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Links from GEO DataSets

Items: 20

1.

A coordinated regulatory network of ApiAP2 transcription factors involved in heterochromatic gene expression during Plasmodium falciparum blood-stage development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
192 Samples
Download data: BED, BW
Series
Accession:
GSE184659
ID:
200184659
2.

A coordinated regulatory network of ApiAP2 transcription factors involved in heterochromatic gene expression during Plasmodium falciparum blood-stage development [ChIP-Seq]

(Submitter supplied) Genome-wide occupancy of sixteen PfApiAP2 transcription factors and PfHP1 throughout the intraerythrocytic cycle
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
144 Samples
Download data: BED, BW
Series
Accession:
GSE184658
ID:
200184658
3.

A coordinated regulatory network of ApiAP2 transcription factors involved in heterochromatic gene expression during Plasmodium falciparum blood-stage development [RNA-Seq]

(Submitter supplied) Effects of PfApiAP2 knockouts on gene expression in the intraerythrocytic cycle
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26835
48 Samples
Download data: CSV
Series
Accession:
GSE184645
ID:
200184645
4.

Transgenic Plasmodium falciparum parasites line 3D7/DDGFP-PfAP2-HC: transcriptional differences between 3D7/DDGFP-PfAP2-HC control parasites (cultured in presence of Shield-1; ON) vs PfAP2-HC-depleted parasites (cultured in absence of Shield-1; OFF)

(Submitter supplied) Transcriptional profiling of transgenic P. falciparum asexual blood stage parasites of the transgenic strain 3D7/DDGFP-PfAP2-HC at five time points during intra-erythrocytic parasite development. The DD (FKBP destabilisation domain) allows for the conditional expression of fusion proteins: DD fusion proteins are rapidly degraded or stably expressed in absence or presence of the stabilising ligand Shield-1, respectively (Banaszynski LA, Chen LC, Maynard-Smith LA, Ooi AG, Wandless TJ. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
10 Samples
Download data: GPR
Series
Accession:
GSE159061
ID:
200159061
5.

PfAP2-HC, an unusual, heterochromatin-associated ApiAP2 factor of Plasmodium falciparum

(Submitter supplied) In this study we have investigated PfAP2-HC (PF3D7_1456000), a protein that was identified by co-immunoprecipitation with PfHP1 coupled with liquid chromatography-tandem mass spectrometry. PfAP2-HC belongs to the ApiAP2 family, the main transcription factor family in Apicomplexan parasites. We have confirmed that AP2-HC colocalises with HP1 with the use of immunofluorescence assays and chromatin immunoprecipitation-sequencing. more...
Organism:
Plasmodium falciparum 3D7
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25935
17 Samples
Download data: BEDGRAPH
Series
Accession:
GSE154840
ID:
200154840
6.

PfAP2-I-GFP anti-GFP and anti-IgG ChIP-seq

(Submitter supplied) To determine the genome-wide occupancy of the Plasmodium falciparum transcriptional regulator of invasion PfAP2-I (PfDd2_100013100/PF3D7_1007700), we used chromatin immunoprecipitation coupled with next-generation sequencing (ChIP-seq). Synchronized, schizont stage, 40 hours post-invasion, cultures of parasites expressing the AP2-I-GFP fusion protein were treated with formaldehyde to crosslink proteins to DNA and harvested. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21078
9 Samples
Download data: BEDGRAPH
Series
Accession:
GSE80293
ID:
200080293
7.

Rrp6-mediated heterochromatin surveillance secures antigenic variation and sexual commitment of human malaria parasites

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Other; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL26835 GPL26836
111 Samples
Download data: BW, HIC
Series
Accession:
GSE133241
ID:
200133241
8.

HIC_seq data for Rrp6 project analysis in malaria (Plasmodium falciparum)

(Submitter supplied) We performed Hi-C assay to address the interaction of central var genes in ruf6-var pairs,subtelomeric upsA-subtype var genes and other HP1-associated genes
Organism:
Plasmodium falciparum
Type:
Other
Platform:
GPL26835
2 Samples
Download data: HIC
Series
Accession:
GSE133240
ID:
200133240
9.

ChIRP_seq data for Rrp6 project analysis in malaria (Plasmodium falciparum)

(Submitter supplied) We adopted the technique of Chromatin Isolate by RNA Purification combined with high-throughput sequencing (ChIRP-seq) to gain mechanistic insight into the transcriptionally regulatory role of the trans-acting RUF6 ncRNA in detail
Organism:
Plasmodium falciparum
Type:
Other
Platforms:
GPL26835 GPL26836
9 Samples
Download data: BW
Series
Accession:
GSE133239
ID:
200133239
10.

