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参考序列浏览器:一个带有用户友好的图形界面的 R 应用程序,用于快速查询序列数据库。

Reference Sequence Browser: An R application with a user-friendly GUI to rapidly query sequence databases.

机构信息

Department of Computer Science and Engineering, University of California Santa Cruz, Santa Cruz, CA, United States of America.

Department of Ecology and Evolutionary Biology, University of California Santa Cruz, Santa Cruz, CA, United States of America.

出版信息

PLoS One. 2024 Oct 31;19(10):e0309707. doi: 10.1371/journal.pone.0309707. eCollection 2024.

Abstract

Land managers, researchers, and regulators increasingly utilize environmental DNA (eDNA) techniques to monitor species richness, presence, and absence. In order to properly develop a biological assay for eDNA metabarcoding or quantitative PCR, scientists must be able to find not only reference sequences (previously identified sequences in a genomics database) that match their target taxa but also reference sequences that match non-target taxa. Determining which taxa have publicly available sequences in a time-efficient and accurate manner currently requires computational skills to search, manipulate, and parse multiple unconnected DNA sequence databases. Our team iteratively designed a Graphic User Interface (GUI) Shiny application called the Reference Sequence Browser (RSB) that provides users efficient and intuitive access to multiple genetic databases regardless of computer programming expertise. The application returns the number of publicly accessible barcode markers per organism in the NCBI Nucleotide, BOLD, or CALeDNA CRUX Metabarcoding Reference Databases. Depending on the database, we offer various search filters such as min and max sequence length or country of origin. Users can then download the FASTA/GenBank files from the RSB web tool, view statistics about the data, and explore results to determine details about the availability or absence of reference sequences.

摘要

土地管理者、研究人员和监管机构越来越多地利用环境 DNA(eDNA)技术来监测物种丰富度、存在和缺失情况。为了正确开发用于 eDNA 宏条形码或定量 PCR 的生物测定法,科学家们不仅必须能够找到与其目标分类群匹配的参考序列(基因组学数据库中先前确定的序列),还必须找到与非目标分类群匹配的参考序列。目前,要以高效和准确的方式确定哪些分类群在公共数据库中有可用序列,需要具备搜索、操作和解析多个不相关的 DNA 序列数据库的计算技能。我们的团队反复设计了一个名为参考序列浏览器(RSB)的图形用户界面(GUI)Shiny 应用程序,该应用程序为用户提供了高效和直观的访问多个遗传数据库的途径,而无需具备计算机编程专业知识。该应用程序返回 NCBI Nucleotide、BOLD 或 CALeDNA CRUX Metabarcoding Reference Databases 中每个生物体的公开可访问条形码标记数量。根据数据库的不同,我们提供了各种搜索过滤器,例如最小和最大序列长度或原产国。然后,用户可以从 RSB 网络工具下载 FASTA/GenBank 文件,查看有关数据的统计信息,并探索结果以确定参考序列的可用性或缺失情况的详细信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f907/11527216/516b12736831/pone.0309707.g001.jpg

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