Dataset Information

SitePath: a visual tool to identify polymorphism clades and help find fixed and parallel mutations.

ABSTRACT:

Background

Identifying polymorphism clades on phylogenetic trees could help detect punctual mutations that are associated with viral functions. With visualization tools coloring the tree, it is easy to visually find clades where most sequences have the same polymorphism state. However, with the fast accumulation of viral sequences, a computational tool to automate this process is urgently needed.

Results

Here, by implementing a branch-and-bound-like search method, we developed an R package named sitePath to identify polymorphism clades automatically. Based on the identified polymorphism clades, fixed and parallel mutations could be inferred. Furthermore, sitePath also integrated visualization tools to generate figures of the calculated results. In an example with the influenza A virus H3N2 dataset, the detected fixed mutations coincide with antigenic shift mutations. The highly specificity and sensitivity of sitePath in finding fixed mutations were achieved for a range of parameters and different phylogenetic tree inference software.

Conclusions

The result suggests that sitePath can identify polymorphism clades per site. The clustering of sequences on a phylogenetic tree can be used to infer fixed and parallel mutations. High-quality figures of the calculated results could also be generated by sitePath.

SUBMITTER: Ji C

PROVIDER: S-EPMC9701067 | biostudies-literature | 2022 Nov

REPOSITORIES: biostudies-literature

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Publications

sitePath: a visual tool to identify polymorphism clades and help find fixed and parallel mutations.

Ji Chengyang C Han Na N Cheng Yexiao Y Shang Jingzhe J Weng Shenghui S Yang Rong R Zhou Hang-Yu HY Wu Aiping A

BMC bioinformatics 20221124 1

<h4>Background</h4>Identifying polymorphism clades on phylogenetic trees could help detect punctual mutations that are associated with viral functions. With visualization tools coloring the tree, it is easy to visually find clades where most sequences have the same polymorphism state. However, with the fast accumulation of viral sequences, a computational tool to automate this process is urgently needed.<h4>Results</h4>Here, by implementing a branch-and-bound-like search method, we developed an ...[more]

PMID: 36434502

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