vargram 0.3.0

A Python visualization tool for genomic surveillance

VARGRAM (Visual ARrays for GRaphical Analysis of Mutations)

🧬 VARGRAM is a Python package that makes it easy to generate insightful figures for genomic surveillance, born out of our experience during the COVID-19 pandemic. With the latest update, VARGRAM can be used to generate mutation profiles straight from sequence files by hooking into existing tools such as Nextclade. The figures can be easily customized within a Python script or Jupyter notebook using a declarative syntax.

🔥 We are actively developing VARGRAM into a full visualization library for common use cases in molecular epidemiology. More modules will be added in the coming months. If you have a feature request or find a bug, please submit an issue.

Documentation

Full installation instructions and tutorials are available on the VARGRAM documentation website.

Installation

Install with pip:

pip install vargram

Python version ≥3.11 is required.

VARGRAM relies on Nextclade to perform mutation calling when sequence files are provided. Make sure to download the Nextclade CLI and add it to the path. (Alternatively, you may provide Nextclade's analysis CSV output directly and VARGRAM can still produce a mutation profile without Nextclade installed.)

Quickstart Guide

To produce a mutation profile, VARGRAM requires a single FASTA file (or a directory of FASTA files) of samples, a FASTA file for the reference, and a genome annotation file following the GFF3 format.

A mutation profile can be generated in just four lines of code:

from vargram import vargram # Importing the package

vg = vargram(seq='path/to/covid_samples/', # Provide sample sequences
            ref='path/to/covid_reference.fa', # Provide reference sequence
            gene='path/to/covid_annotation.gff') # Provide genome annotation
vg.profile() # Tell VARGRAM you want to create a mutation profile
vg.show() # And show the resulting figure

Alternatively, you can simply provide a CSV file. For example, you can upload your sequences to the Nextclade web app and download the analysis CSV output. VARGRAM recognizes this output and can process it:

from vargram import vargram

vg = vargram(data='path/to/nextclade_analysis.csv') # Provide Nextclade analysis file
vg.profile()
vg.show()

Calling the mutation profile this way does not require Nextclade CLI to be installed.

Sample Output

A sample mutation profile is shown below:

Note that by default, VARGRAM favors placing genes with the most number of mutations first. Thus, the S gene above is shown at the very top. You may wish to force VARGRAM to show the genes in order based on the start position. You can do so by setting vg.profile(order=True). The mutation profile above will then look like the following: