|
Status |
Public on Jan 11, 2022 |
Title |
Germline Variant in *Ctcf* Links Mental Retardation to Wilms Tumor Predisposition |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by genome tiling array Genome variation profiling by SNP array SNP genotyping by SNP array Genome variation profiling by high throughput sequencing
|
Summary |
This SuperSeries is composed of the SubSeries listed below.
|
|
|
Overall design |
Refer to individual Series
|
|
|
Citation(s) |
35459888 |
|
Submission date |
Jan 07, 2022 |
Last update date |
Apr 27, 2022 |
Contact name |
Jaime Font de Mora Sain |
E-mail(s) |
jaime.fontdemora@gmail.com
|
Phone |
+34961246646
|
Organization name |
Instituto de Investigación Sanitaria La Fe
|
Department |
Oncology
|
Lab |
Laboratory of Cellular and Molecular Biology
|
Street address |
Avenida Fernando Abril Martorell, 106
|
City |
Valencia |
State/province |
Valencia |
ZIP/Postal code |
46026 |
Country |
Spain |
|
|
Platforms (2) |
GPL16131 |
[CytoScanHD_Array] Affymetrix CytoScan HD Array |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
|
Samples (3) |
|
This SuperSeries is composed of the following SubSeries: |
GSE193017 |
SNP array data for Wilms Tumor harboring de novo germline mutation in CTCF |
GSE193233 |
Germline Variant in Ctcf Links Mental Retardation to Wilms Tumor Predisposition |
|
Relations |
BioProject |
PRJNA795462 |