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Series GSE244520 Query DataSets for GSE244520
Status Public on Jan 22, 2024
Title DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Methylation profiling by high throughput sequencing
Expression profiling by high throughput sequencing
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s) 38291337
Submission date Oct 03, 2023
Last update date Feb 06, 2024
Contact name Duncan Sproul
Organization name University of Edinburgh
Department MRC Human Genetics Unit
Street address Crewe Road South
City Edinburgh
State/province Mid Lothian
ZIP/Postal code EH4 2XU
Country United Kingdom
 
Platforms (3)
GPL21697 NextSeq 550 (Homo sapiens)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
GPL30173 NextSeq 2000 (Homo sapiens)
Samples (80)
GSM7818542 HCT116_exp_1_WGBS
GSM7818543 DNMT3B_KO_exp_1_WGBS
GSM7818544 DNMT3B_KO_DNMT3B_exp_1_WGBS
This SuperSeries is composed of the following SubSeries:
GSE244516 DNMT3B PWWP mutations cause hypermethylation of heterochromatin (T7-DNMT3B ChIP-seq)
GSE244517 DNMT3B PWWP mutations cause hypermethylation of heterochromatin (WGBS)
GSE244518 DNMT3B PWWP mutations cause hypermethylation of heterochromatin (RNA-seq)
Relations
BioProject PRJNA1023399

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
GSE244520_RAW.tar 2.6 Gb (http)(custom) TAR (of BIGWIG, COV, TXT)
SRA Run SelectorHelp
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