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All-in-one sequencing: an improved library preparation method for cost-effective and high-throughput next-generation sequencing

机译:多合一测序:一种改进的文库制备方法用于具有成本效益的高通量下一代测序

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摘要

Flowchart for the All-in-One sequencing (AIO-seq) method. The libraries were prepared using Tn5 transposase. The process of mechanical fragmentation was used to prepare the libraries. In the traditional protocol, the size selection, and quantification were processed using a one sample one tube method. With the AIO-seq method, the library analyzed by the Agilent 2100 Bioanalyzer will give the fragment distribution pattern and the ratio of the target region (between the two blue lines) to the total library. The concentration of the total library could be obtained by Qubit™ 4.0 Fluorometer. The target region concentrations (TRC) were calculated within each library by multiplying the proportion of the target region from ( ) and the total library concentration from ( ). Mixing the libraries in one tube according to the calculated TRC and their expected yields of the sequence data. – One size selection by Sage HT. Quantification of the selected fragment by qPCR and sequencing
机译:多合一测序(AIO-seq)方法的流程图。使用Tn5转座酶制备文库。机械破碎过程用于制备文库。在传统方案中,使用单样本单管方法处理大小选择和定量。使用AIO-seq方法,由Agilent 2100生物分析仪分析的文库将给出片段分布图以及目标区域(两条蓝线之间)与总文库的比率。总库的浓度可以通过Qubit™4.0荧光计获得。通过将()中的目标区域比例与()中的总文库浓度相乘,可以计算出每个文库中的目标区域浓度(TRC)。根据计算出的TRC及其序列数据的预期产量,将文库混合在一个试管中。 – Sage HT选择一种尺寸。通过qPCR和测序对所选片段进行定量

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