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Whole Genome and Exon Capture Sequencing of Bladder Cancers

UID: 11285

Author(s): Solit, David*, Taylor, Barry Stephen* * MSK affiliated

Description
From the dbGaP study description:

"One primary bladder cancer and paired peripheral blood sample were subjected to whole genome sequencing on an Illumina HiSeq 2000 platform. This technology was utilized to investigate the genetic basis of a durable remission of metastatic bladder cancer in a patient treated with everolimus, a drug that inhibits the mTOR (mammalian target of rapamycin) signaling pathway. Among the somatic mutations found was a loss-of-function mutation in TSC1 (Tuberous Sclerosis Complex 1), a regulator of mTOR pathway activation. Targeted sequencing using an exon capture and sequencing assay was performed on 13 tumors derived from patients on the same everolimus trial as the index patient and the sequencing data from these tumors is included. TSC1 mutation status was correlated with response to everolimus. The index patient responder tumor and peripheral blood DNA were also subjected to exon capture and sequencing."
Subject of Study
Subject(s)
Access via dbGaP


Accession #: phs000535.v1.p1

Access Restrictions
Application Required
Access Instructions
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Publicly available data such as data dictionaries, variable summaries, documents and truncated analysis are available the public download site FTP link.
Associated Publications
Data Type
Equipment Used
Illumina HiSeq 2000
Dataset Format(s)
PDF, TAR, gzip, TXT
Dataset Size
115.88 KB
Data Catalog Record Updated
2024-06-19