ID

45143

Description

Principal Investigator: Mark A. Rubin, MD, Weill Cornell Medical College, New York, NY, USA MeSH: Prostatic Neoplasms https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000330 Seven primary prostate cancers and their paired normal counterparts were DNA-sequenced on a massively parallel sequencing platform. This approach was taken to investigate the genomes for mutations and genomic alterations that would be undetectable by lower-resolution methods. As result, tumors containing chains of balanced rearrangements that occurred within or adjacent to known cancer genes were discovered.

Link

dbGaP study=phs000330

Keywords

  1. 10/8/22 10/8/22 - Adrian Schulz
  2. 10/12/22 10/12/22 - Adrian Schulz
  3. 10/12/22 10/12/22 - Adrian Schulz
Copyright Holder

Mark A. Rubin, MD, Weill Cornell Medical College, New York, NY, USA

Uploaded on

October 12, 2022

DOI

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License

Creative Commons BY 4.0

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dbGaP phs000330 The Genomic Complexity of Primary Human Prostate Cancer

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1512693
Prostate tissues collected post-robotic prostatectomy surgery and containing high-density tumor areas were used for this study. DNA samples in the study were extracted from tissue and blood, which were collected prior to the prostatectomy surgery.
Description

Elig.phs000330.v1.p1.1

Data type

boolean

Alias
UMLS CUI [1,1]
C3846158

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion and exclusion criteria
C0680251 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
Elig.phs000330.v1.p1.1
Item
Prostate tissues collected post-robotic prostatectomy surgery and containing high-density tumor areas were used for this study. DNA samples in the study were extracted from tissue and blood, which were collected prior to the prostatectomy surgery.
boolean
C3846158 (UMLS CUI [1,1])

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