Semi-Automated Library Preparation for High-Throughput DNA Sequencing Platforms

Author:

Farias-Hesson Eveline1,Erikson Jonathan1,Atkins Alexander1,Shen Peidong2,Davis Ronald W.2,Scharfe Curt2,Pourmand Nader1

Affiliation:

1. Department of Biomolecular Engineering, University of California, 1156 High Street, Santa Cruz, CA 95064, USA

2. Stanford GenomeTechnology Center, Stanford University, 855 S. California Avenue, Palo Alto, CA 94304, USA

Abstract

Next-generation sequencing platforms are powerful technologies, providing gigabases of genetic information in a single run. An important prerequisite for high-throughput DNA sequencing is the development of robust and cost-effective preprocessing protocols for DNA sample library construction. Here we report the development of a semi-automated sample preparation protocol to produce adaptor-ligated fragment libraries. Using a liquid-handling robot in conjunction with Carboxy Terminated Magnetic Beads, we labeled each library sample using a unique 6 bp DNA barcode, which allowed multiplex sample processing and sequencing of 32 libraries in a single run using Applied Biosystems' SOLiD sequencer. We applied our semi-automated pipeline to targeted medical resequencing of nuclear candidate genes in individuals affected by mitochondrial disorders. This novel method is capable of preparing as much as 32 DNA libraries in 2.01 days (8-hour workday) for emulsion PCR/high throughput DNA sequencing, increasing sample preparation production by 8-fold.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology,Molecular Medicine,General Medicine,Biotechnology

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