Heritable DNA methylation marks associated with susceptibility to breast cancer.
Ontology highlight
ABSTRACT: Mendelian-like inheritance of germline DNA methylation in cancer susceptibility genes has been previously reported. We aimed to scan the genome for heritable methylation marks associated with breast cancer susceptibility by studying 25 Australian multiple-case breast cancer families. Here we report genome-wide DNA methylation measured in 210 peripheral blood DNA samples provided by family members using the Infinium HumanMethylation450. We develop and apply a new statistical method to identify heritable methylation marks based on complex segregation analysis. We estimate carrier probabilities for the 1000 most heritable methylation marks based on family structure, and we use Cox proportional hazards survival analysis to identify 24 methylation marks with corresponding carrier probabilities
SUBMITTER: Joo JE
PROVIDER: S-EPMC5830448 | biostudies-literature | 2018 Feb
REPOSITORIES: biostudies-literature
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