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Identifying and understanding changes in cancer genomes is essential for the development of targeted therapeutics. Here we analyse systematically more than 70 pairs of primary human colon tumours by applying next-generation sequencing to characterize their exomes, transcriptomes and copy-number alte...

Hepatitis B virus (HBV) infection is a major risk factor for hepatocellular carcinoma (HCC). In this study we sequenced the whole genome (~80X) and transcriptome of tumor and non-tumor samples from four HCC patients and identified over two hundred HBV integration sites. We found significant clona...

Colon matched tumour samples
Colon tumour samples
Exome capture sequencing of colon tumor/normal pairs
RNA sequencing of colon tumor/normal sample pairs
Whole genome sequencing of colon samples
Data Access Committee EGAC00001000055
Lung cancer is a highly heterogeneous disease in terms of both underlying genetic lesions and response to therapeutic treatments. We performed deep whole genome sequencing and transcriptome sequencing on 19 lung cancer cell lines and 3 lung tumor/normal pairs (provisional dbGaP accession number; phs...
ORGANISM(S): Homo sapiens 
Whole genome sequencing of SCLC tumor/normal samples
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