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Updated: Aug 9, 2025

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Pairtools: from sequencing data to chromosome contacts.

, Nezar Abdennur1,2, Geoffrey Fudenberg3

  • 1Program in Bioinformatics and Integrative Biology, University of Massachusetts Chan Medical School, Worcester, MA, 01605, MA.

Biorxiv : the Preprint Server for Biology
|February 24, 2023
PubMed
Summary
This summary is machine-generated.

Pairtools is a new suite of tools designed for efficient processing of chromosome conformation capture (3C+) sequencing data. It offers high-performance, flexible analysis for 3D genome organization studies.

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Area of Science:

  • Genomics
  • Molecular Biology
  • Bioinformatics

Background:

  • 3D genome organization studies generate massive sequencing data from Hi-C and related chromosome conformation capture (3C+) protocols.
  • Processing this heterogeneous data into contact pairs requires high-performance and flexible computational tools.

Approach:

  • Introducing pairtools, a modular command-line interface (CLI) toolkit for efficient contact extraction from 3C+ sequencing data.
  • Pairtools offers core and auxiliary tools for manipulating, filtering, and quality control of contact pairs.
  • The suite integrates seamlessly with Python data analysis libraries for versatile pipeline construction.

Key Points:

  • Pairtools provides protocol-specific tools for advanced analyses, including multi-way contacts, haplotype-resolved contacts, and single-cell Hi-C.
  • Benchmarking demonstrates pairtools' advantages in high-performance and flexibility compared to existing 3C+ data pipelines.
  • Its modular CLI design allows flexible chaining into custom data processing workflows.

Conclusions:

  • Pairtools offers a versatile and high-performance solution for analyzing large-scale 3D genome organization data.
  • The toolkit empowers researchers with flexible pipelines for diverse 3C+ applications.
  • Pairtools facilitates advanced genomic structure analysis through efficient contact pair processing.