Fig 1.
Workflow diagram of the analysis done for the SILVA database and the GTDB.
The SILVA and GTDB were downloaded and sequences with incomplete taxonomic labels or from mitochondria and plastids were removed. To create the simulated databases for each marker gene, we created a collection of random subsets varying in size from 10,000 to 200,000 sequences in 10,000 gene increments. Each simulated database was clustered at 95%, 97%, 99%, and 100% identity requiring that shorter sequences fully align to longer ones.
Fig 2.
Clustering analysis for simulated databases created by randomly sampling sequences from the 16S rRNA SILVA database and the 120 marker gene Genome Taxonomy Database (GTDB).
Each simulated database was clustered at 95%, 97%, 99%, and 100% identity requiring that shorter sequences fully align to longer ones. The 16S rRNA gene is denoted by a star in all subplots. A) The relationship between the number of genes in the simulated databases, the number of clusters, the number of multi-species clusters, and the number of sequences in multi-species clusters. For GTDB, each curve is for one of the 120 marker genes. B) The rate at which sequences were recruited to multi-species clusters as the database grows. Each point represents one of the 120 marker genes in the GTDB. C) The percentage of species with sequences in multi-species clusters. D) The relationship between the number of multi-species clusters that a species belongs to and the species richness of its genus (i.e., the total number of species from that genus) in the simulated database. This data was only taken from the final iteration of the simulated databases. The results were aggregated across all 120 marker genes in the GTDB.
Fig 3.
Workflow diagram of the analysis done for the Listeria marker gene simulated databases (16S rRNA and 40 marker genes).
First, 5,014 Listeria draft genomes were downloaded from RefSeq and the 16S rRNA and 40 markers genes were predicted with Barnap and FetchMG, respectively. Genes that were below half or above twice as long as the mean length for a specific marker gene were removed. To create the simulated databases for each marker gene, we randomly subsampled the sequences into subsets varying in size from 1,000 to 5,000 sequences in 1,000 gene increments. We repeated this process 100 times so we could estimate the variability of our results. Each simulated database was clustered at 95%, 97%, 99%, and 100% identity requiring that shorter sequences fully align to longer ones.
Fig 4.
Clustering analysis for the simulated databases created by randomly sampling sequences from the 16S rRNA and the 40 marker genes extracted from 5,014 Listeria genomes.
Each simulated database was clustered at 95%, 97%, 99%, and 100% identity requiring that shorter sequences fully align to longer ones. The results for each gene are reported by the median over 100 bootstrap experiments. The 16S rRNA gene is denoted by a star in all subplots. A) The relationship between the number of genes in the simulated databases, the number of clusters, the number of multi-species clusters, and the number of sequences in multi-species clusters. Each curve represents one of the 40 marker genes. The starred curve represents the 16S rRNA gene B) The rate at which sequences were recruited to multi-species clusters as the database grows. Each point represents one of the 40 marker genes. C) The percentage of species with sequences in multi-species clusters.