Motivation: High-throughput measurements of DNA methylation are increasingly becoming a mainstay of biomedical investigations. While the methylation status of individual cytosines can sometimes be informative, several recent papers have shown that the functional role of DNA methylation is better captured by a quantitative analysis of the spatial variation of methylation across a genomic region. Results: Here, we present BPRMeth, a Bioconductor package that quantifies methylation profiles by generalized linear model regression. The original implementation has been enhanced in two important ways: we introduced a fast, variational inference approach that enables the quantification of Bayesian posterior confidence measures on the model, and we adapted the method to use several observation models, making it suitable for a diverse range of platforms including single-cell analyses and methylation arrays.

BPRMeth: a flexible Bioconductor package for modelling methylation profiles / Kapourani, Ca; Sanguinetti, G. - In: BIOINFORMATICS. - ISSN 1367-4803. - 34:14(2018), pp. 2485-2486. [10.1093/bioinformatics/bty129]

BPRMeth: a flexible Bioconductor package for modelling methylation profiles

Sanguinetti G
2018-01-01

Abstract

Motivation: High-throughput measurements of DNA methylation are increasingly becoming a mainstay of biomedical investigations. While the methylation status of individual cytosines can sometimes be informative, several recent papers have shown that the functional role of DNA methylation is better captured by a quantitative analysis of the spatial variation of methylation across a genomic region. Results: Here, we present BPRMeth, a Bioconductor package that quantifies methylation profiles by generalized linear model regression. The original implementation has been enhanced in two important ways: we introduced a fast, variational inference approach that enables the quantification of Bayesian posterior confidence measures on the model, and we adapted the method to use several observation models, making it suitable for a diverse range of platforms including single-cell analyses and methylation arrays.
2018
34
14
2485
2486
Kapourani, Ca; Sanguinetti, G
File in questo prodotto:
File Dimensione Formato  
bty129.pdf

accesso aperto

Descrizione: Open Access article
Tipologia: Versione Editoriale (PDF)
Licenza: Creative commons
Dimensione 169.83 kB
Formato Adobe PDF
169.83 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11767/117250
Citazioni
  • ???jsp.display-item.citation.pmc??? 8
  • Scopus 9
  • ???jsp.display-item.citation.isi??? 9
social impact