NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE33772 Query DataSets for GSE33772
Status Public on Feb 10, 2012
Title Circular RNAs are the predominant transcript isoform from hundreds of human genes in diverse cell types
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Most human pre-mRNAs are spliced into linear molecules that retain the exon order defined by the genomic sequence. By deep sequencing of RNA from a variety of normal and malignant human cells, we found RNA transcripts from many human genes in which the exons were arranged in a non-canonical order. Statistical estimates and biochemical assays provided strong evidence that a substantial fraction of the spliced transcripts from hundreds of genes are circular RNAs. Our results suggest that a non-canonical mode of RNA splicing, resulting in a circular RNA isoform, is a widespread and perhaps general feature of the gene expression program in human cells.
 
Overall design 3 samples of non-malignant primary human leukocytes, one replicate each
 
Contributor(s) Salzman J
Citation(s) 22319583
Submission date Nov 17, 2011
Last update date May 15, 2019
Contact name Julia Salzman
E-mail(s) julia.salzman@gmail.com
Organization name Stanford University
Street address 279 West Campus Drive, MC: 5307
City Stanford
ZIP/Postal code 94305
Country USA
 
Platforms (1)
GPL9115 Illumina Genome Analyzer II (Homo sapiens)
Samples (3)
GSM835231 CD19
GSM835232 CD34
GSM835233 neutrophils
Relations
SRA SRP009373
BioProject PRJNA148385

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE33772_RAW.tar 2.0 Gb (http)(custom) TAR (of BOWTIE)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap