Whole exome sequencing of rare autoimmune related phenotypes
|Study ID||Alternative Stable ID||Type|
Study Datasets 1 dataset.
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We aim to whole-exome sequence DNA samples from 75 individuals with severe forms of Inflammatory Bowel Disease and related autoimmune diseases to identify the rare, highly penetrant, variants that we believe underlie these phenotypes. Case samples will be obtained from both new and existing (UK IBD Genetics Consortium) collaborators to ensure only the most extreme cases are sequenced.
|Illumina HiSeq 2000||4|