Study
HipSci HumanHT 12 Expression BeadChip analysis - Usher syndrome and congenital eye defects
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001002023 | Other |
Study Description
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 Expression analysis using the Illumina HumanHT -12 Expression BeadChip on iPS cells generated from skin biopsies or blood samples from rare disease patients diagnosed with Usher syndrome and congenital eye defects.
Study Datasets 1 dataset.
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD00010001374 |
HipSci - Usher Syndrome - Expression Array - July 2017
|
Illumina | 1 |
Who archives the data?
