HipSci___RNAseq___Rare_BBS
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 perform RNAseq on iPS cells generated from skin biopsies or blood samples from rare disease patients diagnosed with Bardet-Biedl syndrome This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/
- Type: Transcriptome Analysis
- Archiver: European Genome-Phenome Archive (EGA)
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 |
|---|---|---|---|
| EGAD00001001952 | Illumina HiSeq 2000 | 2 | |
| EGAD00001001954 | Illumina HiSeq 2000 | 3 | |
| EGAD00001003181 | Illumina HiSeq 2000 Illumina HiSeq 2500 | 3 | |
| EGAD00001003531 | Illumina HiSeq 2000 Illumina HiSeq 2500 | 3 |
| Publications | Citations |
|---|---|
|
Optimizing expression quantitative trait locus mapping workflows for single-cell studies.
Genome Biol 22: 2021 188 |
43 |