Viral lineages and variants pose high risk to global public health.
VIRUS-MVP is a heatmap-centric visualization web application that encodes mutational information across multiple groups, including SARS-CoV-2 lineages. The data visualized by VIRUS-MVP is generated by two external projects:
You can find deployed versions of this application (without user upload functionality) at https://virusmvp.org/.
$ git clone git@github.com:cidgoh/VIRUS-MVP.git --recurse-submodules
We use Conda, but you can use venv.
$ conda create --name=VIRUS-MVP
$ conda activate VIRUS-MVP
(VIRUS-MVP) $ pip install -r requirements.txt
If you do not run the application from the root directory, some of the JavaScript assets will not be compiled.
(VIRUS-MVP) $ python app.py
Go to http://0.0.0.0:8050/.
Click the help button 
at the top for an in-app explanation of the
heatmap view.
The left axis encodes viral lineages. Lineages belonging to VOC are in
bold, and lineages belonging to VOI are in italics. Actively circulating
lineages are denoted with
The right axis encodes the number of genomic sequences analyzed for each lineage.
The top axis encodes the nucleotide position of lineage mutations, with respect to the reference genome.
The bottom axis encodes the amino acid position of lineage mutations, in the following format:
Genic mutations: {GENE}.{AMINO ACID POSITION WITHIN THAT GENE}
Intergenic: {NEAREST DOWNSTREAM GENE}. {NUMBER OF NUCLEOTIDES UPSTREAM}
The heatmap cells encode the presence of mutations. The color of these cells encodes mutation frequency. Insertions, deletions, functional mutations, and lineages with a sample size of one are encoded as follows:
Hovering over cells displays detailed mutation information. Clicking cells opens a modal with detailed mutation function descriptions, and their citations.
The histogram bars encode the total number of mutations across all visualized lineages every 100 nucleotide positions.
There are several tools in the top of the interface that can be used to edit the visualization.
Clicking the select lineages btn 
opens a modal that
allows you to rearrange and hide variants.
The mutation frequency slider allows you to filter heatmap cells by mutation frequency.
The clade defining switch allows you to filter in and out heatmap cells corresponding to non-clade defining mutations.
The upload button 
allows you to upload your own genomic data in
FASTA or VCF format. You can find examples of files users can upload in
test_data/.
You must have Nextflow and Conda installed to upload files.
Your first upload will take a while. Subsequent uploads will be faster.
The download button 
allows you to download a zip object
containing surveillance reports for each reference variant. You can find
examples of these reports in surveillance_reports/.
Nextflow-wrapped workflow for variant calling.
Repository for mutation functions.
We encourage you to add any problems with the application as an issue in this repository, but you can also email us at contact@cidgoh.ca.
@ivansg44: Visualization development
@anwarMZ: Genomic analysis
@Anoosha-Sehar: Functional annotation
@miseminger: Functional annotation and data standardization
@despean: Application deployment
William Hsiao, Gary Van Domselaar, and Paul Gordon
The results here are in whole or part based upon data hosted at the Canadian VirusSeq Data Portal: https://virusseq-dataportal.ca/. We wish to acknowledge the following organisations/laboratories for contributing data to the Portal: Canadian Public Health Laboratory Network (CPHLN), CanCOGGeN VirusSeq, Saskatchewan - Roy Romanow Provincial Laboratory(RRPL), Nova Scotia Health Authority, Alberta ProvLab North(APLN), Queen's University / Kingston Health Sciences Centre, National Microbiology Laboratory(NML), BCCDC Public Health Laboratory, Public Health Ontario(PHO), Newfoundland and Labrador - Eastern Health, Unity Health Toronto, Ontario Institute for Cancer Research(OICR), Manitoba Cadham Provincial Laborator, and Manitoba Cadham Provincial Laboratory.