This repo contains the source code of the algorithm for finding the optimal set of Topologically Associating Domains (TADs) using a combination of Hi-C and ChIP-seq/DNAme data. The algorithm is implemented in Python and is suitable for the identification of optimized TAD partitions across different resolutions in Drosophila and mammalian species.

Getting Started

Dependencies

To successfully run optimalTAD you will need to install the following dependencies:

• C++11
• Python 3
• MPICH2 or Open MPI (for parallel computing)
• boost (for macOS)

Also, one can set up a conda environment with all required dependencies installed using the following .yml files:

Linux users:

conda env create -f environment_optimaltad_linux64.yml

macOS users:

brew install boost # if boost libraries are not installed yet 
conda env create -f environment_optimaltad_osx.yml

Please note that the algorithm was tested on Linux and macOS operating systems only, therefore we can't guarantee that it will work on Windows as well.

Installation

Clone this repo and install optimalTAD using pip:

git clone https://github.com/cosmoskaluga/optimalTAD
cd optimalTAD
./install.sh

Usage

To launch the algorithm type the following at the command line:

optimalTAD run [-h] [--hic HIC [HIC ...]] [--chipseq CHIPSEQ [CHIPSEQ ...]] [--np NP] [--resolution RESOLUTION] [--stepsize STEPSIZE] [--gamma_max GAMMA_MAX]
                  [--hic_format HIC_FORMAT] [--empty_row_imputation] [--truncation] [--log2_hic] [--log2_chip] [--zscore_chip] [--mammal] [--window_size_min WINDOW_SIZE_MIN]
                  [--window_size_max WINDOW_SIZE_MAX]

Required and optional arguments:

-h, --help                              Help message
--hic HIC [HIC ...]                     Iteratively corrected Hi-C matrices in .hdf5 or .cool format
--chipseq CHIPSEQ [CHIPSEQ ...]         Epigenetic data (ChIP-seq in .bedgraph or .bw format)
--np [NP]                               Number of processors (=1)
--resolution [RESOLUTION]               Resolution of Hi-C matrices (=1)
--stepsize [STEPSIZE]                   Step size to increment gamma parameter in Armatus (=0.05)
--gamma_max [GAMMA_MAX]                 Max value of the gamma parameter (=4)
--hic_format [HIC_FORMAT]               Hi-C matrices input format for armatus (=txt.gz)
--empty_row_imputation                  Empty line imputation (=False)
--truncation                            Truncation of a Hi-C-matrix (=False)
--log2_hic                              log2 transformation of Hi-C matrix (=False)
--log2_chip                             log2 transformation of ChIP-seq values (=False)
--zscore_chip                           Z-score transformation of ChIP-seq values(=False)
--mammal                                Input data is derived from mammalian species (=False)
--window_size_min [WINDOW_SIZE_MIN]     Minimal window size in insulation score method (for mammals only!)
--window_size_max [WINDOW_SIZE_MAX]     Maximal window size in insulation score method (for mammals only!)  

All listed arguments can also be specified in the config.ini configuration file.

Both Hi-C and ChIP-Seq data are required for optimalTAD running. We strongly recommend you perform iterative correction (Imakaev et al, 2012) on your Hi-C data before running optimalTAD. ChIP-seq coverage track should be normalized by input and stored in .bedgraph or .bw file. No further preparation of ChIP-seq data is required, the algorithm will binarize coverage with respect to a chosen resolution of the Hi-C map and provide log2 and z-score transformation if needed.

Note: optimalTAD utilizes the two well-known TAD calling algorithms to produce all possible TAD sets and the choice of method depends on the species type input data originates from. The default method is Armatus, which is recommended for the analysis of Drosophila's topological domains. If you work with mammalian contact maps (--mammals argument), optimalTAD switches to the Insulation Score (IS) method from cooltools package.

Running on test data

First, execute test_data.sh script:

chmod a+x ./test_data.sh
./test_data.sh

It will create testdata folder containing Hi-C and ChIP-seq data of Drosophila chromosome 2L. Next, run optimalTAD:

optimalTAD run

Visualizing results

Hi-C data with the obtained optimal TAD set can be visualized using the function below:

optimalTAD visualize [-h] [--samplename SAMPLENAME] [--region REGION] [--resolution RESOLUTION] [--chipseq CHIPSEQ] [--log2_chip] [--zscore_chip] [--rnaseq RNASEQ]

with the following arguments:

-h, --help                          Help message
--samplename SAMPLENAME             Samplename of Hi-C data (for example, LacZ_1)
--region REGION                     Genome region to plot (for example, chr2L:1,000,000-5,000,000)
--resolution RESOLUTION             Resolution of Hi-C matrix (=1)
--chipseq CHIPSEQ                   Path to epigenetic data
--log2_chip                         log2 transformation of epigenetic data
--zscore_chip                       Z-score transformation of epigenetic data
--rnaseq RNASEQ                     Add additional track to the plot

Documentation

optimalTAD documentation is available on readthedocs.

How to cite

"optimalTAD: annotation of topologically associating domains based on chromatin marks enrichment." Dmitrii N. Smirnov, Anna D. Kononkova, Debra Toiber, Mikhail S. Gelfand, Ekaterina E. Khrameeva bioRxiv 2023.03.06.531254; doi: https://doi.org/10.1101/2023.03.06.531254

Manuscript

Scripts reproducing the main analyses from the manuscript can be found here: https://github.com/cosmoskaluga/optimaltad_manuscript_analysis