Papers
Topics
Authors
Recent
Assistant
AI Research Assistant
Well-researched responses based on relevant abstracts and paper content.
Custom Instructions Pro
Preferences or requirements that you'd like Emergent Mind to consider when generating responses.
Gemini 2.5 Flash
Gemini 2.5 Flash 134 tok/s
Gemini 2.5 Pro 41 tok/s Pro
GPT-5 Medium 23 tok/s Pro
GPT-5 High 18 tok/s Pro
GPT-4o 86 tok/s Pro
Kimi K2 194 tok/s Pro
GPT OSS 120B 432 tok/s Pro
Claude Sonnet 4.5 37 tok/s Pro
2000 character limit reached

BayMeth: Improved DNA methylation quantification for affinity capture sequencing data using a flexible Bayesian approach (1312.3115v1)

Published 11 Dec 2013 in q-bio.GN and q-bio.QM

Abstract: DNA methylation (DNAme) is a critical component of the epigenetic regulatory machinery and aberrations in DNAme patterns occur in many diseases, such as cancer. Mapping and understanding DNAme profiles offers considerable promise for reversing the aberrant states. There are several approaches to analyze DNAme, which vary widely in cost, resolution and coverage. Affinity capture and high-throughput sequencing of methylated DNA strike a good balance between the high cost of whole genome bisulphite sequencing (WGBS) and the low coverage of methylation arrays. However, existing methods cannot adequately differentiate between hypomethylation patterns and low capture efficiency, and do not offer flexibility to integrate copy number variation (CNV). Furthermore, no uncertainty estimates are provided, which may prove useful for combining data from multiple protocols or propagating into downstream analysis. We propose an empirical Bayes framework that uses a fully methylated (i.e. SssI treated) control sample to transform observed read densities into regional methylation estimates. In our model, inefficient capture can be distinguished from low methylation levels by means of larger posterior variances. Furthermore, we can integrate CNV by introducing a multiplicative offset into our Poisson model framework. Notably, our model offers analytic expressions for the mean and variance of the methylation level and thus is fast to compute. Our algorithm outperforms existing approaches in terms of bias, mean-squared error and coverage probabilities as illustrated on multiple reference datasets. Although our method provides advantages even without the SssI-control, considerable improvement is achieved by its incorporation. Our method can be applied to methylated DNA affinity enrichment assays (e.g MBD-seq, MeDIP-seq) and a software implementation is available in the Bioconductor Repitools package.

Summary

We haven't generated a summary for this paper yet.

Dice Question Streamline Icon: https://streamlinehq.com

Open Problems

We haven't generated a list of open problems mentioned in this paper yet.

Lightbulb Streamline Icon: https://streamlinehq.com

Continue Learning

We haven't generated follow-up questions for this paper yet.

List To Do Tasks Checklist Streamline Icon: https://streamlinehq.com

Collections

Sign up for free to add this paper to one or more collections.