Optimizing ChIP-seq peak detectors using visual labels and supervised machine learning.

Journal: Bioinformatics (Oxford, England)
Published Date:

Abstract

MOTIVATION: Many peak detection algorithms have been proposed for ChIP-seq data analysis, but it is not obvious which algorithm and what parameters are optimal for any given dataset. In contrast, regions with and without obvious peaks can be easily labeled by visual inspection of aligned read counts in a genome browser. We propose a supervised machine learning approach for ChIP-seq data analysis, using labels that encode qualitative judgments about which genomic regions contain or do not contain peaks. The main idea is to manually label a small subset of the genome, and then learn a model that makes consistent peak predictions on the rest of the genome.

Authors

  • Toby Dylan Hocking
    Department of Human Genetics, McGill University, H3A-1A4, Montréal, Canada.
  • Patricia Goerner-Potvin
    Department of Human Genetics, McGill University, H3A-1A4, Montréal, Canada.
  • Andreanne Morin
    Department of Human Genetics, McGill University, H3A-1A4, Montréal, Canada.
  • Xiaojian Shao
    Department of Human Genetics, McGill University, H3A-1A4, Montréal, Canada.
  • Tomi Pastinen
    Department of Human Genetics, McGill University, H3A-1A4, Montréal, Canada.
  • Guillaume Bourque
    Department of Human Genetics, McGill University, H3A-1A4, Montréal, Canada.