Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Dec 14;12(12):1437. doi: 10.3390/v12121437

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2020 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

PMC Copyright notice

Phylogenetic trees and pairwise distance comparisons for novel lineages/sublineages of high-risk HPV complete genome variants. Phylogenetic trees were inferred from a global alignment of the complete genome nucleotide sequences of the variants from following HPV genotypes using RAxML: (A) HPV45, (B) HPV52, (C) HPV59, (D) HPV66. A star () indicates novel lineage/sublineage. The phylogenetic topology is shown on the left, pairwise differences for each isolate are shown on the right. Values for each isolate are connected by lines of different colors to distinguish each lineage and sublineage. Genomes from our collection are indicated with LNS identification number.

Phylogenetic trees and pairwise distance comparisons for novel lineages/sublineages of high-risk HPV complete genome variants. Phylogenetic trees were inferred from a global alignment of the complete genome nucleotide sequences of the variants from following HPV genotypes using RAxML: (A) HPV45, (B) HPV52, (C) HPV59, (D) HPV66. A star () indicates novel lineage/sublineage. The phylogenetic topology is shown on the left, pairwise differences for each isolate are shown on the right. Values for each isolate are connected by lines of different colors to distinguish each lineage and sublineage. Genomes from our collection are indicated with LNS identification number.