首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >Quality control of next-generation sequencing library through an integrative digital microfluidic platform
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Quality control of next-generation sequencing library through an integrative digital microfluidic platform

机译:通过集成的数字微流体平台进行下一代测序文库的质量控制

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We have developed an automated quality control (QC) platform for next-generation sequencing (NGS) library characterization by integrating a droplet-based digital microfluidic (DMF) system with a capillary-based reagent delivery unit and a quantitative CE module. Using an in-plane capillary-DMF interface, a prepared sample droplet was actuated into position between the ground electrode and the inlet of the separation capillary to complete the circuit for an electrokinetic injection. Using a DNA ladder as an internal standard, the CE module with a compact LIF detector was capable of detecting dsDNA in the range of 5-100 pg/??L, suitable for the amount of DNA required by the Illumina Genome Analyzer sequencing platform. This DMF-CE platform consumes tenfold less sample volume than the current Agilent BioAnalyzer QC technique, preserving precious sample while providing necessary sensitivity and accuracy for optimal sequencing performance. The ability of this microfluidic system to validate NGS library preparation was demonstrated by examining the effects of limited-cycle PCR amplification on the size distribution and the yield of Illumina-compatible libraries, demonstrating that as few as ten cycles of PCR bias the size distribution of the library toward undesirable larger fragments. ? 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
机译:通过将基于液滴的数字微流体(DMF)系统与基于毛细管的试剂输送单元和定量CE模块集成在一起,我们已经开发了用于下一代测序(NGS)库表征的自动化质量控制(QC)平台。使用面内毛细管-DMF接口,将准备好的样品液滴驱动到接地电极和分离毛细管入口之间的位置,以完成电动注入的电路。使用DNA阶梯作为内标,带有紧凑型LIF检测器的CE模块能够检测5-100 pg /ΔL的dsDNA,适合Illumina Genome Analyzer测序平台所需的DNA量。该DMF-CE平台消耗的样品量比当前的Agilent BioAnalyzer QC技术少十倍,从而保留了宝贵的样品,同时提供了必要的灵敏度和准确性,以实现最佳的测序性能。通过检查有限循环PCR扩增对Illumina兼容文库的大小分布和产量的影响,证明了这种微流体系统验证NGS文库制备能力的能力,这表明只有十个PCR循环会偏向PCR的大小分布。库中出现不需要的较大片段。 ? 2012 WILEY-VCH Verlag GmbH&Co.KGaA,魏因海姆。

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