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INSPIIRED:一种用于细胞基因组中新DNA整合位点定量分析的流程

INSPIIRED: A Pipeline for Quantitative Analysis of Sites of New DNA Integration in Cellular Genomes.

作者信息

Sherman Eric, Nobles Christopher, Berry Charles C, Six Emmanuelle, Wu Yinghua, Dryga Anatoly, Malani Nirav, Male Frances, Reddy Shantan, Bailey Aubrey, Bittinger Kyle, Everett John K, Caccavelli Laure, Drake Mary J, Bates Paul, Hacein-Bey-Abina Salima, Cavazzana Marina, Bushman Frederic D

机构信息

Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104-6076, USA.

Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, CA 92093, USA.

出版信息

Mol Ther Methods Clin Dev. 2016 Dec 18;4:39-49. doi: 10.1016/j.omtm.2016.11.002. eCollection 2017 Mar 17.

Abstract

Integration of new DNA into cellular genomes mediates replication of retroviruses and transposons; integration reactions have also been adapted for use in human gene therapy. Tracking the distributions of integration sites is important to characterize populations of transduced cells and to monitor potential outgrow of pathogenic cell clones. Here, we describe a pipeline for quantitative analysis of integration site distributions named INSPIIRED (integration site pipeline for paired-end reads). We describe optimized biochemical steps for site isolation using Illumina paired-end sequencing, including new technology for suppressing recovery of unwanted contaminants, then software for alignment, quality control, and management of integration site sequences. During library preparation, DNAs are broken by sonication, so that after ligation-mediated PCR the number of ligation junction sites can be used to infer abundance of gene-modified cells. We generated integration sites of known positions in silico, and we describe optimization of sample processing parameters refined by comparison to truth. We also present a novel graph-theory-based method for quantifying integration sites in repeated sequences, and we characterize the consequences using synthetic and experimental data. In an accompanying paper, we describe an additional set of statistical tools for data analysis and visualization. Software is available at https://github.com/BushmanLab/INSPIIRED.

摘要

新DNA整合到细胞基因组中介导逆转录病毒和转座子的复制;整合反应也已被应用于人类基因治疗。追踪整合位点的分布对于表征转导细胞群体以及监测致病细胞克隆的潜在增殖很重要。在这里,我们描述了一种用于整合位点分布定量分析的流程,称为INSPIIRED(双端读段整合位点流程)。我们描述了使用Illumina双端测序进行位点分离的优化生化步骤,包括抑制不需要的污染物回收的新技术,以及用于比对、质量控制和整合位点序列管理的软件。在文库制备过程中,DNA通过超声破碎,以便在连接介导的PCR后,连接连接位点的数量可用于推断基因修饰细胞的丰度。我们在计算机上生成了已知位置的整合位点,并描述了通过与真实情况比较而优化的样本处理参数。我们还提出了一种基于图论的新方法来量化重复序列中的整合位点,并使用合成数据和实验数据表征其结果。在一篇配套论文中,我们描述了另一组用于数据分析和可视化的统计工具。软件可在https://github.com/BushmanLab/INSPIIRED获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90ab/5363316/9379a88752a8/gr1.jpg

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