• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

VIRMOTIF:一个用于病毒序列分析的用户友好工具。

VIRMOTIF: A User-Friendly Tool for Viral Sequence Analysis.

机构信息

Amirkabir University of Technology, Tehran 346512, Iran.

AI-enabled Processes (AIP) Research Centre, Health Data Analytics Program, Macquarie University, Sydney, NSW 2109, Australia.

出版信息

Genes (Basel). 2021 Jan 27;12(2):186. doi: 10.3390/genes12020186.

DOI:10.3390/genes12020186
PMID:33514039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7911170/
Abstract

Bioinformatics and computational biology have significantly contributed to the generation of vast and important knowledge that can lead to great improvements and advancements in biology and its related fields. Over the past three decades, a wide range of tools and methods have been developed and proposed to enhance performance, diagnosis, and throughput while maintaining feasibility and convenience for users. Here, we propose a new user-friendly comprehensive tool called VIRMOTIF to analyze DNA sequences. VIRMOTIF brings different tools together as one package so that users can perform their analysis as a whole and in one place. VIRMOTIF is able to complete different tasks, including computing the number or probability of motifs appearing in DNA sequences, visualizing data using the matplotlib and heatmap libraries, and clustering data using four different methods, namely K-means, PCA, Mean Shift, and ClusterMap. VIRMOTIF is the only tool with the ability to analyze genomic motifs based on their frequency and representation (D-ratio) in a virus genome.

摘要

生物信息学和计算生物学为生成大量重要知识做出了重大贡献,这些知识可以为生物学及其相关领域带来巨大的改进和进步。在过去的三十年中,已经开发和提出了广泛的工具和方法,以提高性能、诊断和吞吐量,同时保持用户的可行性和便利性。在这里,我们提出了一个名为 VIRMOTIF 的新的用户友好型综合工具,用于分析 DNA 序列。VIRMOTIF 将不同的工具集成在一起作为一个包,以便用户可以整体地在一个地方进行分析。VIRMOTIF 能够完成不同的任务,包括计算 DNA 序列中出现的基序的数量或概率,使用 matplotlib 和 heatmap 库可视化数据,以及使用四种不同的方法(K-means、PCA、Mean Shift 和 ClusterMap)对数据进行聚类。VIRMOTIF 是唯一能够根据病毒基因组中基序的频率和表示(D-比)分析基因组基序的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/966ea0cb8881/genes-12-00186-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/55f4ebfb7228/genes-12-00186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/576fa0180a90/genes-12-00186-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/2773ea146ddd/genes-12-00186-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/985f480858ce/genes-12-00186-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/3a4847e7f555/genes-12-00186-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/966ea0cb8881/genes-12-00186-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/55f4ebfb7228/genes-12-00186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/576fa0180a90/genes-12-00186-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/2773ea146ddd/genes-12-00186-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/985f480858ce/genes-12-00186-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/3a4847e7f555/genes-12-00186-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd87/7911170/966ea0cb8881/genes-12-00186-g006.jpg

