Ultra-fast sample-to-sequencing workflow for clinical diagnostics using micropillars
Adam J BisogniiD, Irem Bastuzel, Mohamed Z. RashediD, Joy GoffenaiD, Sophie H. R. StorziD, Zachary B. AndersoniD, Min Seon ParkiD, Trent M. PralliD, Miranda Pg Zalusky, Erin E. CrottyiD, Bonnie ColeiD, Jeffrey Stevens, David Ming LiniD, Harvey C. TianiD, Danny E. MilleriD
Abstract
We present a streamlined, solid-phase workflow for Oxford Nanopore sequencing that integrates DNA extraction, purification, and library preparation within a single microfluidic cartridge. By eliminating tube transfers and performing all enzymatic steps directly on captured DNA, the method minimizes sample loss, reduces hands-on time, and simplifies library generation for long-read sequencing. Starting from volumes as small as a single drop of blood, this integrated approach produces high-quality sequencing libraries from cell lines, whole blood, and tissue. The workflow achieves robust recovery of high-molecular-weight DNA and high pore occupancy, enabling rapid, low-complexity sample preparation suitable for clinical, field, and decentralized sequencing applications.
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