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Links from GEO DataSets

Items: 5

1.

Non-canonical crRNAs derived from host transcripts enable multiplexable RNA detection by Cas9 [RIP-seq]

(Submitter supplied) RIP-seq analysis to identify CjCas9 bound RNAs using co-immunoprecipitation and sequencing in CG84-21.
Organism:
Campylobacter jejuni subsp. jejuni CG8421
Type:
Other
Platform:
GPL29023
6 Samples
Download data: WIG
Series
Accession:
GSE156264
ID:
200156264
2.

Non-canonical crRNAs derived from host transcripts enable multiplexable RNA detection by Cas9

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Campylobacter jejuni subsp. jejuni CG8421
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL29024 GPL29023
10 Samples
Download data: WIG
Series
Accession:
GSE156266
ID:
200156266
3.

Non-canonical crRNAs derived from host transcripts enable multiplexable RNA detection by Cas9 [dRNA-seq]

(Submitter supplied) Differential RNA sequencing using terminator exonuclease (TEX) to identify processed versus unprocessed transcripts in Campylobacter jejuni strain CG84-21
Organism:
Campylobacter jejuni subsp. jejuni CG8421
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29024
4 Samples
Download data: WIG
Series
Accession:
GSE156265
ID:
200156265
4.

CRISPR RNA-dependent binding and cleavage of endogenous RNAs by the Campylobacter jejuni Cas9

(Submitter supplied) This study investigates the RNA targets and cleavage sites of endogenous Cas9 in the food-borne pathogen Campylobacter jejuni. Direct RNA binding targets of Cas9 in C. jejuni strain NCTC11168 were determined using RIP-seq. The Cleavage sites were then predicted in the RNA targets by comparing total transcriptome data from WT and deletion (cas9, crRNA3, tracrRNA, CRISPR-tracrRNA) strains. PAMs for the CjeCas9 were enriched using the PAM-SCANR platform, which operates through a GFP reporter gene. more...
Organism:
Escherichia coli K-12; Campylobacter jejuni
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL19974 GPL19168
13 Samples
Download data: TXT, WIG, XLSX
Series
Accession:
GSE106849
ID:
200106849
5.

Optimized RNA-targeting CRISPR/Cas13d technology outperforms shRNA in identifying functional circRNAs

(Submitter supplied) Circular RNAs (circRNAs) are widely expressed, but their functions remain largely unknown. To study circRNAs in a high-throughput manner, short hairpin RNA (shRNA) screens1 have recently been used to deplete circRNAs by targeting their unique back-splicing junction (BSJ) sites. Here, we report frequent discrepancies between shRNA-mediated circRNA knockdown efficiency and the corresponding biological effect, raising pressing concerns about the robustness of shRNA screening for circRNA functional characterization. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
4 related Platforms
22 Samples
Download data: TXT
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