This fastq was generated by training Nanosim (https://github.com/bcgsc/NanoSim - v.2.3.2) on a set of real LASV sequencing runs and then generating a set of artificial LASV reads with some contaminants (Human, bacterial and other virus reads):

1. Map reads to LASV reference genome (L and S segment)
2. Train Nanosim with mapped reads and LASV reference as reference for error rate
3. Simulate a set of 10000 reads with the following abundances:
	Size	10000
	Homo_sapiens	40
	LASV_S	15
	LASV_L	15
	fecal_virus	10
	Cutibacterium	10
	MS2	10
4. Nanosim sometimes generated reads that indicate circular genomes that are not depicting the reality, so these reads were removed 

=> ~9000 artificial reads to test if ViMOP runs smoothly.

Run should take around 10 minutes depedning on how occupied the system is.