National Veterinary Services Laboratories (NVSL), USDA, 1920 Dayton Avenue, Ames, IA, 50010, USA.
BMC Genomics. 2024 Jun 1;25(1):545. doi: 10.1186/s12864-024-10437-5.
Several single nucleotide polymorphism (SNP) pipelines exist, each offering its own advantages. Among them and described here is vSNP that has been developed over the past decade and is specifically tailored to meet the needs of diagnostic laboratories. Laboratories that aim to provide rapid whole genome sequencing results during outbreak investigations face unique challenges. vSNP addresses these challenges by enabling users to verify and validate sequence accuracy with ease- having utility across various pathogens, being fully auditable, and presenting results that are easy to interpret and can be comprehended by individuals with diverse backgrounds.
vSNP has proven effective for real-time phylogenetic analysis of disease outbreaks and eradication efforts, including bovine tuberculosis, brucellosis, virulent Newcastle disease, SARS-CoV-2, African swine fever, and highly pathogenic avian influenza. The pipeline produces easy-to-read SNP matrices, sorted for convenience, as well as corresponding phylogenetic trees, making the output easily understandable. Essential data for verifying SNPs is included in the output, and the process has been divided into two steps for ease of use and faster processing times. vSNP requires minimal computational resources to run and can be run in a wide range of environments. Several utilities have been developed to make analysis more accessible for subject matter experts who may not have computational expertise.
The vSNP pipeline integrates seamlessly into a diagnostic workflow and meets the criteria for quality control accreditation programs, such as 17025 by the International Organization for Standardization. Its versatility and robustness make it suitable for use with a diverse range of organisms, providing detailed, reproducible, and transparent results, making it a valuable tool in various applications, including phylogenetic analysis performed in real time.
有几种单核苷酸多态性(SNP)分析工具,每种都有其自身的优势。在这些工具中,我们介绍了 vSNP,它是过去十年开发的,专门针对诊断实验室的需求进行了优化。在暴发调查中,旨在提供快速全基因组测序结果的实验室面临着独特的挑战。vSNP 通过使使用者能够轻松地验证和验证序列准确性来应对这些挑战——它在各种病原体中都具有实用性,完全可审计,并且提供的结果易于解释,并且可以被具有不同背景的人理解。
vSNP 已被证明可有效地用于实时分析疾病暴发和根除工作的系统发育,包括牛结核病、布鲁氏菌病、强毒新城疫、SARS-CoV-2、非洲猪瘟和高致病性禽流感。该分析工具生成易于阅读的 SNP 矩阵,按方便排序,并相应地提供系统发育树,使输出结果易于理解。输出结果中包含用于验证 SNP 的必要数据,并且该过程已分为两个步骤,以提高易用性和更快的处理时间。vSNP 运行所需的计算资源最少,可以在广泛的环境中运行。为了使不具备计算专业知识的主题专家更容易进行分析,已经开发了几种实用程序。
vSNP 分析工具无缝集成到诊断工作流程中,并符合质量控制认证计划的标准,例如国际标准化组织的 17025。其多功能性和稳健性使其适用于各种生物体,提供详细、可重复和透明的结果,使其成为各种应用的有价值的工具,包括实时进行的系统发育分析。