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Miniaturization and optimization of 384-well compatible RNA sequencing library preparation

Preparation of high-quality sequencing libraries is a costly and time-consuming component of metagenomic next generation sequencing (mNGS). While the overall cost of sequencing has dropped significantly over recent years, the reagents needed to prepare sequencing samples are likely to become the dom...

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Autores principales: Mayday, Madeline Y., Khan, Lillian M., Chow, Eric D., Zinter, Matt S., DeRisi, Joseph L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328170/
https://www.ncbi.nlm.nih.gov/pubmed/30629604
http://dx.doi.org/10.1371/journal.pone.0206194
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author Mayday, Madeline Y.
Khan, Lillian M.
Chow, Eric D.
Zinter, Matt S.
DeRisi, Joseph L.
author_facet Mayday, Madeline Y.
Khan, Lillian M.
Chow, Eric D.
Zinter, Matt S.
DeRisi, Joseph L.
author_sort Mayday, Madeline Y.
collection PubMed
description Preparation of high-quality sequencing libraries is a costly and time-consuming component of metagenomic next generation sequencing (mNGS). While the overall cost of sequencing has dropped significantly over recent years, the reagents needed to prepare sequencing samples are likely to become the dominant expense in the process. Furthermore, libraries prepared by hand are subject to human variability and needless waste due to limitations of manual pipetting volumes. Reduction of reaction volumes, combined with sub-microliter automated dispensing of reagents without consumable pipette tips, has the potential to provide significant advantages. Here, we describe the integration of several instruments, including the Labcyte Echo 525 acoustic liquid handler and the iSeq and NovaSeq Illumina sequencing platforms, to miniaturize and automate mNGS library preparation, significantly reducing the cost and the time required to prepare samples. Through the use of External RNA Controls Consortium (ERCC) spike-in RNAs, we demonstrated the fidelity of the miniaturized preparation to be equivalent to full volume reactions. Furthermore, detection of viral and microbial species from cell culture and patient samples was also maintained in the miniaturized libraries. For 384-well mNGS library preparations, we achieved cost savings of over 80% in materials and reagents alone, and reduced preparation time by 90% compared to manual approaches, without compromising quality or representation within the library.
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spelling pubmed-63281702019-02-01 Miniaturization and optimization of 384-well compatible RNA sequencing library preparation Mayday, Madeline Y. Khan, Lillian M. Chow, Eric D. Zinter, Matt S. DeRisi, Joseph L. PLoS One Research Article Preparation of high-quality sequencing libraries is a costly and time-consuming component of metagenomic next generation sequencing (mNGS). While the overall cost of sequencing has dropped significantly over recent years, the reagents needed to prepare sequencing samples are likely to become the dominant expense in the process. Furthermore, libraries prepared by hand are subject to human variability and needless waste due to limitations of manual pipetting volumes. Reduction of reaction volumes, combined with sub-microliter automated dispensing of reagents without consumable pipette tips, has the potential to provide significant advantages. Here, we describe the integration of several instruments, including the Labcyte Echo 525 acoustic liquid handler and the iSeq and NovaSeq Illumina sequencing platforms, to miniaturize and automate mNGS library preparation, significantly reducing the cost and the time required to prepare samples. Through the use of External RNA Controls Consortium (ERCC) spike-in RNAs, we demonstrated the fidelity of the miniaturized preparation to be equivalent to full volume reactions. Furthermore, detection of viral and microbial species from cell culture and patient samples was also maintained in the miniaturized libraries. For 384-well mNGS library preparations, we achieved cost savings of over 80% in materials and reagents alone, and reduced preparation time by 90% compared to manual approaches, without compromising quality or representation within the library. Public Library of Science 2019-01-10 /pmc/articles/PMC6328170/ /pubmed/30629604 http://dx.doi.org/10.1371/journal.pone.0206194 Text en © 2019 Mayday 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mayday, Madeline Y.
Khan, Lillian M.
Chow, Eric D.
Zinter, Matt S.
DeRisi, Joseph L.
Miniaturization and optimization of 384-well compatible RNA sequencing library preparation
title Miniaturization and optimization of 384-well compatible RNA sequencing library preparation
title_full Miniaturization and optimization of 384-well compatible RNA sequencing library preparation
title_fullStr Miniaturization and optimization of 384-well compatible RNA sequencing library preparation
title_full_unstemmed Miniaturization and optimization of 384-well compatible RNA sequencing library preparation
title_short Miniaturization and optimization of 384-well compatible RNA sequencing library preparation
title_sort miniaturization and optimization of 384-well compatible rna sequencing library preparation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328170/
https://www.ncbi.nlm.nih.gov/pubmed/30629604
http://dx.doi.org/10.1371/journal.pone.0206194
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