相似文献

1
VIRMOTIF: A User-Friendly Tool for Viral Sequence Analysis.VIRMOTIF:一个用于病毒序列分析的用户友好工具。
Genes (Basel). 2021 Jan 27;12(2):186. doi: 10.3390/genes12020186.
2
CLIMP: Clustering Motifs via Maximal Cliques with Parallel Computing Design.CLIMP:通过具有并行计算设计的最大团进行基序聚类
PLoS One. 2016 Aug 3;11(8):e0160435. doi: 10.1371/journal.pone.0160435. eCollection 2016.
3
ESAP plus: a web-based server for EST-SSR marker development.ESAP plus:一个用于EST-SSR标记开发的基于网络的服务器。
BMC Genomics. 2016 Dec 22;17(Suppl 13):1035. doi: 10.1186/s12864-016-3328-4.
4
The Genome Sequencer FLX System--longer reads, more applications, straight forward bioinformatics and more complete data sets.基因组测序仪FLX系统——读长更长、应用更多、生物信息学简单直接且数据集更完整。
J Biotechnol. 2008 Aug 31;136(1-2):3-10. doi: 10.1016/j.jbiotec.2008.03.021. Epub 2008 Jun 21.
5
Using SCOPE to identify potential regulatory motifs in coregulated genes.使用SCOPE鉴定共调控基因中的潜在调控基序。
J Vis Exp. 2011 May 31(51):2703. doi: 10.3791/2703.
6
Centroid based clustering of high throughput sequencing reads based on n-mer counts.基于 n -mer 计数的高通量测序reads 的质心聚类。
BMC Bioinformatics. 2013 Sep 8;14:268. doi: 10.1186/1471-2105-14-268.
7
SS-Wrapper: a package of wrapper applications for similarity searches on Linux clusters.SS-Wrapper:用于在Linux集群上进行相似性搜索的一组包装应用程序。
BMC Bioinformatics. 2004 Oct 28;5:171. doi: 10.1186/1471-2105-5-171.
8
DiffLogo: a comparative visualization of sequence motifs.DiffLogo:序列基序的比较可视化工具
BMC Bioinformatics. 2015 Nov 17;16:387. doi: 10.1186/s12859-015-0767-x.
9
PRECISE: software for prediction of cis-acting regulatory elements.PRECISE:用于预测顺式作用调控元件的软件。
J Hered. 2005 Sep-Oct;96(5):618-22. doi: 10.1093/jhered/esi094. Epub 2005 Aug 31.
10
GeneSpy, a user-friendly and flexible genomic context visualizer.基因间谍,一个用户友好且灵活的基因组上下文可视化工具。
Bioinformatics. 2019 Jan 15;35(2):329-331. doi: 10.1093/bioinformatics/bty459.

引用本文的文献

1
Phage quest: a beginner's guide to explore viral diversity in the prokaryotic world.噬菌体探索:探索原核生物世界中病毒多样性的初学者指南。
Brief Bioinform. 2025 Aug 31;26(5). doi: 10.1093/bib/bbaf449.
2
Proposing a hybrid technique of feature fusion and convolutional neural network for melanoma skin cancer detection.提出一种用于黑色素瘤皮肤癌检测的特征融合与卷积神经网络的混合技术。
J Pathol Inform. 2023 Oct 13;14:100341. doi: 10.1016/j.jpi.2023.100341. eCollection 2023.
3
A Comprehensive Investigation of Genomic Variants in Prostate Cancer Reveals 30 Putative Regulatory Variants.

