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Discovery of Novel Melanoma Predisposing Mutations by Exome Sequencing

ABSTRACT:

Melanoma risk shows clear heritability, but the inherited genetic factors remain largely unknown. Rare high risk mutations in CDKN2A, CDK4, BAP1 and TERT have been described but these variants, in aggregate, account for less than 50% of the kindreds reporting a family history of melanoma. This project will seek to identify new genes which may confer melanoma susceptibility. Identifying melanoma predisposing mutations can provide new biological insights and may impact important clinical decision making regarding treatment, surveillance and preventive approaches. Hereditary melanoma patients (defined as those individuals with multiple primary melanomas and those patients with a family history of melanoma) were collected from melanoma clinics at the Massachusetts General Hospital in Boston and the A. Sygrous Hospital in Athens, Greece.

All exome sequencing was performed at the Broad Institute of Harvard and MIT; samples sequence capture was performed using Agilent SureSelect Human All Exon Kit v2 and sequencing was performed on an Illumina HiSeq 2000 or 2500.

PROVIDER: phs000823 | dbGaP |

SECONDARY ACCESSION(S): PRJNA264594PRJNA264595

REPOSITORIES: dbGaP

ACCESS DATA

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Dataset's files

Source:

			Action	DRS
	GapExchange_phs000823.v1.p1.xml	Xml
	dbGaPEx2.1.5.xsd	Other
	Study_Report.phs000823.MelanomaNovelCancerPredisposingMutations.v1.p1.MULTI.pdf	Pdf
	manifest_phs000823.MelanomaNovelCancerPredisposingMutations.v1.p1.c1.DS-CA.pdf	Pdf
	manifest_phs000823.MelanomaNovelCancerPredisposingMutations.v1.p1.c2.GRU.pdf	Pdf

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