MACPET

MACPET analyzes paired-end ChIA-PET sequencing reads to identify protein-DNA binding sites and associated three-dimensional genomic interactions.


Key Features:

  • Input formats: Processes ChIA-PET data in BAM and SAM formats.
  • PET classification: Categorizes paired-end tags (PETs) into Self-ligated, Intra-chromosomal, and Inter-chromosomal classes.
  • Genome segmentation and modeling: Divides the genome into regions and applies two-dimensional mixture models to identify candidate peaks or binding sites.
  • Distributional modeling: Models signal and noise using skewed generalized students-t distributions (SGT) within the mixture models.
  • Statistical significance: Employs a local Poisson model to determine statistically significant binding sites.
  • Comparative performance: Shows improved motif occurrence, spatial resolution, and false discovery rate relative to MACS.
  • 3D interaction linking: Links discovered binding sites with a higher number of significant 3D genomic interactions.

Scientific Applications:

  • Protein binding site identification: Detecting protein-DNA binding sites from ChIA-PET data.
  • Chromatin architecture: Elucidating three-dimensional genomic interactions and chromatin organization.
  • Gene regulation studies: Investigating relationships between binding sites and regulatory activity relevant to gene regulation and chromatin dynamics.

Methodology:

Processes paired-end reads in BAM/SAM, classifies PETs into Self-ligated, Intra-chromosomal, and Inter-chromosomal categories, divides the genome into regions, applies two-dimensional mixture models using skewed generalized students-t distributions (SGT), and uses a local Poisson model to assess binding site significance.

Topics

Collections

Details

License:
GPL-3.0
Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
7/11/2018
Last Updated:
12/10/2018

Operations

Publications

Vardaxis I, Drabløs F, Rye MB, Lindqvist BH. MACPET: Model-based Analysis for ChIA-PET. Unknown Journal. 2018. doi:10.1101/272559.

Documentation

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