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Sample GSM5861614 Query DataSets for GSM5861614
Status Public on Feb 17, 2022
Title tagcounts_WGREST_SKNSH
Sample type SRA
 
Source name SK-N-SH
Organism Homo sapiens
Characteristics cell line: SK-N-SH
library: WGREST
molecule: GFP mRNA
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 total RNA
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 NovaSeq 6000
 
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 GPL24676
Series (1)
GSE196171 Whole genome functional characterization of RE1 silencers using a modified massively parallel reporter assay
Relations
BioSample SAMN25655145
SRA SRX14046723

Supplementary file Size Download File type/resource
GSM5861614_MPRAduo_counts_WGREST_SKNSH.txt.gz 6.8 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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