3D Printing-Enabled DNA Extraction for Long-Read Genomics

被引:7
作者
Agrawal, Paridhi [1 ]
Reifenberger, Jeffrey G. [2 ]
Dorfman, Kevin D. [1 ]
机构
[1] Univ Minnesota Twin Cities, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Bionano Genom Inc, San Diego, CA 92121 USA
关键词
HIGH-ASPECT-RATIO; STRUCTURAL VARIATION; CHROMOSOME; MOLECULES;
D O I
10.1021/acsomega.0c01912
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Long-read genomics technologies such as nanopore sequencing and genome mapping in nanochannels extract genomic information in the kilobase to megabase pair range from single DNA molecules, thereby overcoming read-length limitations in next-generation DNA sequencing. Long-read technologies start with long DNA molecules as the input and thus benefit from universal sample preparation methods that are fast and shear-free and present a scope of automation and direct upstream integration. We describe a 3D printing-assisted poly(dimethylysiloxane)-based DNA sample preparation device, where diffusive chemical lysis followed by electrophoresis produces circa 100 ng of long DNA directly from cells with less than 5 min of labor. Assessment of the product DNA by confinement in nanochannels reveals that the DNA sizes are commensurate with the requirements for long-read single-molecule technologies. Microfluidics not only expedites sample preparation, but also offers the opportunity for integration with genomics technologies to eliminate DNA fragmentation and loss during transfer to the genomic device.
引用
收藏
页码:20817 / 20824
页数:8
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