Evidence map›Paper›PMID 36434502›Full record

ArticleBMC bioinformatics2022

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

Chengyang Ji, Na Han, Yexiao Cheng, Jingzhe Shang, Shenghui Weng, Rong Yang, Hang-Yu Zhou, Aiping Wu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Chengyang JiInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China.
Na HanInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China.
Yexiao ChengInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China.
Jingzhe ShangInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China.
Shenghui WengInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China.
Rong YangInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China.
Hang-Yu ZhouInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China. zhy@ism.cams.cn.
Aiping WuInstitute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100005, China. wap@ism.cams.cn.ORCID http://orcid.org/0000-0002-5869-651X

Funding

CAMS Innovation Fund for Medical Sciences 2021-I2M-1-061China postdoctoral science foundation grants 2019M660548China postdoctoral science foundation grants 2020T130007ZXNational key research and development program 2021YFC230130National Natural Science Foundation of China 92169106Natural Science Foundation of Jiangsu Province BK20220278special research fund for central universities, Peking Union Medical College 2021-PT180-001Suzhou science and technology development plan szs2020311Youthful Teacher Project of Peking Union Medical College 3332019114
6 · The paper itself

Abstract

backgroundIdentifying 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.

resultsHere, 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.

conclusionsThe 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.

Indexed as

Influenza A Virus, H3N2 SubtypeInfluenza, HumanHumansMutationPhylogenyPolymorphism, GeneticSoftwarePhylogeneticsSequence analysisVisualization

Identifiers

PMID36434502
PMCPMC9701067

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.