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?

There are no publications available