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Series GSE100943 Query DataSets for GSE100943
Status Public on Aug 10, 2017
Title Microsatellite expansion RNA visualization, elimination, and reversal of molecular pathology by RNA-targeting Cas9
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary In this Study, we used RNA-targeting Cas9 (RCas9) to reverse characteristic Myotonic Dystrophy (DM1) cellular phenotypes such as elimination of RNA foci, MBNL relocalization, and reversal of transcriptome-wide splicing.
 
Overall design We performed RNA-seq for control and myotonic dystrophy (DM1) myoblasts and myotubes with various treatments including lentivirus mediated expression of either non-targeting (NT) or CTG-targeting (CTG) single guide RNA (sgRNA) and PIN-dCas9.Lentivirus mediated GFP expression was used as control.
 
Contributor(s) Batra R, Yeo G
Citation(s) 28803727
Submission date Jul 07, 2017
Last update date May 15, 2019
Contact name Ranjan Batra
E-mail(s) ranjanbatra9@yahoo.com
Phone 352-222-9209
Organization name University of California San Diego
Department Cellular and Molecular Medicine
Lab Yeo Lab
Street address 2880 Torrey Pines Scenic Drive
City La Jolla
State/province California
ZIP/Postal code 92037
Country USA
 
Platforms (1)
GPL20301 Illumina HiSeq 4000 (Homo sapiens)
Samples (9)
GSM2696922 myoblast_Control-Non targeting
GSM2696923 myoblast_Control-CTG targeting
GSM2696924 myoblast_Myotonic Dystriphy type I (DM1) GFP
Relations
BioProject PRJNA393468
SRA SRP111361

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE100943_RPKM_myo.txt.gz 1000.9 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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