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Series GSE218691 Query DataSets for GSE218691
Status Public on Nov 30, 2023
Title Variants in ZFX Cause an X-linked Neurodevelopmental Disorder with Recurrent Facial Gestalt
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) 38325380
Submission date Nov 23, 2022
Last update date Feb 29, 2024
Contact name Peggy J Farnham
Organization name USC Keck School of Medicine
Department Biochemistry and Molecular Biology
Lab Farnham Lab
Street address 1450 Biggy St
City Los Angeles
State/province California
ZIP/Postal code 90089
Country USA
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (26)
GSM6754862 USC_RNA482, DKO, pCMV6, rep1
GSM6754863 USC_RNA483, DKO, pCMV6, rep2
GSM6754864 USC_RNA484, DKO, pCMV6, rep3
This SuperSeries is composed of the following SubSeries:
GSE218688 Variants in ZFX Cause an X-linked Neurodevelopmental Disorder with Recurrent Facial Gestalt
GSE218689 Variants in ZFX Cause an X-linked Neurodevelopmental Disorder with Recurrent Facial Gestalt
Relations
BioProject PRJNA904808

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
GSE218691_RAW.tar 13.7 Gb (http)(custom) TAR (of BW, NARROWPEAK)
SRA Run SelectorHelp

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