|
Status |
Public on Jan 22, 2017 |
Title |
RNF125 mutated individual OGS009 |
Sample type |
genomic |
|
|
Source name |
RNF125 mutated individual
|
Organism |
Homo sapiens |
Characteristics |
gender: Male genotype: RNF125 mutation health state: Diseased donor
|
Extracted molecule |
genomic DNA |
Extraction protocol |
DNA extracted by Phenol:Chloroform:Isoamylalcohol (Sigma)
|
Label |
Cy3, Cy5
|
Label protocol |
Standard Illumina labelling protocol
|
|
|
Hybridization protocol |
Bisulphite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
|
Scan protocol |
Arrays were imaged using High Scan SQ using standard recommended Illumina scanner setting
|
Data processing |
Genome Studio V2011.2
|
|
|
Submission date |
Jan 23, 2014 |
Last update date |
Jan 22, 2017 |
Contact name |
Manel Esteller |
Organization name |
IDIBELL
|
Department |
PEBC
|
Lab |
Cancer Epigenetics
|
Street address |
Hospital Duran i Reynals Av. Gran Via s/n km, 2.7
|
City |
L'Hospitalet de Llobregat |
State/province |
Barcelona |
ZIP/Postal code |
08908 |
Country |
Spain |
|
|
Platform ID |
GPL13534 |
Series (1) |
GSE54335 |
A new syndrome of overgrowth, macrocephaly, hypoglycemia, enlarged ventricles, mild, and moderate intellectual disability and recurrent inflammatory disease is due to mutations in RNF125 |
|