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diffHic: a Bioconductor package to detect differential genomic interactions in Hi-C data.

Aaron T L Lun1,2, Gordon K Smyth3,4

  • 1The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, VIC, 3052, Melbourne, Australia. alun@wehi.edu.au.

BMC Bioinformatics
|August 19, 2015
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Summary

The diffHic software package identifies significant changes in genome interactions from Hi-C data. This tool offers a statistically rigorous approach for differential interaction analysis between biological conditions.

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Area of Science:

  • Genomics
  • Computational Biology
  • Bioinformatics

Background:

  • Chromatin conformation capture with high-throughput sequencing (Hi-C) measures in vivo genome interactions.
  • Conventional Hi-C analysis focuses on detecting significant interactions.
  • Identifying differential interactions between conditions offers a more rigorous and biologically relevant strategy.

Purpose of the Study:

  • Introduce the diffHic software package for detecting differential interactions in Hi-C data.
  • Provide a robust computational tool for analyzing changes in genome-wide interactions across biological conditions.

Main Methods:

  • diffHic offers methods for read pair alignment, processing, and counting into bin pairs.
  • Includes filtering of low-abundance events and normalization for biases (trended, CNV-driven).
  • Utilizes the edgeR package's statistical framework for modeling variability and testing differences.

Main Results:

  • diffHic successfully detects significant differential interactions in real Hi-C data.
  • The software includes options for visualizing results.
  • Evaluated performance against existing methods using simulated data.

Conclusions:

  • diffHic effectively identifies significant differences in interaction intensity between biological conditions.
  • The package demonstrates favorable performance compared to existing tools on simulated data.
  • diffHic is a viable approach for differential analyses of Hi-C data.