|
Status |
Public on Apr 05, 2012 |
Title |
Wild-type small RNAs Sample 1 |
Sample type |
SRA |
|
|
Source name |
Whole worm
|
Organism |
Caenorhabditis elegans |
Characteristics |
strain: Wild-type (N2) developmental stage: mixed stage tissue: Whole worm
|
Growth protocol |
Worms were grown on OP50 lawn at 20 degrees Celsius
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolating using TRIzol reagent (Invitrogen), small RNAs were isolated by gel purication and cDNA was prepared using the small RNA v1.5 illumina kit
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
size fractionation |
Instrument model |
Illumina Genome Analyzer II |
|
|
Description |
small RNA (18-30 nts) with 5' monophosphate
|
Data processing |
Sequence reads were obtained using the Illumina Genome Analyzer Pipeline version 1.6 (OLB 1.6, CASAVA 1.6.0)
Alingment: Sequnces were aligned to the genome (May 2008) using Novoalign, with an r-value of 0.2 and a q-value of 5. Sequences were filtered using the USeq. software package component NovoalignParser, using a posterior probability of 0.1. Output is a bed file for each chromosome, with separate files for plus and minus strands.
|
|
|
Submission date |
Apr 27, 2011 |
Last update date |
May 15, 2019 |
Contact name |
Michael Bryan Warf |
E-mail(s) |
warf@biochem.utah.edu
|
Phone |
801-585-3110
|
Organization name |
University of Utah
|
Department |
Biochemistry
|
Lab |
Brenda Bass
|
Street address |
15 N Medical Dr East, room 4800
|
City |
Salt Lake City |
State/province |
UT |
ZIP/Postal code |
84112 |
Country |
USA |
|
|
Platform ID |
GPL9269 |
Series (1) |
GSE28888 |
Effects of ADARs on small RNA processing pathways in C. elegans |
|
Relations |
Reanalyzed by |
GSE89765 |
SRA |
SRX059215 |
BioSample |
SAMN00261233 |