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A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing

Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic information for a wide range of applications. Unfortunately, the surging popularity of NGS has not yet been accompanied by an improvement in automated techniques for preparing formatted sequencing libraries. To a...

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Autores principales: Kim, Hanyoup, Jebrail, Mais J., Sinha, Anupama, Bent, Zachary W., Solberg, Owen D., Williams, Kelly P., Langevin, Stanley A., Renzi, Ronald F., Van De Vreugde, James L., Meagher, Robert J., Schoeniger, Joseph S., Lane, Todd W., Branda, Steven S., Bartsch, Michael S., Patel, Kamlesh D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718812/
https://www.ncbi.nlm.nih.gov/pubmed/23894387
http://dx.doi.org/10.1371/journal.pone.0068988
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author Kim, Hanyoup
Jebrail, Mais J.
Sinha, Anupama
Bent, Zachary W.
Solberg, Owen D.
Williams, Kelly P.
Langevin, Stanley A.
Renzi, Ronald F.
Van De Vreugde, James L.
Meagher, Robert J.
Schoeniger, Joseph S.
Lane, Todd W.
Branda, Steven S.
Bartsch, Michael S.
Patel, Kamlesh D.
author_facet Kim, Hanyoup
Jebrail, Mais J.
Sinha, Anupama
Bent, Zachary W.
Solberg, Owen D.
Williams, Kelly P.
Langevin, Stanley A.
Renzi, Ronald F.
Van De Vreugde, James L.
Meagher, Robert J.
Schoeniger, Joseph S.
Lane, Todd W.
Branda, Steven S.
Bartsch, Michael S.
Patel, Kamlesh D.
author_sort Kim, Hanyoup
collection PubMed
description Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic information for a wide range of applications. Unfortunately, the surging popularity of NGS has not yet been accompanied by an improvement in automated techniques for preparing formatted sequencing libraries. To address this challenge, we have developed a prototype microfluidic system for preparing sequencer-ready DNA libraries for analysis by Illumina sequencing. Our system combines droplet-based digital microfluidic (DMF) sample handling with peripheral modules to create a fully-integrated, sample-in library-out platform. In this report, we use our automated system to prepare NGS libraries from samples of human and bacterial genomic DNA. E. coli libraries prepared on-device from 5 ng of total DNA yielded excellent sequence coverage over the entire bacterial genome, with >99% alignment to the reference genome, even genome coverage, and good quality scores. Furthermore, we produced a de novo assembly on a previously unsequenced multi-drug resistant Klebsiella pneumoniae strain BAA-2146 (KpnNDM). The new method described here is fast, robust, scalable, and automated. Our device for library preparation will assist in the integration of NGS technology into a wide variety of laboratories, including small research laboratories and clinical laboratories.
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spelling pubmed-37188122013-07-26 A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing Kim, Hanyoup Jebrail, Mais J. Sinha, Anupama Bent, Zachary W. Solberg, Owen D. Williams, Kelly P. Langevin, Stanley A. Renzi, Ronald F. Van De Vreugde, James L. Meagher, Robert J. Schoeniger, Joseph S. Lane, Todd W. Branda, Steven S. Bartsch, Michael S. Patel, Kamlesh D. PLoS One Research Article Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic information for a wide range of applications. Unfortunately, the surging popularity of NGS has not yet been accompanied by an improvement in automated techniques for preparing formatted sequencing libraries. To address this challenge, we have developed a prototype microfluidic system for preparing sequencer-ready DNA libraries for analysis by Illumina sequencing. Our system combines droplet-based digital microfluidic (DMF) sample handling with peripheral modules to create a fully-integrated, sample-in library-out platform. In this report, we use our automated system to prepare NGS libraries from samples of human and bacterial genomic DNA. E. coli libraries prepared on-device from 5 ng of total DNA yielded excellent sequence coverage over the entire bacterial genome, with >99% alignment to the reference genome, even genome coverage, and good quality scores. Furthermore, we produced a de novo assembly on a previously unsequenced multi-drug resistant Klebsiella pneumoniae strain BAA-2146 (KpnNDM). The new method described here is fast, robust, scalable, and automated. Our device for library preparation will assist in the integration of NGS technology into a wide variety of laboratories, including small research laboratories and clinical laboratories. Public Library of Science 2013-07-22 /pmc/articles/PMC3718812/ /pubmed/23894387 http://dx.doi.org/10.1371/journal.pone.0068988 Text en © 2013 Kim et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kim, Hanyoup
Jebrail, Mais J.
Sinha, Anupama
Bent, Zachary W.
Solberg, Owen D.
Williams, Kelly P.
Langevin, Stanley A.
Renzi, Ronald F.
Van De Vreugde, James L.
Meagher, Robert J.
Schoeniger, Joseph S.
Lane, Todd W.
Branda, Steven S.
Bartsch, Michael S.
Patel, Kamlesh D.
A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing
title A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing
title_full A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing
title_fullStr A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing
title_full_unstemmed A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing
title_short A Microfluidic DNA Library Preparation Platform for Next-Generation Sequencing
title_sort microfluidic dna library preparation platform for next-generation sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718812/
https://www.ncbi.nlm.nih.gov/pubmed/23894387
http://dx.doi.org/10.1371/journal.pone.0068988
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