Monoallelic gene inference from chromatin (MaGIC)

Monoallelic gene inference from chromatin (MaGIC) infers monoallelically expressed (MAE) versus biallelically expressed (BAE) genes by analyzing chromatin-mark enrichment from ChIP-seq using machine learning.


Key Features:

  • Sequence-independent chromatin signature: Uses a sequence-independent chromatin signature derived from chromatin-mark enrichment to identify MAE with high sensitivity and specificity across tissue types.
  • ChIP-seq input: Operates on ChIP-seq chromatin mark enrichment data as the primary input for inference.
  • Model flexibility and machine learning: Applies machine learning classification with support for applying pre-existing models or training new models using additional chromatin marks.

Scientific Applications:

  • Random monoallelic expression analysis: Enables study of epigenetic mechanisms such as random MAE involving allele-specific expression that varies between clonal cell lineages.
  • MAE mapping across tissues: Facilitates mapping of MAE across diverse cell and tissue types to investigate cell-type-specific gene expression and epigenetic regulation.
  • Biological and translational research: Provides data and classifications relevant to developmental biology, cancer research, and personalized medicine.

Methodology:

MaGIC analyzes chromatin marks from ChIP-seq to derive a sequence-independent chromatin signature and applies machine learning models to classify genes as MAE or BAE, with options to use pre-existing models or train new models using additional chromatin marks.

Topics

Details

License:
MIT
Maturity:
Mature
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Linux, Mac
Programming Languages:
R
Added:
5/18/2019
Last Updated:
6/16/2020

Operations

Publications

Vinogradova S, Saksena SD, Ward HN, Vigneau S, Gimelbrant AA. MaGIC: a machine learning tool set and web application for monoallelic gene inference from chromatin. BMC Bioinformatics. 2019;20(1). doi:10.1186/s12859-019-2679-7. PMID:30819107. PMCID:PMC6394031.

PMID: 30819107
PMCID: PMC6394031
Funding: - National Institutes of Health: GM114864