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使用高通量测序生成的病毒插入位点数据的生物信息学分析质量指标的开发与评估

Development and Evaluation of Quality Metrics for Bioinformatics Analysis of Viral Insertion Site Data Generated Using High Throughput Sequencing.

作者信息

Gao Hongyu, Hawkins Troy, Jasti Aparna, Chen Yu-Hsiang, Mockaitis Keithanne, Dinauer Mary, Cornetta Kenneth

机构信息

Department of Medical and Molecular Genetics, Indiana University School of Medicine, IB 130, 975 West Walnut Street, Indianapolis, IN 46202, USA.

Department of Biology, Indiana University-Purdue University, Indianapolis, IN 46202, USA.

出版信息

Biomedicines. 2014 May 6;2(2):195-210. doi: 10.3390/biomedicines2020195.

Abstract

Integration of viral vectors into a host genome is associated with insertional mutagenesis and subjects in clinical gene therapy trials must be monitored for this adverse event. Several PCR based methods such as ligase-mediated (LM) PCR, linear-amplification-mediated (LAM) PCR and non-restrictive (nr) LAM PCR were developed to identify sites of vector integration. Coupling the power of next-generation sequencing technologies with various PCR approaches will provide a comprehensive and genome-wide profiling of insertion sites and increase throughput. In this bioinformatics study, we aimed to develop and apply quality metrics to viral insertion data obtained using next-generation sequencing. We developed five simple metrics for assessing next-generation sequencing data from different PCR products and showed how the metrics can be used to objectively compare runs performed with the same methodology as well as data generated using different PCR techniques. The results will help researchers troubleshoot complex methodologies, understand the quality of sequencing data, and provide a starting point for developing standardization of vector insertion site data analysis.

摘要

病毒载体整合到宿主基因组中与插入诱变有关,临床基因治疗试验中的受试者必须对此不良事件进行监测。已经开发了几种基于PCR的方法,如连接酶介导(LM)PCR、线性扩增介导(LAM)PCR和非限制性(nr)LAM PCR,以鉴定载体整合位点。将下一代测序技术的强大功能与各种PCR方法相结合,将提供插入位点的全面全基因组分析,并提高通量。在这项生物信息学研究中,我们旨在开发质量指标并将其应用于使用下一代测序获得的病毒插入数据。我们开发了五个简单的指标来评估来自不同PCR产物的下一代测序数据,并展示了这些指标如何用于客观比较使用相同方法进行的运行以及使用不同PCR技术生成的数据。这些结果将帮助研究人员解决复杂的方法问题,了解测序数据的质量,并为制定载体插入位点数据分析的标准化提供一个起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fe0/5423470/6abfb6e13346/biomedicines-02-00195-g001.jpg

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