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Sample GSM5861610 Query DataSets for GSM5861610
Status Public on Feb 17, 2022
Title tagassociations_benchmark
Sample type SRA
 
Source name plasmid vector
Organism synthetic construct
Characteristics cell line: NA
library: benchmark
molecule: plasmid
Treatment protocol Cells were electroporated by using NEON transfection system and recovered in culture medium for 24 hours.
Growth protocol 37C with 5% CO2 supplementation
Extracted molecule other
Extraction protocol Total RNA was purified by using Maxi RNeasy (QIAGEN) from homogenized cells. Then GFP mRNA was isolated by using biotinilated primers and magnetic beads followd by cDNA synthesis.
Libraries were initially amplified from cDNA or plasmid, and then secondarily amplified and added P5 and P7 tag sequences.
 
Library strategy OTHER
Library source transcriptomic
Library selection other
Instrument model Illumina MiSeq
 
Data processing Library strategy: MPRA
Sequences were processed through MPRAduo pipeline (https://github.com/tewhey-lab/MPRAduo).
Supplementary_files_format_and_content: Processed data files contain raw count tables for barcode tag.
 
Submission date Feb 04, 2022
Last update date Feb 17, 2022
Contact name Kousuke Mouri
E-mail(s) kousuke.mouri@jax.org
Organization name The Jackson Laboratory
Street address 600 Main Street
City Bar Harbor
State/province ME
ZIP/Postal code 04609
Country USA
 
Platform ID GPL17769
Series (1)
GSE196171 Whole genome functional characterization of RE1 silencers using a modified massively parallel reporter assay
Relations
BioSample SAMN25655149
SRA SRX14046719

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data not provided for this record

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