Closed LeeBergstrand closed 1 year ago
So we map the reads to the combined set of contigs of the representative MAGs.
I suggest to use the median coverage for relative abundance calculation. And the counts if you want /need counts.
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Thank you for your contributions.
I am trying to determine each dereplicated MAG's abundance in each sample.
The counts folder within genomes contains four files:
Can you provide an overview of what each file contains and how each is generated?
For example, the counts_genomes.parquet file appears to contain the number of reads mapping from each metagenome to each MAG. Is this correct?