Type 1 Diabetes Genetics Consortium (T1DGC) was formed to address issues of limited sample size and consistency of phenotyping that had limited genetic investigations on risk of type 1 diabetes (T1D).
Primary uveal melanomas show multiple chromosomal aberrations. To identify genome variation in six human primary uveal melanomas, genome wide copy number variation (CNV) analyses were carried out in h
The data and code used in the manuscript entitled "Identification and Validation of a Gene-based Signature Reveals SLC25A10 as a Novel Prognostic Indicator for Patients with Ovarian Cancer".