Suppr超能文献

纳米形式:一个集成服务器,用于处理、分析和组装来自牛津纳米孔技术的微生物基因组原始测序数据。

NanoForms: an integrated server for processing, analysis and assembly of raw sequencing data of microbial genomes, from Oxford Nanopore technology.

作者信息

Czmil Anna, Wronski Michal, Czmil Sylwester, Sochacka-Pietal Marta, Cmil Michal, Gawor Jan, Wołkowicz Tomasz, Plewczynski Dariusz, Strzalka Dominik, Pietal Michal

机构信息

Department of Complex Systems, Rzeszow University of Technology, Rzeszow, Subcarpathian, Poland.

Department of Biotechnology and Bioinformatics, Rzeszow University of Technology, Rzeszow, Subcarpathian, Poland.

出版信息

PeerJ. 2022 Mar 29;10:e13056. doi: 10.7717/peerj.13056. eCollection 2022.

Abstract

BACKGROUND

Next Generation Sequencing (NGS) techniques dominate today's landscape of genetics and genomics research. Though Illumina still dominates worldwide sequencing, Oxford Nanopore is one of the leading technologies currently being used by biologists, medics and geneticists across various applications. Oxford Nanopore is automated and relatively simple for conducting experiments, but generates gigabytes of raw data, to be processed by often ambiguous set of alternative bioinformatics command-line tools, and genomics frameworks which require a knowledge of bioinformatics to run.

RESULTS

We established an inter-collegiate collaboration across experimentalists and bioinformaticians in order to provide a novel bioinformatics tool, free for academics. This tool allows people without extensive bioinformatics knowledge to simply process their raw genome sequencing data. Currently, due to ICT resources' maintenance reasons, our server is only capable of handling small genomes (up to 15 Mb). In this paper, we introduce our tool, NanoForms: an intuitive and integrated web server for the processing and analysis of raw prokaryotic genome data, coming from Oxford Nanopore. NanoForms is freely available for academics at the following locations: http://nanoforms.tech (webserver) and https://github.com/czmilanna/nanoforms (GitHub source repository).

摘要

背景

下一代测序(NGS)技术主导着当今的遗传学和基因组学研究领域。尽管Illumina在全球测序市场仍占据主导地位,但牛津纳米孔技术是目前生物学家、医学工作者和遗传学家在各种应用中使用的领先技术之一。牛津纳米孔技术实现了自动化,实验操作相对简单,但会生成数千兆字节的原始数据,需要由一系列常常模糊不清的替代生物信息学命令行工具以及需要生物信息学知识才能运行的基因组学框架来处理。

结果

我们在实验人员和生物信息学家之间建立了校际合作,以提供一种免费供学者使用的新型生物信息学工具。该工具使没有丰富生物信息学知识的人也能简单地处理他们的原始基因组测序数据。目前,由于信息通信技术资源维护的原因,我们的服务器仅能处理小基因组(最大15兆碱基)。在本文中,我们介绍我们的工具NanoForms:一个直观且集成的网络服务器,用于处理和分析来自牛津纳米孔技术的原核生物基因组原始数据。NanoForms可供学者免费使用,网址如下:http://nanoforms.tech(网络服务器)和https://github.com/czmilanna/nanoforms(GitHub源代码库)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8915/8973472/c01d9f14c000/peerj-10-13056-g001.jpg

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