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Links from GEO DataSets

Items: 20

1.

Expression profiling pooled Drosophila melanogaster heterozygous for deletions on Chromosome 2L

(Submitter supplied) We performed mRNA transcriptional profiling on 99 hemizygotic lines (Df/+) from the DrosDel project covering 68% of chromosome 2L, in order to understand how changes in gene copy number affect overall transcriptome.
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13304
396 Samples
Download data: TXT
Series
Accession:
GSE61509
ID:
200061509
2.

Expression profiling individual DrosDel flies heterozygous for deletions of chromosome 2L in a hybrid background

(Submitter supplied) In order to understand the effect of genetic background on the response to gene dose perturbation, we performed mRNA transcriptional profiling on 99 hemizygotic lines (Df/+) from the DrosDel project, which have hybrid genetic background of OregonR/w1118.
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13304
417 Samples
Download data: TXT
Series
Accession:
GSE73920
ID:
200073920
3.

RNA-Seq of female, male, and sex-transformed Drosophila melanogaster heads from flies heterozygous for deletions on chromosome X and 3L

(Submitter supplied) To measure the response to gene dose, we performed mRNA-Seq of fly heads with molecularly defined deletions constructed from DrosDel deficiency lines (Ryder et al. Genetics 2007, 177(1):615-29) on the Illumina HiSeq 2000 platform.
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13304
249 Samples
Download data: TXT
Series
Accession:
GSE60571
ID:
200060571
4.

Differential Chromatin Binding of the Drosophila Dosage Compensation Complex

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by genome tiling array; Genome binding/occupancy profiling by high throughput sequencing
4 related Platforms
27 Samples
Download data: PAIR
Series
Accession:
GSE37865
ID:
200037865
5.

ChIP-Seq profiles of MSL1, MSL2, MSl3, MOF, MLE, H4K16ac and RNA Polymerase II phosphorlyated on Serine 5 in Drosophila S2 cells

(Submitter supplied) ChIP-Seq profiles of MSL1, MSL2, MSl3, MOF, MLE, H4K16ac and RNA Polymerase II phosphorlyated on Serine 5 in Drosophila S2 cells
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL13304 GPL9058 GPL9061
17 Samples
Download data: BEDGRAPH
Series
Accession:
GSE37864
ID:
200037864
6.

ChIP-chip profiles of MLE, MSL3 and MOF in Drosophila S2 cells

(Submitter supplied) ChIP-chip profiles of MLE, MSL3 and MOF in Drosophila S2 cells
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7107
10 Samples
Download data: PAIR
Series
Accession:
GSE37863
ID:
200037863
7.

X chromosome dosage compensation via enhanced transcriptional elongation in Drosophila males (Control & MSL2 RNAi)

(Submitter supplied) MSL (Male-specific lethal) complex increases transcription on the single X chromosome of Drosophila males in order to equalize expression of X-linked genes between males (XY) and females (XX). The increase in transcript levels correlates with MSL- dependent acetylation of histone H4 at K16 within the bodies of active genes, but identification of the transcriptional step affected has not been possible. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
12 Samples
Download data: TXT
Series
Accession:
GSE25887
ID:
200025887
8.

X chromosome dosage compensation via enhanced transcriptional elongation in Drosophila males (Untreated)

(Submitter supplied) MSL (Male-specific lethal) complex increases transcription on the single X chromosome of Drosophila males in order to equalize expression of X-linked genes between males (XY) and females (XX). The increase in transcript levels correlates with MSL- dependent acetylation of histone H4 at K16 within the bodies of active genes, but identification of the transcriptional step affected has not been possible. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
3 Samples
Download data: TXT
Series
Accession:
GSE25321
ID:
200025321
9.

RNA-seq data in WT, roX1, roX2, roX1roX2 mutants in D. melanogaster

(Submitter supplied) Study of single and double mutants of the two roX RNAs in D. melanogaster
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17275
13 Samples
Download data: TXT, XLSX
Series
Accession:
GSE115779
ID:
200115779
10.

Expansion of GA dinucleotide repeats increases the density of CLAMP binding sites on the X-chromosome to promote Drosophila dosage compensation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster; Drosophila miranda
Type:
Genome binding/occupancy profiling by high throughput sequencing; Genome binding/occupancy profiling by array
Platforms:
GPL17275 GPL22022 GPL22023
10 Samples
Download data: BROADPEAK, TXT
Series
Accession:
GSE83444
ID:
200083444
11.

CLAMP Protein Binding Microarray (PBM) experiment

(Submitter supplied) To investigate the DNA binding specificity of the CLAMP protein, we have designed a custom PBM to interrogate the binding of CLAMP to DNA sequences extracted from the Drosophila melanogaster genome. Specific regions were extracted based on ChIP-seq data, motif occurence and proximity to gene transcription start sites.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by array
Platform:
GPL22023
2 Samples
Download data: TXT
Series
Accession:
GSE83442
ID:
200083442
12.

