Aleixo Muise Data Access Committee

Request Access

Dataset ID	Description	Technology	Samples
EGAD00001004485	This project focused on identifying rare coding variation that substantially increases risk of VEOIBD by exome sequencing of VEOIBD patients and some of their family members. Here you can find BAM files from an affected proband (P2) and his unaffected parents. In this study ALPI mutations were identified as a likely cause of the disease.	Illumina HiSeq 2500	3