|
Status |
Public on Mar 18, 2014 |
Title |
ddm1-2 [PARE-seq] |
Sample type |
SRA |
|
|
Source name |
mix-stage inflorescence
|
Organism |
Arabidopsis thaliana |
Characteristics |
tissue: mix-stage inflorescence genotype/variation: ddm1-2
|
Growth protocol |
Arabidopsis grown under standard long day growth conditions.
|
Extracted molecule |
total RNA |
Extraction protocol |
Mix-stage inflorescence (contain majority of unopened flower buds) were collected and flash frozen in liquid nitrogen. Total RNA was extracted by Tri reagent (Invitrogen) according to manufacturer's protocol. PARE: Degradome libraries (PARE) libraries were constructed as previously described (Zhai et al. 2013 PMID: 23810899). The libraries were sequenced on an Illumina HiSeq at the Delaware Biotechnology Institute (Newark, DE).
|
|
|
Library strategy |
ncRNA-Seq |
Library source |
transcriptomic |
Library selection |
size fractionation |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
Degradome analysis in Arabidopsis to validate microRNA prediction cleavage sites at transposons.
|
Data processing |
The adapter sequences were trimmed from raw sequence reads, and then the small RNA sequences were trimmed to the lengths between 18 and 34 nucleotides. Genome_build: Arabidopsis TAIR10 genome Supplementary_files_format_and_content: tag count file
|
|
|
Submission date |
Nov 13, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Kate M Creasey |
Organization name |
Cold Spring Harbor Laboratory
|
Department |
Plant Sciences
|
Street address |
1 Bungtown Road
|
City |
Cold Spring Harbor |
State/province |
NY |
ZIP/Postal code |
11724 |
Country |
USA |
|
|
Platform ID |
GPL13222 |
Series (2) |
GSE52342 |
miRNAs trigger widespread epigenetically-activated siRNAs from transposons in Arabidopsis [PARE-seq] |
GSE52952 |
miRNAs trigger widespread epigenetically-activated siRNAs from transposons in Arabidopsis |
|
Relations |
BioSample |
SAMN02422676 |
SRA |
SRX384363 |