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Series GSE214692 Query DataSets for GSE214692
Status Public on May 05, 2024
Title Dissecting developmental disorders caused by CTCF mutation at R567
Organisms Homo sapiens; Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Other
Expression profiling by high throughput sequencing
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
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Submission date Oct 03, 2022
Last update date May 06, 2024
Contact name gongcheng Hu
Organization name Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences
Street address 190 Kai Yuan Avenue, Science Park, Guangzhou, China
City guangzhou
State/province guangdong
ZIP/Postal code 510530
Country China
 
Platforms (4)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
GPL29480 DNBSEQ-T7 (Homo sapiens)
Samples (71)
GSM6614265 CTCF_ChIP_brain_wt
GSM6614266 CTCF_ChIP_brain_homo
GSM6614267 CTCF_ChIP_heart_wt
This SuperSeries is composed of the following SubSeries:
GSE214686 Dissecting developmental disorders caused by CTCF mutation at R567 [ChIP-seq]
GSE214687 Dissecting developmental disorders caused by CTCF mutation at R567 [Hi-C]
GSE214688 Dissecting developmental disorders caused by CTCF mutation at R567 [4C]
Relations
BioProject PRJNA886671

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
GSE214692_RAW.tar 7.9 Gb (http)(custom) TAR (of BW, CSV, HIC, MTX, NARROWPEAK, TSV)
SRA Run SelectorHelp

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