This page provides instructions for visualizing DRAGEN secondary analysis outputs using HiGlass.
Cooler (.cooler) is a widely used file format for storing genomic contact matrices (e.g., Hi-C–style interactions). TruPath uses the cooler format to encode the frequency of reads aligned to pairs of genomic regions that were physically close on the flowcell, which forms a genome-wide contact map. Cooler is designed to efficiently store and query these large, sparse interaction matrices. The DRAGEN colocation cooler file can be found as <sample_name>/<sample_name>.colocation.cooler
HiGlass (https://higlass.io/), a community visualization tool for browsing genomic interaction data with smooth zooming, panning, and region-level inspection is recommended to explore colocation maps interactively.
docker pull higlass/higlass-docker # Ensure that you have the latest.
docker run --detach \
--publish 8899:80 \
--volume <local_path_to_mcooler>:/data \
--name higlass-container_8899 \
higlass/higlass-docker
Next, select your sample colocation by <project_name>/<sample_name>, as you supplied to the higlass-manage ingest command. Here, my data is in cooler-test/test-chr14.
There are also several annotation tracks that are useful, i.e. you can add tracks on top and left for chromosome and genes. You can also turn on "Toggle Position Search Box" and you can navigate to your region of interest.
t(14,21)
HiGlass also has several add-ons to support VCF, bed, and bedpe file formats. Please feel free to add those tracks on the X/Y axis and explore the proximity reads from Constellation.