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You will probably end up with inaccurate results, or more specifically you'll likely end up finding fewer active viruses than there actually are. If you separate the viruses (most of the under 0.2 micron) from the greater than 0.2 micron fraction then you are separating a lot of the active viruses (their genome copies). You can run propagate on the greater than 0.2 micron and capture some active viruses. You can't really combine the sequencing results from the two fractions because the coverage ratios will not be accurate. You can try running propagate but keep these caveats in mind.
I filtered my samples at .2 microns and then I also sequenced the free floating section. How will this affect my use of your program?
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