ID
46001
Descripción
Principal Investigator: Levi A. Garraway, MD, PhD, 1. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA 2. Broad Institute of Harvard and MIT, Cambridge, MA, USA MeSH: Male Germ Cell Tumor https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000923 We performed comprehensive molecular profiling of germ cell tumors, including whole exome sequencing and transcriptome sequencing, derived from patient samples. This project additionally explores mechanisms of chemosensivity in these patients, as well as mechanisms of tumor evolution in the context of treatment.
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Versiones (1)
- 18/4/24 18/4/24 - Madita Rudolph
Titular de derechos de autor
Levi A. Garraway, MD, PhD, 1. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA 2. Broad Institute of Harvard and MIT, Cambridge, MA, USA
Subido en
18 de abril de 2024
DOI
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Licencia
Creative Commons BY 4.0
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dbGaP phs000923 Molecular Characterization of Germ Cell Tumors
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent data table contains subject IDs and consent information.
- The subject sample mapping data table contains a mapping of study subject IDs to sample IDs. dbGaP samples are defined as the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample use.
- This subject phenotype table includes subject IDs and gender of participant.
- This sample attributes table includes sample IDs, sample type, and analyte type.
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Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent data table contains subject IDs and consent information.
- The subject sample mapping data table contains a mapping of study subject IDs to sample IDs. dbGaP samples are defined as the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample use.
- This subject phenotype table includes subject IDs and gender of participant.
- This sample attributes table includes sample IDs, sample type, and analyte type.
C0680251 (UMLS CUI [1,2])
C0475358 (UMLS CUI [1,2])
C3845275 (UMLS CUI [1,3])