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Updated: May 18, 2026

A Novel Bayesian Change-point Algorithm for Genome-wide Analysis of Diverse ChIPseq Data Types
Published on: December 10, 2012
Comb-p: software for combining, analyzing, grouping and correcting spatially correlated P-values.
Brent S Pedersen1, David A Schwartz, Ivana V Yang
1Department of Medicine, University of Colorado, Denver, Anschutz Medical Campus, Aurora, CO 80045, USA. bpederse@gmail.com
comb-p is a versatile command-line tool and Python library for analyzing P-values. It facilitates P-value manipulation, including combining adjacent values and identifying enriched regions for various genomic applications.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- The comb-p tool is available under the BSD license.
- Documentation and source code are accessible via GitHub.
Purpose of the Study:
- To introduce comb-p, a flexible command-line tool and Python library.
- To provide functionalities for P-value manipulation and analysis in genomic data.
Main Methods:
- Utilizes BED files for handling P-values of varying spacing.
- Implements functions for auto-correlation, P-value combination, and false discovery rate adjustment.
- Includes methods for identifying and assessing regions of P-value enrichment.
Main Results:
- Demonstrates validation and application on bisulfite-seq, tiled methylation probes, and Dam-ID data.
- Shows utility with P-values derived from Fisher's exact test, linear models, and moderated t-statistics.
- Highlights the tool's adaptability due to its standardized input format and P-value origin independence.
Conclusions:
- comb-p offers a comprehensive solution for P-value analysis across diverse genomic applications.
- The tool's flexibility makes it suitable for a wide range of biological research questions.
- Provides integrated visualization and assessment tools for enhanced data interpretation.
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