ID

45743

Descripción

Principal Investigator: Rose Yang, PhD, National Institutes of Health, Bethesda, MD, USA MeSH: Melanoma, Cutaneous Malignant https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001177 Although a number of high-risk melanoma genes have been identified, they account for melanoma risk in less than 40% of melanoma-prone families. The major goals of our research are to identify novel high-penetrance genes for familial melanoma in melanoma-prone families without known mutations and to identify modifier factors, including genetic and epigenetic, in melanoma-prone families with and without known major mutations. We are using whole exome sequencing to identify additional high-risk susceptibility genes and using targeted sequencing to follow up on the top genes in additional family members and in population-based melanoma cases and controls. We are also using RNASeq to investigate genome-wide allele-specific expression and eQTLs in these families to identify genes with expression alteration, which will provide additional information for gene discovery. In addition, we also conducted genome-wide copy number variation (CNV), methylation, and miRNA expression profiling analyses in our melanoma families with the goal of identifying genetic and epigenetic factors as disease modifiers.

Link

dbGaP-study=phs001177

Palabras clave

Versiones (1)

1. 2/6/23 2/6/23 - Chiara Middel

Titular de derechos de autor

Rose Yang, PhD, National Institutes of Health, Bethesda, MD, USA

Subido en

2 de junio de 2023

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia