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利用液滴 MDA 进行纳米孔测序的超低输入基因组文库制备

Ultralow-Input Genome Library Preparation for Nanopore Sequencing with Droplet MDA.

机构信息

Institute for Advanced Biosciences, Keio University, Yamagata, Japan.

Graduate School of Media and Governance, Keio University, Fujisawa, Kanagawa, Japan.

出版信息

Methods Mol Biol. 2023;2632:91-100. doi: 10.1007/978-1-0716-2996-3_7.

Abstract

Genome sequencing of small species, such as those of meinofauna, can be challenging due to the extremely low input of genomic DNA. While nanopore sequencing is a promising technology for genome assembly due to its limitless long reads, recommended input of 1 μg for the Ligation Sequencing Kit often precludes the use of this technology. Here, I detail an unbiased droplet-based multiple displacement amplification of picogram order of DNA to realize nanopore sequencing with ultralow input of genomic DNA. For this purpose, a microfluidic chip of 10X Genomics Chromium Controller is utilized. With this method, over 10 μg of unbiased amplicons around 10 kbp in length can be obtained from as low as 50 μg of input DNA, which is enough for the construction of multiple sequencing libraries, or for the size selection of longer DNA fragments.

摘要

由于基因组 DNA 的极低输入量,小物种(如 meinofauna 等)的基因组测序可能具有挑战性。虽然纳米孔测序因其无限长的读长而成为基因组组装的一项有前途的技术,但 Ligation Sequencing Kit 的推荐输入量为 1μg,这通常排除了该技术的使用。在这里,我详细介绍了一种基于液滴的皮克数量级 DNA 的无偏分散式多次置换扩增,以实现超低输入量的基因组 DNA 的纳米孔测序。为此,使用了 10X Genomics Chromium Controller 的微流控芯片。通过这种方法,即使输入 DNA 低至 50μg,也可以获得超过 10μg 的无偏扩增子,长度约为 10 kbp,这足以构建多个测序文库,或对较长 DNA 片段进行大小选择。

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