ChIP_seq data for Rrp6 project analysis in malaria (Plasmodium falciparum)

(Submitter supplied) We carried out chromatin immunoprecipitation followed by deep sequencing (ChIP-seq) to explore the difference of the genome-wide dynamics of histone modifications and HP1 in PfRrp6-DD-1C line.
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
23 Samples
Download data: BW
Series
Accession:
GSE133238
ID:
200133238
11.

RIP_seq data for Rrp6 project analysis in malaria (Plasmodium falciparum)

(Submitter supplied) We carried out RNA Immunoprecipitation followed by deep sequencing (RIP-seq) to explore the difference of direct target substrates of PfRrp6 and RNA exosome core
Organism:
Plasmodium falciparum
Type:
Other
Platform:
GPL26835
20 Samples
Download data: XLSX
Series
Accession:
GSE133237
ID:
200133237
12.

RNA_seq data for Rrp6 project analysis in malaria (Plasmodium falciparum)

(Submitter supplied) We carried out strand-specific RNA-seq libraries followed by deep sequencing (RNA-seq) to explore the transcriptional profile of the PfRrp6-DD-1C,PfRrp6-DD-1B,PfRrp6-DD-4C,WT 3D7-G7, WT NF54 and PfMaf1-OE lines.
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26835
57 Samples
Download data: XLSX
Series
Accession:
GSE133236
ID:
200133236
13.

The PfAP2-G2 transcription factor is a critical regulator of gametocyte maturation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
44 Samples
Download data: TXT
Series
Accession:
GSE160937
ID:
200160937
14.

Plasmodium falciparum PfAP2-G2 KO gametocyte microarray timecourse

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human to the mosquito host. Preventing gametocyte commitment and development would block parasite transmission, but the underlying molecular mechanisms behind these processes remain poorly understood. Here, we report that the ApiAP2 transcription factor, PfAP2-G2 (PF3D7_1408200) plays a critical role in the maturation of Plasmodium falciparum gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
28 Samples
Download data: TXT
Series
Accession:
GSE160924
ID:
200160924
15.

Plasmodium falciparum PfAP2-G2 KO asexual microarray timecourse

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human to the mosquito host. Preventing gametocyte commitment and development would block parasite transmission, but the underlying molecular mechanisms behind these processes remain poorly understood. Here, we report that the ApiAP2 transcription factor, PfAP2-G2 (PF3D7_1408200) plays a critical role in the maturation of Plasmodium falciparum gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
16 Samples
Download data: TXT
Series
Accession:
GSE160923
ID:
200160923
16.

ChIP-seq on PfAP2-G2 in trophozoite and gametocyte stages of parasites.

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human host to mosquitos, where sexual fertilization occurs to complete the lifecycle. Although preventing gametocyte development would block parasite transmission, the molecular mechanisms underlying sexual commitment and gametocyte maturation are still relatively unknown. Previous studies identified an ApiAP2 protein, AP2-G2, which plays a critical role in gametocyte maturation in rodent malaria parasite Plasmodium berghei by acting as the repressor of asexual stage genes in gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21298
10 Samples
Download data: BIGWIG
Series
Accession:
GSE157753
ID:
200157753
17.

Comparative profiling of the heterochromatin landscape in different life cycle stages, strains and species of malaria parasites

(Submitter supplied) Heterochromatin is a tightly packaged form of DNA that leads to permanent or temporal gene silencing. In P. falciparum heterochromatin is formed after trimethylation of lysine 9 on histone H3 and consequent binding of heterochromatin protein 1 (HP1). Genome-wide profiling studies established that in P. falciparum blood stage schizonts heterochromatin is formed at subtelomeres and some intra-chromosomal islands. more...
Organism:
Plasmodium vivax; Plasmodium falciparum; Plasmodium knowlesi; Plasmodium berghei; Plasmodium chabaudi; Plasmodium yoelii
Type:
Genome binding/occupancy profiling by high throughput sequencing
6 related Platforms
26 Samples
Download data: BEDGRAPH
Series
Accession:
GSE102695
ID:
200102695
18.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [WGS-Seq]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome variation profiling by high throughput sequencing
Platform:
GPL26835
4 Samples
Download data: XLSX
Series
Accession:
GSE175931
ID:
200175931
19.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [ChIP-Seq HM]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
12 Samples
Download data: BW
Series
Accession:
GSE157709
ID:
200157709
20.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5)

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
117 Samples
Download data: BW
Series
Accession:
GSE149774
ID:
200149774
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