HipSci Illumina Methylation analysis - Usher syndrome and congenital eye defects

The HipSci project brings together diverse constituents in genomics, proteomics, cell biology and clinical genetics to create a UK national iPS cell resource and use it to carry out cellular genetic studies. In this sub-study we performed Methylation analysis using the Infinium Methylation BeadChip on iPS cells generated from skin biopsies or blood samples from rare disease patients diagnosed with Usher syndrome and congenital eye defects.

• Type: Other
• Archive: European Genome-phenome Archive (EGA)