|
Status |
Public on Jun 11, 2014 |
Title |
X. tropicalis brain small RNAs |
Sample type |
SRA |
|
|
Source name |
brain
|
Organism |
Xenopus tropicalis |
Characteristics |
Sex: Male individual: M2 tissue type: brain
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted from 20-30 mg of tissue, using the QIAgen miRNeasy mini kit according to the manufacturer's instructions. The RNA quality was checked using a Fragment Analyzer. 2ug of total RNA were used to prepare small RNA libraries: after a purification of the small RNA on a 15% TBU acrylamide gel, the libraries were generated using the Illumina TruSeq(R) Small RNA Sample Prep Kit and the quality assessed using a Fragment Analyzer.
|
|
|
Library strategy |
miRNA-Seq |
Library source |
transcriptomic |
Library selection |
size fractionation |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
small RNA
|
Data processing |
There are no processed data files associated with this submission. This is because the data were only used to test presence/absence of 15 transcripts that had been identified based on published datasets. We did not run any genome-wide expression analysis or similar.
|
|
|
Submission date |
Apr 10, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Maria Warnefors |
Organization name |
University of Heidelberg
|
Street address |
Center for Molecular Biology of Heidelberg University (ZMBH)
|
City |
Heidelberg |
ZIP/Postal code |
69120 |
Country |
Germany |
|
|
Platform ID |
GPL18470 |
Series (1) |
GSE56680 |
MicroRNA editing in Xenopus tropicalis |
|
Relations |
BioSample |
SAMN02725059 |
SRA |
SRX514968 |