Reference is the consensus sequence of the inoculum and minority represents the polymorphic base at each site. Nucleotide variation was not detected in inoculum 2A and 3B1-3 coding regions. Sample count indicates the number of sample consensus sequences (of 52 total) that encoded each nucleotide found at the minority (2–49%) level in the inoculum deep sequence. Animal count indicates the number of individual hosts that provided sequences with these variants of the 13 total. If no value is indicated (-), no sample sequence encoded the inoculum’s minority nucleotide at the consensus level. Roman numerals and colors indicate the presence of each specific site change in at least one clade member as described in Results: Phylogenetic Association...
Comparison of the pattern of synonymous nucleotide substitution between two complete genomes of Myco...
<p>h haplotypes</p><p>Hd haplotype diversity</p><p>k average number of nucleotide differences</p><p>...
(A) Phylogenetic inconsistency between individual single nucleotide variants (SNVs) and core-genome-...
Contact tracing requires reliable identification of closely related bacterial isolates. When we noti...
<p>The scale bar represents one nucleotide substitution. <b>B) Frequency of each inoculum variant at...
<p>The consensus sequence for each unpassaged parent sample was compared to its passaged descendants...
Contact tracing requires reliable identification of closely related bacterial isolates. When we noti...
<p>All estimates were done after excluding homopolymer sites (HPs) from virus sequenced in 454.</p><...
<p>Nucleotide variants called in sample 178-3 relative to ancestral 178-2 genome 97 d post-sampling—...
Contact tracing requires reliable identification of closely related bacterial isolates. When we noti...
High-throughput sequencing such as those provided by Illumina are an efficient way to understand seq...
AbstractThe study of DNA sequence variation has been transformed by recent advances in DNA sequencin...
<p>Numbers in the second top correspond to the nucleotide positions under which the B95-8 prototype ...
<p>Frequency of consensus sequence containing the most abundant dinucleotide (a) and trinucleotide (...
Numerous sequencing projects have unveiled partial and full microbial genomes. The data produced far...
Comparison of the pattern of synonymous nucleotide substitution between two complete genomes of Myco...
<p>h haplotypes</p><p>Hd haplotype diversity</p><p>k average number of nucleotide differences</p><p>...
(A) Phylogenetic inconsistency between individual single nucleotide variants (SNVs) and core-genome-...
Contact tracing requires reliable identification of closely related bacterial isolates. When we noti...
<p>The scale bar represents one nucleotide substitution. <b>B) Frequency of each inoculum variant at...
<p>The consensus sequence for each unpassaged parent sample was compared to its passaged descendants...
Contact tracing requires reliable identification of closely related bacterial isolates. When we noti...
<p>All estimates were done after excluding homopolymer sites (HPs) from virus sequenced in 454.</p><...
<p>Nucleotide variants called in sample 178-3 relative to ancestral 178-2 genome 97 d post-sampling—...
Contact tracing requires reliable identification of closely related bacterial isolates. When we noti...
High-throughput sequencing such as those provided by Illumina are an efficient way to understand seq...
AbstractThe study of DNA sequence variation has been transformed by recent advances in DNA sequencin...
<p>Numbers in the second top correspond to the nucleotide positions under which the B95-8 prototype ...
<p>Frequency of consensus sequence containing the most abundant dinucleotide (a) and trinucleotide (...
Numerous sequencing projects have unveiled partial and full microbial genomes. The data produced far...
Comparison of the pattern of synonymous nucleotide substitution between two complete genomes of Myco...
<p>h haplotypes</p><p>Hd haplotype diversity</p><p>k average number of nucleotide differences</p><p>...
(A) Phylogenetic inconsistency between individual single nucleotide variants (SNVs) and core-genome-...