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Whole genome sequencing of SCLC tumor/normal samples
SCLC matched normal genotypes
SCLC tumor genotypes
Exome capture sequencing of SCLC tumor/normal pairs and cell lines
RNA sequencing of SCLC tumor/normal sample pairs and cell lines
Exome capture, RNA-Seq, whole genome sequencing of set of Small Cell Lung Cancer samples.

This study funded by the National Cancer Institute (NCI) involves conducting a genome-wide association study of common genetic variants to identify markers of susceptibility to bladder cancer.

This bladder GWAS has led to the discovery of three novel regions in the genome associated with...

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