Expansion of GA dinucleotide repeats increases the density of CLAMP binding sites on the X-chromosome to promote Drosophila dosage compensation [ChIP-Seq]

(Submitter supplied) ChIP-seq was performed to compare binding the genome-wide binding profile of the CLAMP transcription factor in two different Drosophila species.
Organism:
Drosophila melanogaster; Drosophila miranda
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL22022 GPL17275
8 Samples
Download data: BROADPEAK
Series
Accession:
GSE83435
ID:
200083435
13.

Non-canonical compensation of zygotic X transcription in Drosophila melanogaster development revealed through single embryo RNA-Seq

(Submitter supplied) We sequenced mRNA from 24 single D. melanogaster embryos (12 male and 12 female) taken from 8 early embryonic timepoints to generate the first sex specific timecourse of gene expression in early Drosophila development
Organism:
Drosophila melanogaster
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9061
24 Samples
Download data: BEDGRAPH, CUFF, SAM
Series
Accession:
GSE25180
ID:
200025180
14.

Sex-dependent and -independent X-chromosome histone modifications in Drosophila melanogaster

(Submitter supplied) Drosophila X chromosomes are subject to dosage compensation in males and are known to have a specialized chromatin structure in the male soma. We are interested in how specific chromatin structure change contributes to X chromosome hyperactivity and dosage compensation. We have conducted a global analysis of localize two dosage compensation complex dependent histone marks H4AcK16 and H3PS10 and one dosage compensation complex independent histone mark H3diMeK4 in the genome, especially on X chromosome by ChIP-chip approach in both male and female adult flies. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by array; Other
Platforms:
GPL20 GPL9058
17 Samples
Download data: GPR, TXT
15.

Global analysis of X chromosome dosage compensation

(Submitter supplied) We have conducted a global analysis of somatic dosage compensation and also asked if germ cell dosage compensate by microarray analysis of gene expression in wild-type tissues. To obviate the confounding effects of scatter and especially the skewed genomic distributions of genes with sex-biased expression in both the soma and germline [there are fewer X chromosome genes with male-biased expression], we used mutations that transform sexual identity. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Platform:
GPL20
27 Samples
Download data
Series
Accession:
GSE2119
ID:
200002119
16.

Sequence-specific targeting of dosage compensation in Drosophila favors an active chromatin context

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL5636 GPL1322
14 Samples
Download data: CEL, PAIR, TXT
Series
Accession:
GSE34859
ID:
200034859
17.

Sequence-specific targeting of dosage compensation in Drosophila favors an active chromatin context (mRNA)

(Submitter supplied) The Drosophila MSL complex mediates dosage compensation by increasing transcription of the single X chromosome in males approximately two-fold. This is accomplished through recognition of the X chromosome and subsequent acetylation of histone H4K16 on X-linked genes. Initial binding to the X is thought to occur at a subset of sites. However, the consensus sequence motif of entry sites (“MSL recognition element” or MRE) is only slightly enriched on the X (~2 fold), and only a fraction of them is utilized by the MSL complex. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Platform:
GPL1322
8 Samples
Download data: CEL
Series
Accession:
GSE34858
ID:
200034858
18.

Sequence-specific targeting of dosage compensation in Drosophila favors an active chromatin context (ChIP-chip)

(Submitter supplied) The Drosophila MSL complex mediates dosage compensation by increasing transcription of the single X chromosome in males approximately two-fold. This is accomplished through recognition of the X chromosome and subsequent acetylation of histone H4K16 on X-linked genes. Initial binding to the X is thought to occur at a subset of sites. However, the consensus sequence motif of entry sites (“MSL recognition element” or MRE) is only slightly enriched on the X (~2 fold), and only a fraction of them is utilized by the MSL complex. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL5636
6 Samples
Download data: PAIR, TXT
Series
Accession:
GSE34857
ID:
200034857
19.

Synergistic interactions between CLAMP and MSL complex facilitate Drosophila dosage compensation

(Submitter supplied) ChIP-seq and mRNA-seq experiments were performed to understand the role of the CLAMP protein in dosage compensation
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL13304
15 Samples
Download data: RPKM, WIG
Series
Accession:
GSE39271
ID:
200039271
20.

Sex-biased gene expression

(Submitter supplied) Investigatation into how genes with sex-differential expression profiles are distributed among the chromosomes in Drosophila. Assayed the expression of 14,142 predicted transcripts in competitive hybridizations and found a dramatic underrepresentation of X-chromosome genes showing high relative expression in male. This is the first report of sex-biased expression of the full (predicted) genome. Findings indicate that there is significant sex-biased expression, especially in gonads. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Platform:
GPL20
46 Samples
Download data
Series
Accession:
GSE442
ID:
200000442
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