I am using GRiD to evaluate growth rates of metagenome assembled genomes in multiple samples, metagenomic sequencing depth for samples varies a lot, so I am wondering whether should I subset all the metagenomic datasets to an even depth.
Typically, higher coverage results in more accurate predictions and factors such as genome fragmentation may affect the output. I think you should be ok with genome coverage >= 1X.
Hi,
I am using GRiD to evaluate growth rates of metagenome assembled genomes in multiple samples, metagenomic sequencing depth for samples varies a lot, so I am wondering whether should I subset all the metagenomic datasets to an even depth.
Thanks a lot !