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Updated: May 5, 2026

Optimized Analysis of DNA Methylation and Gene Expression from Small, Anatomically-defined Areas of the Brain
Published on: July 12, 2012
AutoMethyc: an automated methylation analysis for massively parallel sequencing data
Fernando Ambriz-Barrera1,2, Miguel Ruiz-De La Cruz1,2, Héctor Martínez-Gregorio1,2
1National Laboratory on Health, Molecular Diagnostics and Environmental Effects on Chronic-Degenerative Diseases, Faculty of Higher Studies Iztacala, UNAM, Avenida de los Barrios #1, Los Reyes Iztacala, Tlanepantla, 54090, Mexico State, Mexico.
Motivation:
Bisulfite sequencing (BS-Seq) enables a comprehensive and detailed analysis of DNA methylation patterns at single-nucleotide resolution. While methylation differences can contribute to various diseases, their sincronous occurrence at distinct loci complicates understanding. Therefore, advanced tools are essential to facilitate the identification and analysis of methylation programs and patterns.
Results:
AutoMethyc provides a comparative approach by integrating different algorithms coordinated and optimized for use on desktop computers and servers. The workflow evaluates the methylation status from different perspectives, facilitating interpretation in an interactive HTML report, incorporating new co-methylation analyses for marker identification, as well as exploratory complex workflows with dimension reduction techniques and identification of unsupervised groups between samples or sites. AutoMethyc was tested in a breast cancer study ($n=389$; 233 cases and 156 controls) using BS-Seq data from the Illumina MiSeq platform, mapping 330 methylation-prone citocine (CpG) sites in 20 genes. The analysis was performed on a desktop with 64 GB RAM, 16 cores (4.673 GHz), and 326 KB/s internet, running Fedora 39 with i3wm. The tool processed the dataset in 48 h, showcasing its efficiency and scalability.

