|
Status |
Public on Jun 30, 2015 |
Title |
dcl3_Apr1G |
Sample type |
SRA |
|
|
Source name |
10 day-old protonemata
|
Organism |
Physcomitrium patens |
Characteristics |
genotype: dcl3 tissue: protonemal tissue
|
Treatment protocol |
None
|
Growth protocol |
protonemal tissue was grown on cellophane-overlaid BCD media {Ashton, 1977} supplemented with 50mM ammonium tartarate under 16hr days, 8hr nights at 22ÂșC.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted with Tri-Reagent (Sigma) per the manufacturer's instructions small RNA-seq libraries for the Illumina HiSeq2500 were prepared using the Illumina TruSeq Small RNA protocol, as described by the manufacturer
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
size fractionation |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
FASTQ data were groomed by removal of 3' adapter sequences using ShortStack (version 1.1.0) with adapter sequence "ATCTCGTA". The right-most exact match to this sequence was inferred to be the 3' adapter junction, and was the site of trimming. Reads < 15 after trimming, and reads where the adapter was not found were discarded. Trimmed FASTQ data was counted to make a table giving the frequencies of each unique small RNA sequence in tab-delimited text format. Genome_build: n/a Supplementary_files_format_and_content: Processed data files are tab-delimited text files giving 1) Small RNA sequences, 2) Frequencies
|
|
|
Submission date |
Oct 18, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Michael J Axtell |
E-mail(s) |
[email protected]
|
Organization name |
Pennsylvania State University
|
Department |
Biology
|
Lab |
Axtell
|
Street address |
280 Mueller Lab
|
City |
University Park |
State/province |
PA |
ZIP/Postal code |
16802 |
Country |
USA |
|
|
Platform ID |
GPL17793 |
Series (1) |
GSE51419 |
small RNA-seq of Physcomitrella patens small RNA mutants |
|
Relations |
BioSample |
SAMN02377973 |
SRA |
SRX365400 |