Here We have performed sequencing of 412 cancer gene panel in 5 PDAC ad 3 PAC tumour blood paired sample. We used Hiseq2500 platform to generate 100 bp pair end reads. We have identified total 48 soma
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
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).
