Study
HipSci RNAseq Rare BBS
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001001318 | Transcriptome Analysis |
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 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/
Study Datasets 4 datasets.
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 |
HipSci - Bardet-Biedl Syndrome - RNA Sequencing - April 2015
|
Illumina HiSeq 2000 | 2 |
| EGAD00001001954 |
HipSci - Bardet-Biedl Syndrome - RNA Sequencing - January 2016
|
Illumina HiSeq 2000 | 3 |
| EGAD00001003181 |
HipSci - Bardet-Biedl Syndrome - RNA Sequencing - October 2016
|
Illumina HiSeq 2000,Illumina HiSeq 2500 | 3 |
| EGAD00001003531 |
HipSci - Bardet-Biedl Syndrome - RNA Sequencing - July 2017
|
Illumina HiSeq 2000,Illumina HiSeq 2500 | 3 |
Who archives the data?
