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Items: 1 to 20 of 139

1.

Temporal transcriptome changes in Drosophila eye development

(Submitter supplied) we have performed mRNA-Seq studies of the larval eye and antennal primordial at multiple timepoints within the third larval instar and white prepupal stages
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
12 Samples
Download data: XLSX
Series
Accession:
GSE164079
ID:
200164079
2.

Chromatin landscape changes of regenerating wing imaginal discs

(Submitter supplied) We report the changes in chromatin accessibility associated with regeneration in wing imaginal discs at two developmental timepoints during L3. Wing discs were ablated using tissue-specific expression of the pro-apoptotic gene eiger at an early timepoint (day 7) when the discs retain high regenerative capacity and at a late time point (day 9) when regenerative capacity has significantly declined. ATAC-seq was performed on these discs after 40 hr of ablation and compared to identically staged unablated discs. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21306 GPL9061
13 Samples
Download data: BED, BW, XLS
Series
Accession:
GSE140755
ID:
200140755
3.

Expression of E93 provides an instructive cue to control dynamic enhancer activity and chromatin accessibility during development

(Submitter supplied) How temporal cues combine with spatial inputs to control gene expression during development is poorly understood. Here, we test the hypothesis that the Drosophila transcription factor E93 controls temporal gene expression by regulating chromatin accessibility. Precocious expression of E93 early in wing development reveals that it can simultaneously activate and deactivate different target enhancers. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9061 GPL17275
39 Samples
Download data: BED, BW, CSV, NARROWPEAK
Series
Accession:
GSE141738
ID:
200141738
4.

Single-cyst transcriptome analysis of Drosophila male germline stem cell

(Submitter supplied) To elucidate endogenous gene expression profiles in germ cells at discrete but continuous differentiation stages, we developed a new experimental strategy that we named Transcriptome Analysis using Single Germline Cyst (TASC).
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL9061 GPL17275
19 Samples
Download data: XLSX
Series
Accession:
GSE142717
ID:
200142717
5.

Impact of CG5694/ova in Drosophila ovaries

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL9061 GPL17275
27 Samples
Download data: BW
Series
Accession:
GSE104925
ID:
200104925
6.

Impact of depeltion of CG5694/ova on transcription in Drosophila ovaries [miRNA- and RNA-seq]

(Submitter supplied) Purpose: To analysis Ova impact on transcription in Drosophila ovaries by mRNA-seq and small RNA-seq Methods: mRNA-seq and small RNA-seq of RNA extracted from Drosophila ovaries Results: Ova has no obvious impact on protein coding genes expression or piRNA biogenesis.
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL17275 GPL9061
12 Samples
Download data: TXT
Series
Accession:
GSE104924
ID:
200104924
7.

Integrative Genomic Analysis Reveals Novel Regulatory Mechanisms of eyeless During Drosophila Eye Development

(Submitter supplied) eyeless (ey) is one of the most critical transcription factors for initiating the entire eye development in Drosophila. However, the molecular mechanisms through which Ey regulates target genes and pathways have not been characterized at the genomic level. Using ChIP-Seq, we generated an endogenous Ey binding profile in Drosophila developing eyes. These data sets will serve as a valuable resource for future studies on Ey and eye development.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9061
8 Samples
Download data: WIG
Series
Accession:
GSE112868
ID:
200112868
8.

Remapping the SRA: Drosophila melanogaster RNA-Seq data from the Sequence Read Archive

(Submitter supplied) The sequence read archive (SRA) contains over 52 terabases or 482 billion reads from Drosophila melanogaster (as of June 2018). These data are massively underused by the community and include 14,423 RNA-Seq samples, that is roughly 7 times the size of modENCODE. Currently the major challenge is finding high quality datasets that are suitable for inclusion in new studies. To help the community overcome this hurdle, we re-processed all D. more...
Organism:
Drosophila melanogaster
Type:
Third-party reanalysis; Expression profiling by high throughput sequencing
18 related Platforms
14423 Samples
Download data: BW, GTF, TSV, TXT
Series
Accession:
GSE117217
ID:
200117217
9.

