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).
This FAIRsharing record describes: Clinical information about tumor samples and microarray data, with emphasis on array comparative genomic hybridization (aCGH) and data mining of gene copy number ch
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
Secondary structure in the H19 transcript, which is altered through a SNP in DCM patients, is an attractive target for future studies investigating the molecular mechanism by which H19 contributes to
