSPLITS) capable of performing global proteome and transcriptome measurements from the same single-cell.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21697
192 Samples
Download data: TXT
Series
Accession:
GSE247519
ID:
200247519
11.

Transcriptome-wide characterization of genetic perturbations

(Submitter supplied) Single cell CRISPR screens such as Perturb-seq enable transcriptomic profiling of cellular perturbations at scale. However, the data produced by these screens are inherently noisy, limiting power to detect true effects with conventional differential expression analyses. Here, we introduce TRanscriptome-wide Analysis of Differential Expression (TRADE), a statistical framework which estimates the transcriptome-wide distribution of true differential expression effects from noisy gene-level measurements.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
224 Samples
Download data: H5AD, MTX, TSV
Series
Accession:
GSE264667
ID:
200264667
12.

A myeloid maturation program initiated by nucleotide depletion during S phase [RNA-Seq]

(Submitter supplied) Certain cancers, such as acute myeloid leukemia (AML), are caused by malignant stem cells that fail maturation. We sought to mechanistically understand how metabolism might regulate cell fate decisions and to identify metabolic differentiation agents that might be leveraged therapeutically.  We find that nucleotide – purine, pyrimidine, and deoxynucleotide – depletion leads to AML differentiation by way of replication stress. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
4 related Platforms
158 Samples
Download data: CSV, TSV
Series
Accession:
GSE172333
ID:
200172333
13.

Nucleotide depletion promotes cell fate transitions by inducing DNA replication stress

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
5 related Platforms
284 Samples
Download data: BW, CSV, MTX, TXT
Series
Accession:
GSE172335
ID:
200172335
14.

A set of circulating microRNAs belonging to the 14q32 chromosomic locus identifies two different subgroups of individuals with recent onset Stage 3 type 1 diabetes [second cohort, untargeted]

(Submitter supplied) Circulating microRNAs are linked to the onset and progression of type 1 diabetes mellitus (T1DM), making them potential biomarkers for the disease. In this study, we employ a multiplatform sequencing approach to analyze circulating microRNAs in an extended cohort of individuals with T1DM from the INNODIA consortium. Our findings reveal that a set of microRNAs located within the T1DM susceptibility chromosomal locus 14q32 distinguishes two subgroups of individuals. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL24676
154 Samples
Download data: CSV
Series
Accession:
GSE265981
ID:
200265981
15.

A set of circulating microRNAs belonging to the 14q32 chromosomic locus identifies two different subgroups of individuals with recent onset Stage 3 type 1 diabetes [first cohort, untargeted]

(Submitter supplied) Circulating microRNAs are linked to the onset and progression of type 1 diabetes mellitus (T1DM), making them potential biomarkers for the disease. In this study, we employ a multiplatform sequencing approach to analyze circulating microRNAs in an extended cohort of individuals with T1DM from the INNODIA consortium. Our findings reveal that a set of microRNAs located within the T1DM susceptibility chromosomal locus 14q32 distinguishes two subgroups of individuals. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL24676
121 Samples
Download data: CSV
Series
Accession:
GSE265980
ID:
200265980
16.

A set of circulating microRNAs belonging to the 14q32 chromosomic locus identifies two different subgroups of individuals with recent onset Stage 3 type 1 diabetes [first cohort, targeted]

(Submitter supplied) Circulating microRNAs are linked to the onset and progression of type 1 diabetes mellitus (T1DM), making them potential biomarkers for the disease. In this study, we employ a multiplatform sequencing approach to analyze circulating microRNAs in an extended cohort of individuals with T1DM from the INNODIA consortium. Our findings reveal that a set of microRNAs located within the T1DM susceptibility chromosomal locus 14q32 distinguishes two subgroups of individuals. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18573
119 Samples
Download data: CSV
Series
Accession:
GSE265976
ID:
200265976
17.

Persistent organic pollutants dysregulate energy homeostasis in human ovaries in vitro

(Submitter supplied) Exposure to persistent organic pollutants (POPs), such as dichlorodiphenyltrichloroethane (DDT) and polychlorinated biphenyls (PCBs), has historically been linked to population collapses in wildlife. Despite international regulations, these legacy chemicals are still currently detected in women of reproductive age, and their levels correlate with reduced ovarian reserve, longer time-to-pregnancy, and higher risk of infertility. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21697
242 Samples
Download data: TXT
Series
Accession:
GSE252776
ID:
200252776
18.

Combination of a SOS1-KRAS interaction inhibitor with a KRASG12C inhibitor combination can address intrinsic and acquired resistance leading to stronger and more durable response

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL30173
217 Samples
Download data: TSV
Series
Accession:
GSE225061
ID:
200225061
19.

Characterisation of the epidermal diurnal and circadian transcriptomes of mice with tissue-specific circadian clock activity

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
216 Samples
Download data
Series
Accession:
GSE190035
ID:
200190035
20.

Mutant IDH inhibitors induce lineage differentiation in IDH-mutant Oligodendroglioma II

(Submitter supplied) A subset of patients with IDH-mutant glioma respond to inhibitors of mutant IDH (IDHi), yet the molecular underpinnings of such responses are not understood. Here, we profiled by single-cell or single-nucleus RNA-sequencing three IDH-mutant oligodendrogliomas from patients who derived clinical benefit from IDHi. Importantly, the tissues were sampled on-drug, four weeks from treatment initiation. We further integrate our findings with analysis of single-cell and bulk transcriptomes from independent cohorts and experimental models. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL30172
141 Samples
Download data: TSV
Series
Accession:
GSE260933
ID:
200260933
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