Command Line Workflow

For these analyses, we'll be starting with an aligned, trimmed, and sorted BAM file, test.bam. Alignment can be done using a variety of methods, including minimap2 and bwa. For information on how to perform trimming and sorting, check out the iVar manual.

Once you've got your BAM file, you'll just need the reference that you used for the alignment (i.e. Hu-1 for SARS-CoV-2 samples, like this). Since we're generally going to be working with many wastewater samples at the same time, it's a good idea to create folders to store each of the output files, using mkdir variants_files depth_files demix_files, for example. From there you can go ahead and run initial single nucleotide variant (SNV) calling step, in which we calculate the frequency of each observed mutation in the data.

This can be done using the command

freyja variants test.bam --variants variants_files/test.variants.tsv --depths depth_files/test.depth --ref NC_045512_Hu-1.fasta

Before we perform demixing, it's a good idea to make sure our list of lineage barcodes and corresponding metadata is up to date. We can do this by running

freyja update

which will save these files in freyja's data folder. This can be a bit tricky to find in your conda environment, so if you want a local copy (good to keep around in case you want to compare results with past/future barcode libraries) you can also add in the --outdir option, and specify the location where you want to put the barcode library. This just needs to be done once (per session -- new lineages are being added every day), and then we can proceed to the de-mixing step. Demixing can be performed using the command

freyja demix variants_files/test.variants.tsv depth_files/test.depth --output demix_files/test.output --confirmedonly

If you want to use your local barcodes set, you'll need to use the --barcodes option and specify the path of your local barcodes. Note: While the output of freyja variants will not change over time, the output of freyja demix depends strongly on the list of known lineage barcodes. The method will assign the closest lineage (in an edit distance sense) to what's in the data, but if a more representative lineage is identified the assignment will shift to the more representative lineage.

Once you've run demix on a bunch of samples, you can aggregate all of the output files using the command

freyja aggregate demix_files/ --output bunch_of_files.tsv.

From there, it's easy to look directly at the output files in any standard tsv viewer (Excel, Numbers, LibreOffice Calc, etc.).