Predicting microRNA targeting efficacy in Drosophila

(Submitter supplied) A series of transfections was performed in Drosophila S2 cells to explore: 1) the types of target sites that Drosophila microRNAs recognize, 2) the relative functional efficacy of these sites in mediating repression, and 3) the determinants that allow some sites to have greater potency than others. 3p-seq was also performed to help reannotate and quantify the landscape of 3' UTRs in Drosophila S2 cells.
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
10 Samples
Download data: BED, TXT
Series
Accession:
GSE74581
ID:
200074581
10.

Twin-miRs and their many weak targets

(Submitter supplied) MicroRNAs (miRNA) are small, endogenous RNAs that regulate the expression of mRNAs posttranscriptionally. To identify miRNAs that produce twin products, we sequenced these five small RNA libraries and collected other published datasets to represent a systematic coverage of the major tissue types (head, body and sexual organs) in D. melanogaster. To survey the repression effects of twin miRs on the their targets, we dissected testes from adult flies that lacked Dm310s due to a knock-out mutation (Tang, et al. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL9061 GPL13304
9 Samples
Download data: FA, TXT, XLSX
Series
Accession:
GSE97364
ID:
200097364
11.

Temporally-regulated tRNA-derived small RNAs are associated primarily with non-polysomal fractions in Drosophila

(Submitter supplied) Eukaryotic genomes contain various types of small non-coding RNAs such as microRNAs (miRNAs), silencing RNAs (siRNAs) and PIWI-interacting RNAs (piRNAs). Recent studies point to the presence of a more diverse array of uncharacterized small regulatory RNAs including those that are generated from mRNAs, rRNAs and tRNAs. To explore the possible involvement of tRNA-derived fragments (tRFs) in translational regulation, we fractionated 1 and 8h Drosophila embryos on sucrose density gradients and quantitatively measured by deep-dequencing the expression levels of the tRFs in the fractionated and unfractionated Drosophila embryonic cytosolic extracts. more...
Organism:
Drosophila melanogaster
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL9061
10 Samples
Download data: FASTQ, TXT, XLS
Series
Accession:
GSE35443
ID:
200035443
12.

Genome-wide identification of Grainy head targets in Drosophila [ChIP-seq]

(Submitter supplied) Grainy head (Grh) is a conserved transcription factor (TF) controlling epithelial differentiation and regeneration. To elucidate Grh functions, we identified embryonic Grh targets by ChIP-seq and gene expression analysis. We show that Grh controls hundreds of target genes. Repression or activation correlates with the distance of Grh binding sites to the transcription start sites of its targets. Analysis of 54 Grh-responsive enhancers during development and upon wounding suggests cooperation with distinct TFs in different contexts. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9061
3 Samples
Download data: BED, FASTA
Series
Accession:
GSE102550
ID:
200102550
13.

Effect of receipt of male ejaculate sex peptide on micro RNA expression in female Drosophila melanogaster, 3 hours after the start of mating, in HeadThorax (HT) and Abdomen (Abd) tissues.

(Submitter supplied) Seminal fluid proteins (Sfps) can have significant effects on female behaviour and physiology. In Drosophila melanogaster a single Sfp, sex peptide (SP), triggers a remarkably diverse array of fundamentally important responses. It increases female fecundity, juvenile hormone (JH) production, antimicrobial peptide production and feeding rates, whilst decreasing sexual receptivity. Although these features are expected to leave a strong genomic signature, previous studies indicated that Sfps affect the expression of relatively modest numbers of genes. more...
Organism:
Drosophila melanogaster
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL9061
8 Samples
Download data
Series
Accession:
GSE31250
ID:
200031250
14.

Hormone-dependent control of developmental timing through regulation of chromatin accessibility

(Submitter supplied) We identify a temporal cascade of ecdysone-inducible transcription factor gene expression during Drosophila wing development. This temporal cascade corresponds with dynamic changes in chromatin accesibility during wing development. We hypothesized that these temporally regulated transcription factors may coordinate these dynamic open chromatin changes. To test this, we investigate the ecdysone-inducible transcription factor, E93, which we determine is required for coordinating transitions in developmental stage by regulating chromatin accesibility of cis-regulatory elements.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL9061 GPL17275
24 Samples
Download data: BED, BW, TXT, XLSX
Series
Accession:
GSE97956
ID:
200097956
15.

Integrative analysis unveils new functions for the Drosophila Cutoff protein in non-coding RNA biogenesis and gene regulation

(Submitter supplied) Piwi-Interacting RNAs (piRNAs) are central components of the piRNA pathway, which directs transposon silencing and guarantees genome integrity in the germ cells of several metazoans. In Drosophila, piRNAs are produced from discrete regions of the genome termed piRNA clusters, whose expression relies on the RDC complex comprised of the core proteins Rhino, Deadlock and Cutoff. To date, the RDC complex has been exclusively implicated in the regulation of the piRNA loci. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9061
17 Samples
Download data: BED, TXT
Series
Accession:
GSE98635
ID:
200098635
16.

Chromatin profiling of Drosophila CNS subpopulations identifies active transcriptional enhancers

(Submitter supplied) Transcriptional analysis of Drosophila CNS midline cells provides a useful system for studying transcriptional regulation at the genomic level due to a well-characterized set of midline-expressed genes and in vivo-validated enhancers. To investigate how access to regulatory information is controlled during midline cell development, we performed FAIRE-seq on FACS-purified midline cells. We find that regions of the genome with a strong midline FAIRE peak and weak whole-embryo FAIRE peak (“midline-enriched”) often correspond to midline enhancers near a midline-expressed gene and provides a useful predictive tool. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9061 GPL13304
5 Samples
Download data: BED, WIG
Series
Accession:
GSE83463
ID:
200083463
17.

mRNA Poly(A)-tail Changes Specified by Deadenylation Broadly Reshape Translation in Drosophila Oocytes and Early Embryos

(Submitter supplied) Because maturing oocytes and early embryos lack transcription, posttranscriptional regulatory processes must control their development. To better understand this control, we profiled translational efficiencies and poly(A)-tail lengths throughout Drosophila oocyte maturation and early embryonic development. The correspondence between translational-efficiency changes and tail-length changes indicated that tail-length changes broadly reshape translational activity until gastrulation, when this coupling disappears. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL9061 GPL17275
42 Samples
Download data: TXT
Series
Accession:
GSE83616
ID:
200083616
18.

ChIP-seq of MSL1 in male and female fly samples

(Submitter supplied) We report the binding of MSL1 protein in male, female and mof2 mutant samples of Drosophila melanogaster and Drosophila virilis
Organism:
Drosophila virilis; Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
4 related Platforms
10 Samples
Download data: BW
Series
Accession:
GSE61340
ID:
200061340
19.

High-Affinity Sites Form an Interaction Network to Facilitate Spreading of the MSL Complex across the X Chromosome in Drosophila

(Submitter supplied) Hi-C analysis of two Drosophila male cell lines, combined with 4C-seq of frequent long-range contacts between HAS.
Organism:
Drosophila melanogaster
Type:
Other; Genome binding/occupancy profiling by high throughput sequencing
4 related Platforms
100 Samples
Download data: BED, BIGWIG, BW, TXT
Series
Accession:
GSE58821
ID:
200058821
20.

The cis-regulatory code of Hox function in Drosophila

(Submitter supplied) Precise gene expression is a fundamental aspect of organismal function and depends on the combinatorial interplay of transcription factors (TFs) with cis‐regulatory DNA elements. While much is known about TF function in general, our understanding of their cell type‐specific activities is still poor. To address how widely expressed transcriptional regulators modulate downstream gene activity with high cellular specificity, we have identified binding regions for the Hox TF Deformed (Dfd) in the Drosophila genome. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9061
2 Samples
Download data: CSV
Series
Accession:
GSE73493
ID:
200073493
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