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Series GSE46833 Query DataSets for GSE46833
Status Public on Jun 01, 2013
Title De novo mutations in the genome organizer CTCF cause Intellectual Disability
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s) 23746550
Submission date May 10, 2013
Last update date Jun 14, 2022
Contact name Jo Huiqing Zhou
E-mail(s) jo.zhou@radboudumc.nl
Organization name Radboud University
Street address Geert Grooteplein 26/18
City Nijmegen
ZIP/Postal code 6525GA
Country Netherlands
 
Platforms (2)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
GPL13393 AB SOLiD 4 System (Homo sapiens)
Samples (12)
GSM1138974 P1 RNA-Seq
GSM1138975 P2 RNA-Seq
GSM1138976 P3 RNA-Seq
This SuperSeries is composed of the following SubSeries:
GSE46831 De novo mutations in the genome organizer CTCF cause Intellectual Disability (RNA-Seq)
GSE46832 De novo mutations in the genome organizer CTCF cause Intellectual Disability (ChIP-Seq)
Relations
BioProject PRJNA202441

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
GSE46833_RAW.tar 890.0 Kb (http)(custom) TAR (of BED, XLS)
SRA Run SelectorHelp

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