Illumina, Inc., Madison, WI, USA.
Illumina, Inc., Great Abington, Cambridge, UK.
BMC Genomics. 2018 Oct 1;19(1):722. doi: 10.1186/s12864-018-5096-9.
Transposome-based technologies have enabled the streamlined production of sequencer-ready DNA libraries; however, current methods are highly sensitive to the amount and quality of input nucleic acid.
We describe a new library preparation technology (Nextera DNA Flex) that utilizes a known concentration of transposomes conjugated directly to beads to bind a fixed amount of DNA, and enables direct input of blood and saliva using an integrated extraction protocol. We further report results from libraries generated outside the standard parameters of the workflow, highlighting novel applications for Nextera DNA Flex, including human genome builds and variant calling from below 1 ng DNA input, customization of insert size, and preparation of libraries from short fragments and severely degraded FFPE samples. Using this bead-linked library preparation method, library yield saturation was observed at an input amount of 100 ng. Preparation of libraries from a range of species with varying GC levels demonstrated uniform coverage of small genomes. For large and complex genomes, coverage across the genome, including difficult regions, was improved compared with other library preparation methods. Libraries were successfully generated from amplicons of varying sizes (from 50 bp to 11 kb), however, a decrease in efficiency was observed for amplicons smaller than 250 bp. This library preparation method was also compatible with poor-quality DNA samples, with sequenceable libraries prepared from formalin-fixed paraffin-embedded samples with varying levels of degradation.
In contrast to solution-based library preparation, this bead-based technology produces a normalized, sequencing-ready library for a wide range of DNA input types and amounts, largely obviating the need for DNA quantitation. The robustness of this bead-based library preparation kit and flexibility of input DNA facilitates application across a wide range of fields.
转座子为基础的技术使高通量制备测序文库成为可能;然而,当前的方法对输入核酸的量和质量非常敏感。
我们描述了一种新的文库制备技术(Nextera DNA Flex),该技术利用已知浓度的转座酶直接连接到珠子上,结合固定量的 DNA,并通过集成的提取方案直接输入血液和唾液。我们进一步报告了在工作流程标准参数之外生成的文库的结果,突出了 Nextera DNA Flex 的新应用,包括来自低于 1ng DNA 输入的人类基因组构建和变体调用、插入大小的定制以及来自短片段和严重降解 FFPE 样品的文库制备。使用这种珠联式文库制备方法,在输入量为 100ng 时观察到文库产量饱和。用不同 GC 水平的各种物种制备文库,证明了小基因组的均匀覆盖。对于大而复杂的基因组,与其他文库制备方法相比,包括困难区域在内的整个基因组的覆盖得到了改善。成功地从不同大小(从 50bp 到 11kb)的扩增子制备了文库,然而,对于小于 250bp 的扩增子,效率降低。这种文库制备方法也与低质量的 DNA 样本兼容,可从福尔马林固定石蜡包埋的样本中制备可测序的文库,这些样本的降解程度不同。
与基于溶液的文库制备方法相比,这种基于珠子的技术为广泛的 DNA 输入类型和数量产生了归一化的、测序就绪的文库,在很大程度上避免了 DNA 定量的需要。这种基于珠子的文库制备试剂盒的稳健性和输入 DNA 的灵活性促进了在广泛领域的应用。