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Cross-domain #4
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Hi Nico, Unless the other input (than microbiome) also can be assumed to follow generalized Lotka-Volterra models. Otherwise, it might require to rewrite the model and derive the EM optimization. Chenhao |
Hi,
The other input is also a phyloseq object of the viral community.
In total I have 2 phyloseq objects: one from the bacterial and another from
the viral community.
Le mar. 9 févr. 2021 19 h 20, Chenhao Li <[email protected]> a
écrit :
… Hi Nico,
Unless the other input (than microbiome) also can be assumed to follow
generalized Lotka-Volterra models. Otherwise, it might require to rewrite
the model and derive the EM optimization.
Chenhao
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I think you could try using them as a single taxanomic matrix then. |
But the 2 objects come from different sequencing run/approach.
Le mar. 9 févr. 2021 20 h 03, Chenhao Li <[email protected]> a
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… I think you could try using them as a single taxanomic matrix then.
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I see. I think it is a bit tricky because we will need the ratio of bacteria vs. virus in each sample... |
I don't have that...At best I have the relative abundance of each taxa for
each table...
Le mar. 9 févr. 2021 20 h 15, Chenhao Li <[email protected]> a
écrit :
… I see. I think it is a bit tricky because we will need the ratio of
bacteria vs. virus in each sample...
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Hi,
I wonder if it would be possible to analyse cross domain interactions like with Spiec-easi? In that case, input would be 2 tables.
Thanks,
Nico
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