PRAD-CA, DCC Release 26 : This dataset contains fastq files with Whole genome sequencing data for the CPC-Gene Project. Data from each sample was generated using multiple whole genome libraries and se
Whole-genome sequencing reads from the LNCaP human prostate cancer cell line were used to generate a de novo assembly with SGA v0.10.15. Please see https://github.com/sciseim/PCaWGS for assoc
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
