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Series GSE153101 Query DataSets for GSE153101
Status Public on Feb 17, 2021
Title Gene therapy of dominant CRX-Leber congenital amaurosis using patient retinal organoids
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s) 33513359
Submission date Jun 23, 2020
Last update date Nov 09, 2023
Contact name Zachary A Batz
Organization name NIH
Department NEI
Lab NNRL
Street address 6 Center Dr Bldg 6, Rm 303
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platforms (2)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (43)
GSM4630032 NEI002-I138fs-Control-D125-1
GSM4630033 NEI002-I138fs-Control-D125-2
GSM4630034 NEI002-I138fs-Control-D125-3
This SuperSeries is composed of the following SubSeries:
GSE152939 Gene therapy of dominant CRX-Leber congenital amaurosis using patient retinal organoids I
GSE153099 Gene therapy of dominant CRX-Leber congenital amaurosis using patient retinal organoids II
Relations
BioProject PRJNA641425

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
GSE153101_RAW.tar 381.4 Mb (http)(custom) TAR (of H5)
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