<p>For each of the fifteen monophyletic sequence clusters, the number of serotypes it contained was plotted against (A) the number of representatives of the sequence cluster; (B) the overall genetic diversity of the sequence cluster, as represented by the number of polymorphic sites identified from whole genome alignments; (C) the number of point mutations reconstructed as having occurred over the history of the sequence cluster; and (D) the number of homologous recombination events reconstructed as having occurred over the history of the sequence cluster.</p
<p>The concordance was based on the proportion of genomes in a cgMLST cluster that belonged to the p...
<p>Twelve representative CCGs are shown in (A) PCA plot where principle component analysis (PCA) of ...
<p>The proportion of closely related sequences in each of the five clusters shown in <a href="http:/...
<p>Panels (A) and (B) are based on all protein-coding genes, panels (C) and (D) are based on the put...
Prevalence of mutations identified in clusters by phylogenetic analysis of 251 sequences with drug r...
<p><i>N</i>, number of individuals sequenced; VS, variable sites; PIS, parsimony information sites; ...
BACKGROUND: The distribution of human disease-associated mutations is not random across the human ge...
<p>(A) Mutation prevalences across time series. (B) One of 51 recombination networks that fit the da...
Comparing chromosomal gene order in two or more related species is an important approach to studying...
<p>The maximum likelihood phylogeny derived from a codon alignment of ‘core’ protein coding sequence...
<p>A) Chromosome 5 near <i>TMEM161B</i> and <i>MEF2C</i>, B) Chromosome 17 on <i>SFRS2</i> and C) Ch...
<p>The maximum likelihood phylogeny was inferred from the concatenated protein alignment of 2,374 si...
<p>For each locus (<i>FRI</i> [A], <i>Rpm1</i> [B], <i>Rps2</i> [C], and <i>Rps5</i> [D]), the botto...
<div><h3>Background</h3><p>The distribution of human disease-associated mutations is not random acro...
<p>The x-axis represents geographic locations where the isolates were collected. The y-axis represen...
<p>The concordance was based on the proportion of genomes in a cgMLST cluster that belonged to the p...
<p>Twelve representative CCGs are shown in (A) PCA plot where principle component analysis (PCA) of ...
<p>The proportion of closely related sequences in each of the five clusters shown in <a href="http:/...
<p>Panels (A) and (B) are based on all protein-coding genes, panels (C) and (D) are based on the put...
Prevalence of mutations identified in clusters by phylogenetic analysis of 251 sequences with drug r...
<p><i>N</i>, number of individuals sequenced; VS, variable sites; PIS, parsimony information sites; ...
BACKGROUND: The distribution of human disease-associated mutations is not random across the human ge...
<p>(A) Mutation prevalences across time series. (B) One of 51 recombination networks that fit the da...
Comparing chromosomal gene order in two or more related species is an important approach to studying...
<p>The maximum likelihood phylogeny derived from a codon alignment of ‘core’ protein coding sequence...
<p>A) Chromosome 5 near <i>TMEM161B</i> and <i>MEF2C</i>, B) Chromosome 17 on <i>SFRS2</i> and C) Ch...
<p>The maximum likelihood phylogeny was inferred from the concatenated protein alignment of 2,374 si...
<p>For each locus (<i>FRI</i> [A], <i>Rpm1</i> [B], <i>Rps2</i> [C], and <i>Rps5</i> [D]), the botto...
<div><h3>Background</h3><p>The distribution of human disease-associated mutations is not random acro...
<p>The x-axis represents geographic locations where the isolates were collected. The y-axis represen...
<p>The concordance was based on the proportion of genomes in a cgMLST cluster that belonged to the p...
<p>Twelve representative CCGs are shown in (A) PCA plot where principle component analysis (PCA) of ...
<p>The proportion of closely related sequences in each of the five clusters shown in <a href="http:/...