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Bead-linked transposomes enable a normalization-free workflow for NGS library preparation

BACKGROUND: Transposome-based technologies have enabled the streamlined production of sequencer-ready DNA libraries; however, current methods are highly sensitive to the amount and quality of input nucleic acid. RESULTS: We describe a new library preparation technology (Nextera DNA Flex) that utiliz...

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Autores principales: Bruinsma, Stephen, Burgess, Joshua, Schlingman, Daniel, Czyz, Agata, Morrell, Natalie, Ballenger, Catherine, Meinholz, Heather, Brady, Lee, Khanna, Anupama, Freeberg, Lindsay, Jackson, Rosamond G, Mathonet, Pascale, Verity, Susan C, Slatter, Andrew F, Golshani, Rooz, Grunenwald, Haiying, Schroth, Gary P, Gormley, Niall A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167868/
https://www.ncbi.nlm.nih.gov/pubmed/30285621
http://dx.doi.org/10.1186/s12864-018-5096-9
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author Bruinsma, Stephen
Burgess, Joshua
Schlingman, Daniel
Czyz, Agata
Morrell, Natalie
Ballenger, Catherine
Meinholz, Heather
Brady, Lee
Khanna, Anupama
Freeberg, Lindsay
Jackson, Rosamond G
Mathonet, Pascale
Verity, Susan C
Slatter, Andrew F
Golshani, Rooz
Grunenwald, Haiying
Schroth, Gary P
Gormley, Niall A
author_facet Bruinsma, Stephen
Burgess, Joshua
Schlingman, Daniel
Czyz, Agata
Morrell, Natalie
Ballenger, Catherine
Meinholz, Heather
Brady, Lee
Khanna, Anupama
Freeberg, Lindsay
Jackson, Rosamond G
Mathonet, Pascale
Verity, Susan C
Slatter, Andrew F
Golshani, Rooz
Grunenwald, Haiying
Schroth, Gary P
Gormley, Niall A
author_sort Bruinsma, Stephen
collection PubMed
description BACKGROUND: Transposome-based technologies have enabled the streamlined production of sequencer-ready DNA libraries; however, current methods are highly sensitive to the amount and quality of input nucleic acid. RESULTS: We describe a new library preparation technology (Nextera DNA Flex) that utilizes a known concentration of transposomes conjugated directly to beads to bind a fixed amount of DNA, and enables direct input of blood and saliva using an integrated extraction protocol. We further report results from libraries generated outside the standard parameters of the workflow, highlighting novel applications for Nextera DNA Flex, including human genome builds and variant calling from below 1 ng DNA input, customization of insert size, and preparation of libraries from short fragments and severely degraded FFPE samples. Using this bead-linked library preparation method, library yield saturation was observed at an input amount of 100 ng. Preparation of libraries from a range of species with varying GC levels demonstrated uniform coverage of small genomes. For large and complex genomes, coverage across the genome, including difficult regions, was improved compared with other library preparation methods. Libraries were successfully generated from amplicons of varying sizes (from 50 bp to 11 kb), however, a decrease in efficiency was observed for amplicons smaller than 250 bp. This library preparation method was also compatible with poor-quality DNA samples, with sequenceable libraries prepared from formalin-fixed paraffin-embedded samples with varying levels of degradation. CONCLUSIONS: In contrast to solution-based library preparation, this bead-based technology produces a normalized, sequencing-ready library for a wide range of DNA input types and amounts, largely obviating the need for DNA quantitation. The robustness of this bead-based library preparation kit and flexibility of input DNA facilitates application across a wide range of fields.
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spelling pubmed-61678682018-10-09 Bead-linked transposomes enable a normalization-free workflow for NGS library preparation Bruinsma, Stephen Burgess, Joshua Schlingman, Daniel Czyz, Agata Morrell, Natalie Ballenger, Catherine Meinholz, Heather Brady, Lee Khanna, Anupama Freeberg, Lindsay Jackson, Rosamond G Mathonet, Pascale Verity, Susan C Slatter, Andrew F Golshani, Rooz Grunenwald, Haiying Schroth, Gary P Gormley, Niall A BMC Genomics Research Article BACKGROUND: Transposome-based technologies have enabled the streamlined production of sequencer-ready DNA libraries; however, current methods are highly sensitive to the amount and quality of input nucleic acid. RESULTS: We describe a new library preparation technology (Nextera DNA Flex) that utilizes a known concentration of transposomes conjugated directly to beads to bind a fixed amount of DNA, and enables direct input of blood and saliva using an integrated extraction protocol. We further report results from libraries generated outside the standard parameters of the workflow, highlighting novel applications for Nextera DNA Flex, including human genome builds and variant calling from below 1 ng DNA input, customization of insert size, and preparation of libraries from short fragments and severely degraded FFPE samples. Using this bead-linked library preparation method, library yield saturation was observed at an input amount of 100 ng. Preparation of libraries from a range of species with varying GC levels demonstrated uniform coverage of small genomes. For large and complex genomes, coverage across the genome, including difficult regions, was improved compared with other library preparation methods. Libraries were successfully generated from amplicons of varying sizes (from 50 bp to 11 kb), however, a decrease in efficiency was observed for amplicons smaller than 250 bp. This library preparation method was also compatible with poor-quality DNA samples, with sequenceable libraries prepared from formalin-fixed paraffin-embedded samples with varying levels of degradation. CONCLUSIONS: In contrast to solution-based library preparation, this bead-based technology produces a normalized, sequencing-ready library for a wide range of DNA input types and amounts, largely obviating the need for DNA quantitation. The robustness of this bead-based library preparation kit and flexibility of input DNA facilitates application across a wide range of fields. BioMed Central 2018-10-01 /pmc/articles/PMC6167868/ /pubmed/30285621 http://dx.doi.org/10.1186/s12864-018-5096-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bruinsma, Stephen
Burgess, Joshua
Schlingman, Daniel
Czyz, Agata
Morrell, Natalie
Ballenger, Catherine
Meinholz, Heather
Brady, Lee
Khanna, Anupama
Freeberg, Lindsay
Jackson, Rosamond G
Mathonet, Pascale
Verity, Susan C
Slatter, Andrew F
Golshani, Rooz
Grunenwald, Haiying
Schroth, Gary P
Gormley, Niall A
Bead-linked transposomes enable a normalization-free workflow for NGS library preparation
title Bead-linked transposomes enable a normalization-free workflow for NGS library preparation
title_full Bead-linked transposomes enable a normalization-free workflow for NGS library preparation
title_fullStr Bead-linked transposomes enable a normalization-free workflow for NGS library preparation
title_full_unstemmed Bead-linked transposomes enable a normalization-free workflow for NGS library preparation
title_short Bead-linked transposomes enable a normalization-free workflow for NGS library preparation
title_sort bead-linked transposomes enable a normalization-free workflow for ngs library preparation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167868/
https://www.ncbi.nlm.nih.gov/pubmed/30285621
http://dx.doi.org/10.1186/s12864-018-5096-9
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