pVACview: an interactive visualization tool for efficient neoantigen prioritization and selection

Huiming Xia, My Hoang, Evelyn Schmidt, Susanna Kiwala, Joshua McMichael, Zachary L. Skidmore, Bryan Fisk, Jonathan J. Song, Jasreet Hundal, Thomas Mooney, Jason R. Walker, S. Peter Goedegebuure, Christopher A. Miller, William E. Gillanders, Obi L. Griffith, Malachi Griffith
{"title":"pVACview: an interactive visualization tool for efficient neoantigen prioritization and selection","authors":"Huiming Xia, My Hoang, Evelyn Schmidt, Susanna Kiwala, Joshua McMichael, Zachary L. Skidmore, Bryan Fisk, Jonathan J. Song, Jasreet Hundal, Thomas Mooney, Jason R. Walker, S. Peter Goedegebuure, Christopher A. Miller, William E. Gillanders, Obi L. Griffith, Malachi Griffith","doi":"arxiv-2406.06985","DOIUrl":null,"url":null,"abstract":"Neoantigen targeting therapies including personalized vaccines have shown\npromise in the treatment of cancers. Accurate identification/prioritization of\nneoantigens is highly relevant to designing clinical trials, predicting\ntreatment response, and understanding mechanisms of resistance. With the advent\nof massively parallel sequencing technologies, it is now possible to predict\nneoantigens based on patient-specific variant information. However, numerous\nfactors must be considered when prioritizing neoantigens for use in\npersonalized therapies. Complexities such as alternative transcript\nannotations, various binding, presentation and immunogenicity prediction\nalgorithms, and variable peptide lengths/registers all potentially impact the\nneoantigen selection process. While computational tools generate numerous\nalgorithmic predictions for neoantigen characterization, results from these\npipelines are difficult to navigate and require extensive knowledge of the\nunderlying tools for accurate interpretation. Due to the intricate nature and\nnumber of salient neoantigen features, presenting all relevant information to\nfacilitate candidate selection for downstream applications is a difficult\nchallenge that current tools fail to address. We have created pVACview, the\nfirst interactive tool designed to aid in the prioritization and selection of\nneoantigen candidates for personalized neoantigen therapies. pVACview has a\nuser-friendly and intuitive interface where users can upload, explore, select\nand export their neoantigen candidates. The tool allows users to visualize\ncandidates using variant, transcript and peptide information. pVACview will\nallow researchers to analyze and prioritize neoantigen candidates with greater\nefficiency and accuracy in basic and translational settings. The application is\navailable as part of the pVACtools pipeline at pvactools.org and as an online\nserver at pvacview.org.","PeriodicalId":501070,"journal":{"name":"arXiv - QuanBio - Genomics","volume":"19 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Genomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2406.06985","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Neoantigen targeting therapies including personalized vaccines have shown promise in the treatment of cancers. Accurate identification/prioritization of neoantigens is highly relevant to designing clinical trials, predicting treatment response, and understanding mechanisms of resistance. With the advent of massively parallel sequencing technologies, it is now possible to predict neoantigens based on patient-specific variant information. However, numerous factors must be considered when prioritizing neoantigens for use in personalized therapies. Complexities such as alternative transcript annotations, various binding, presentation and immunogenicity prediction algorithms, and variable peptide lengths/registers all potentially impact the neoantigen selection process. While computational tools generate numerous algorithmic predictions for neoantigen characterization, results from these pipelines are difficult to navigate and require extensive knowledge of the underlying tools for accurate interpretation. Due to the intricate nature and number of salient neoantigen features, presenting all relevant information to facilitate candidate selection for downstream applications is a difficult challenge that current tools fail to address. We have created pVACview, the first interactive tool designed to aid in the prioritization and selection of neoantigen candidates for personalized neoantigen therapies. pVACview has a user-friendly and intuitive interface where users can upload, explore, select and export their neoantigen candidates. The tool allows users to visualize candidates using variant, transcript and peptide information. pVACview will allow researchers to analyze and prioritize neoantigen candidates with greater efficiency and accuracy in basic and translational settings. The application is available as part of the pVACtools pipeline at pvactools.org and as an online server at pvacview.org.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
pVACview:高效新抗原优先排序和选择的交互式可视化工具
包括个性化疫苗在内的新抗原靶向疗法在治疗癌症方面大有可为。准确识别/优先选择新抗原与设计临床试验、预测治疗反应和了解抗药性机制密切相关。随着大规模并行测序技术的发展,根据患者特异性变异信息预测内抗原已成为可能。然而,在确定用于个体化疗法的新抗原的优先级时,必须考虑许多因素。替代转录本注释、各种结合、表达和免疫原性预测算法以及可变的肽长度/序列等复杂因素都可能影响新抗原的选择过程。虽然计算工具能生成大量用于新抗原特征描述的算法预测结果,但这些管道产生的结果难以驾驭,需要对基础工具有广泛的了解才能准确解读。由于新抗原特征错综复杂且数量众多,如何呈现所有相关信息以方便下游应用的候选筛选是一个艰巨的挑战,而目前的工具无法解决这一问题。我们创建了 pVACview,这是第一款交互式工具,旨在帮助确定个性化新抗原疗法的新抗原候选物的优先级并进行筛选。该工具允许用户使用变体、转录本和肽信息对候选基因进行可视化处理。pVACview 将允许研究人员在基础和转化环境中高效、准确地分析和优先处理新抗原候选基因。该应用程序可作为 pVACtools pipeline 的一部分在 pvactools.org 上使用,也可作为在线服务器在 pvacview.org 上使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Allium Vegetables Intake and Digestive System Cancer Risk: A Study Based on Mendelian Randomization, Network Pharmacology and Molecular Docking wgatools: an ultrafast toolkit for manipulating whole genome alignments Selecting Differential Splicing Methods: Practical Considerations Advancements in colored k-mer sets: essentials for the curious Advancements in practical k-mer sets: essentials for the curious
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1