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
HipSci - Usher Syndrome - Expression Array - July 2017
Illumina 1

Who archives the data?

There are no publications available