本文引用的文献

1
A review on deep learning approaches in healthcare systems: Taxonomies, challenges, and open issues.深度学习在医疗系统中的应用综述:分类法、挑战和未解决的问题。
J Biomed Inform. 2021 Jan;113:103627. doi: 10.1016/j.jbi.2020.103627. Epub 2020 Nov 28.
2
CANCERSIGN: a user-friendly and robust tool for identification and classification of mutational signatures and patterns in cancer genomes.CANCERSIGN:一款用户友好且强大的工具,用于鉴定和分类癌症基因组中的突变特征和模式。
Sci Rep. 2020 Jan 28;10(1):1286. doi: 10.1038/s41598-020-58107-2.
3
The Immune Epitope Database and Analysis Resource in Epitope Discovery and Synthetic Vaccine Design.
全面研究前列腺癌的基因组变异揭示了 30 个潜在的调控变异。
Int J Mol Sci. 2023 Jan 27;24(3):2472. doi: 10.3390/ijms24032472.
4
MStoCIRC: A powerful tool for downstream analysis of MS/MS data to predict translatable circRNAs.MStoCIRC:用于对串联质谱数据进行下游分析以预测可翻译环状RNA的强大工具。
Front Mol Biosci. 2022 Aug 22;9:791797. doi: 10.3389/fmolb.2022.791797. eCollection 2022.
5
A Survey on Machine Learning and Internet of Medical Things-Based Approaches for Handling COVID-19: Meta-Analysis.基于机器学习和医疗物联网的 COVID-19 处理方法研究综述:荟萃分析。
Front Public Health. 2022 Jun 23;10:869238. doi: 10.3389/fpubh.2022.869238. eCollection 2022.
6
Is There a Need for a More Precise Description of Biomolecule Interactions to Understand Cell Function?是否需要对生物分子相互作用进行更精确的描述以理解细胞功能?
Curr Issues Mol Biol. 2022 Jan 21;44(2):505-525. doi: 10.3390/cimb44020035.
7
Hybrid HCNN-KNN Model Enhances Age Estimation Accuracy in Orthopantomography.混合 HCNN-KNN 模型提高了口腔全景片中的年龄估计准确性。
Front Public Health. 2022 May 30;10:879418. doi: 10.3389/fpubh.2022.879418. eCollection 2022.
8
Somatic point mutations are enriched in non-coding RNAs with possible regulatory function in breast cancer.体细胞点突变在非编码 RNA 中富集,这些非编码 RNA 可能在乳腺癌中具有调节功能。
Commun Biol. 2022 Jun 7;5(1):556. doi: 10.1038/s42003-022-03528-0.
9
Four-layer ConvNet to facial emotion recognition with minimal epochs and the significance of data diversity.四层卷积神经网络,使用最少的 epoch 进行面部情绪识别,以及数据多样性的重要性。
Sci Rep. 2022 Apr 28;12(1):6991. doi: 10.1038/s41598-022-11173-0.
10
Integrative analysis of mutated genes and mutational processes reveals novel mutational biomarkers in colorectal cancer.综合突变基因和突变过程分析揭示结直肠癌中的新型突变生物标志物。
BMC Bioinformatics. 2022 Apr 19;23(1):138. doi: 10.1186/s12859-022-04652-8.
免疫表位数据库与分析资源在表位发现及合成疫苗设计中的应用
Front Immunol. 2017 Mar 14;8:278. doi: 10.3389/fimmu.2017.00278. eCollection 2017.
4
Source of CpG Depletion in the HIV-1 Genome.HIV-1 基因组中 CpG 损耗的来源。
Mol Biol Evol. 2016 Dec;33(12):3205-3212. doi: 10.1093/molbev/msw205. Epub 2016 Sep 28.
5
High fidelity simian immunodeficiency virus reverse transcriptase mutants have impaired replication in vitro and in vivo.高保真猿猴免疫缺陷病毒逆转录酶突变体在体外和体内的复制均受损。
Virology. 2016 May;492:1-10. doi: 10.1016/j.virol.2016.02.008. Epub 2016 Feb 19.
6
Deep learning for regulatory genomics.用于调控基因组学的深度学习
Nat Biotechnol. 2015 Aug;33(8):825-6. doi: 10.1038/nbt.3313.
7
Machine learning applications in genetics and genomics.机器学习在遗传学和基因组学中的应用。
Nat Rev Genet. 2015 Jun;16(6):321-32. doi: 10.1038/nrg3920. Epub 2015 May 7.
8
Linking pig-tailed macaque major histocompatibility complex class I haplotypes and cytotoxic T lymphocyte escape mutations in simian immunodeficiency virus infection.将猪尾猕猴主要组织相容性复合体I类单倍型与猿猴免疫缺陷病毒感染中的细胞毒性T淋巴细胞逃逸突变联系起来。
J Virol. 2014 Dec;88(24):14310-25. doi: 10.1128/JVI.02428-14. Epub 2014 Oct 1.
9
Insights into the motif preference of APOBEC3 enzymes.APOBEC3 酶基序偏好的研究进展。
PLoS One. 2014 Jan 31;9(1):e87679. doi: 10.1371/journal.pone.0087679. eCollection 2014.
10
Signatures of mutational processes in human cancer.人类癌症中的突变过程特征。
Nature. 2013 Aug 22;500(7463):415-21. doi: 10.1038/nature12477. Epub 2013 Aug 14.