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Status |
Public on Sep 08, 2017 |
Title |
small RNAs produced by Dicer-2 [DHelicase] in vitro |
Sample type |
SRA |
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Source name |
104 bp dsRNA
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Organism |
synthetic construct |
Characteristics |
proteins: Dicer-2[DHelicase] sample type: in vitro
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Extracted molecule |
other |
Extraction protocol |
Female fly heads were hand-dissected and RNAs were prepared using miRVana. Libraries were prepared as previously described (Fukunaga et al, 2014 and Han et al, 2015).
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Library strategy |
ncRNA-Seq |
Library source |
transcriptomic |
Library selection |
size fractionation |
Instrument model |
Illumina HiSeq 4000 |
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Description |
small RNAs produced from 104 bp dsRNA in vitro The sequences of strands 1 and 2 of the 104 bp dsRNAs are: 5'-GGGCCACAAGUUCAGCGUGUCCGGCGAGGGCGAGGGCGAUGCCACCUACGGCAAGCUGACCCUGAAGUUCAUCUGCACCACCGGCAAGCUGCCCGUGCCCUGGCCC-3' and 5'-GCCAGGGCACGGGCAGCUUGCCGGUGGUGCAGAUGAACUUCAGGGUCAGCUUGCCGUAGGUGGCAUCGCCCUCGCCCUCGCCGGACACGCUGAACUUGUGGCCCAA-3'. These two strands make 104 bp dsRNA with 3' 2-nt overhang at both ends.
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Data processing |
Basecalls performed using bcl2fastq version 2.16 Sequenced reads were trimmed for adaptor sequence. Genome_build: dm3 Supplementary_files_format_and_content: [.txt] Tab-delimited text file. Length of the read, Number of the read, Sequence of the read.
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Submission date |
Sep 14, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Ryuya Fukunaga |
E-mail(s) |
fukunaga@jhmi.edu
|
Phone |
4109553790
|
Organization name |
Johns Hopkins University School of Medicine
|
Department |
Department of Biological Chemistry
|
Street address |
725 N. Wolfe St. 521A Physiology Bldg
|
City |
BALTIMORE |
State/province |
MD |
ZIP/Postal code |
21205 |
Country |
USA |
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Platform ID |
GPL21616 |
Series (1) |
GSE94803 |
small RNAs produced in the mutant Dicer-2 transgenic flies |
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Relations |
BioSample |
SAMN05771107 |
SRA |
SRX2606824 |