Genetic Basis of Melanocytic Nevi
- Conditions
- Melanocytic Nevi
- Registration Number
- NCT03054584
- Lead Sponsor
- University of California, Davis
- Brief Summary
The objective of this protocol is to further elucidate the genetic mutations that drive melanocytic nevi (benign melanocytic neoplasms, moles). This will be performed by whole genome, whole exome, or targeted sequencing of de-identified specimens.
Herein, the investigators plan to isolate DNA from de-identified skin biopsy specimens and blood samples:
1. From melanocytic nevi collected by skin biopsy (a shave or punch biopsy). A part of the tissue will be submitted for routine diagnostic dermatopathology and investigational histomorphologic and immunohistochemical analysis.
2. From corresponding normal tissue (blood). DNA isolated from blood will be used as a normal control when analyzing sequencing data to identify somatic mutations in lesional tissue.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 50
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Genome Wide Mutation Analysis Feb 2017 - December 2018 Will be performing genome wide mutation analysis to quantify the number of mutations.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of California-Davis, Department of Dermatology
🇺🇸Sacramento, California, United States