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SeSAMe: reducing artifactual detection of DNA methylation by Infinium BeadChips in genomic deletions.
Zhou, Wanding; Triche, Timothy J; Laird, Peter W; Shen, Hui.
Afiliación
  • Zhou W; Center for Epigenetics, Van Andel Research Institute, 333 Bostwick Ave., N.E., Grand Rapids, MI 49503 USA.
  • Triche TJ; Center for Epigenetics, Van Andel Research Institute, 333 Bostwick Ave., N.E., Grand Rapids, MI 49503 USA.
  • Laird PW; Center for Epigenetics, Van Andel Research Institute, 333 Bostwick Ave., N.E., Grand Rapids, MI 49503 USA.
  • Shen H; Center for Epigenetics, Van Andel Research Institute, 333 Bostwick Ave., N.E., Grand Rapids, MI 49503 USA.
Nucleic Acids Res ; 46(20): e123, 2018 11 16.
Article en En | MEDLINE | ID: mdl-30085201
We report a new class of artifacts in DNA methylation measurements from Illumina HumanMethylation450 and MethylationEPIC arrays. These artifacts reflect failed hybridization to target DNA, often due to germline or somatic deletions and manifest as incorrectly reported intermediate methylation. The artifacts often survive existing preprocessing pipelines, masquerade as epigenetic alterations and can confound discoveries in epigenome-wide association studies and studies of methylation-quantitative trait loci. We implement a solution, P-value with out-of-band (OOB) array hybridization (pOOBAH), in the R package SeSAMe. Our method effectively masks deleted and hyperpolymorphic regions, reducing or eliminating spurious reports of epigenetic silencing at oft-deleted tumor suppressor genes such as CDKN2A and RB1 in cases with somatic deletions. Furthermore, our method substantially decreases technical variation whilst retaining biological variation, both within and across HM450 and EPIC platform measurements. SeSAMe provides a light-weight, modular DNA methylation data analysis suite, with a performant implementation suitable for efficient analysis of thousands of samples.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Programas Informáticos / Artefactos / Eliminación de Secuencia / Metilación de ADN / Análisis de Secuencia por Matrices de Oligonucleótidos / Ensayos Analíticos de Alto Rendimiento Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Programas Informáticos / Artefactos / Eliminación de Secuencia / Metilación de ADN / Análisis de Secuencia por Matrices de Oligonucleótidos / Ensayos Analíticos de Alto Rendimiento Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article