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.
DOI: 10.1101/272559