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Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets

Despite remarkable progress in DNA sequencing technologies there remains a trade-off between short-read platforms, having limited ability to sequence homopolymers, repeated motifs or long-range structural variation, and long-read platforms, which tend to have lower accuracy and/or throughput. Moreov...

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Autores principales: Puchtler, Tim J, Johnson, Kerr, Palmer, Rebecca N, Talbot, Emma L, Ibbotson, Lindsey A, Powalowska, Paulina K, Knox, Rachel, Shibahara, Aya, M. S. Cunha, Pedro, Newell, Oliver J, Wu, Mei, Chana, Jasmin, Athanasopoulou, Evangelia-Nefeli, Waeber, Andreas M, Stolarek, Magdalena, Silva, Ana-Luisa, Mordaka, Justyna M, Haggis-Powell, Michael, Xyrafaki, Christina, Bush, James, Topkaya, Ibrahim S, Sosna, Maciej, Ingham, Richard J, Huckvale, Thomas, Negrea, Aurel, Breiner, Boris, Šlikas, Justinas, Kelly, Douglas J, Dunning, Alexander J, Bell, Neil M, Dethlefsen, Mark, Love, David M, Dear, Paul H, Kuleshova, Jekaterina, Podd, Gareth J, Isaac, Tom H, Balmforth, Barnaby W, Frayling, Cameron A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736801/
https://www.ncbi.nlm.nih.gov/pubmed/33152076
http://dx.doi.org/10.1093/nar/gkaa987
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author Puchtler, Tim J
Johnson, Kerr
Palmer, Rebecca N
Talbot, Emma L
Ibbotson, Lindsey A
Powalowska, Paulina K
Knox, Rachel
Shibahara, Aya
M. S. Cunha, Pedro
Newell, Oliver J
Wu, Mei
Chana, Jasmin
Athanasopoulou, Evangelia-Nefeli
Waeber, Andreas M
Stolarek, Magdalena
Silva, Ana-Luisa
Mordaka, Justyna M
Haggis-Powell, Michael
Xyrafaki, Christina
Bush, James
Topkaya, Ibrahim S
Sosna, Maciej
Ingham, Richard J
Huckvale, Thomas
Negrea, Aurel
Breiner, Boris
Šlikas, Justinas
Kelly, Douglas J
Dunning, Alexander J
Bell, Neil M
Dethlefsen, Mark
Love, David M
Dear, Paul H
Kuleshova, Jekaterina
Podd, Gareth J
Isaac, Tom H
Balmforth, Barnaby W
Frayling, Cameron A
author_facet Puchtler, Tim J
Johnson, Kerr
Palmer, Rebecca N
Talbot, Emma L
Ibbotson, Lindsey A
Powalowska, Paulina K
Knox, Rachel
Shibahara, Aya
M. S. Cunha, Pedro
Newell, Oliver J
Wu, Mei
Chana, Jasmin
Athanasopoulou, Evangelia-Nefeli
Waeber, Andreas M
Stolarek, Magdalena
Silva, Ana-Luisa
Mordaka, Justyna M
Haggis-Powell, Michael
Xyrafaki, Christina
Bush, James
Topkaya, Ibrahim S
Sosna, Maciej
Ingham, Richard J
Huckvale, Thomas
Negrea, Aurel
Breiner, Boris
Šlikas, Justinas
Kelly, Douglas J
Dunning, Alexander J
Bell, Neil M
Dethlefsen, Mark
Love, David M
Dear, Paul H
Kuleshova, Jekaterina
Podd, Gareth J
Isaac, Tom H
Balmforth, Barnaby W
Frayling, Cameron A
author_sort Puchtler, Tim J
collection PubMed
description Despite remarkable progress in DNA sequencing technologies there remains a trade-off between short-read platforms, having limited ability to sequence homopolymers, repeated motifs or long-range structural variation, and long-read platforms, which tend to have lower accuracy and/or throughput. Moreover, current methods do not allow direct readout of epigenetic modifications from a single read. With the aim of addressing these limitations, we have developed an optical electrowetting sequencing platform that uses step-wise nucleotide triphosphate (dNTP) release, capture and detection in microdroplets from single DNA molecules. Each microdroplet serves as a reaction vessel that identifies an individual dNTP based on a robust fluorescence signal, with the detection chemistry extended to enable detection of 5-methylcytosine. Our platform uses small reagent volumes and inexpensive equipment, paving the way to cost-effective single-molecule DNA sequencing, capable of handling widely varying GC-bias, and demonstrating direct detection of epigenetic modifications.
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spelling pubmed-77368012020-12-17 Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets Puchtler, Tim J Johnson, Kerr Palmer, Rebecca N Talbot, Emma L Ibbotson, Lindsey A Powalowska, Paulina K Knox, Rachel Shibahara, Aya M. S. Cunha, Pedro Newell, Oliver J Wu, Mei Chana, Jasmin Athanasopoulou, Evangelia-Nefeli Waeber, Andreas M Stolarek, Magdalena Silva, Ana-Luisa Mordaka, Justyna M Haggis-Powell, Michael Xyrafaki, Christina Bush, James Topkaya, Ibrahim S Sosna, Maciej Ingham, Richard J Huckvale, Thomas Negrea, Aurel Breiner, Boris Šlikas, Justinas Kelly, Douglas J Dunning, Alexander J Bell, Neil M Dethlefsen, Mark Love, David M Dear, Paul H Kuleshova, Jekaterina Podd, Gareth J Isaac, Tom H Balmforth, Barnaby W Frayling, Cameron A Nucleic Acids Res Methods Online Despite remarkable progress in DNA sequencing technologies there remains a trade-off between short-read platforms, having limited ability to sequence homopolymers, repeated motifs or long-range structural variation, and long-read platforms, which tend to have lower accuracy and/or throughput. Moreover, current methods do not allow direct readout of epigenetic modifications from a single read. With the aim of addressing these limitations, we have developed an optical electrowetting sequencing platform that uses step-wise nucleotide triphosphate (dNTP) release, capture and detection in microdroplets from single DNA molecules. Each microdroplet serves as a reaction vessel that identifies an individual dNTP based on a robust fluorescence signal, with the detection chemistry extended to enable detection of 5-methylcytosine. Our platform uses small reagent volumes and inexpensive equipment, paving the way to cost-effective single-molecule DNA sequencing, capable of handling widely varying GC-bias, and demonstrating direct detection of epigenetic modifications. Oxford University Press 2020-11-05 /pmc/articles/PMC7736801/ /pubmed/33152076 http://dx.doi.org/10.1093/nar/gkaa987 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Puchtler, Tim J
Johnson, Kerr
Palmer, Rebecca N
Talbot, Emma L
Ibbotson, Lindsey A
Powalowska, Paulina K
Knox, Rachel
Shibahara, Aya
M. S. Cunha, Pedro
Newell, Oliver J
Wu, Mei
Chana, Jasmin
Athanasopoulou, Evangelia-Nefeli
Waeber, Andreas M
Stolarek, Magdalena
Silva, Ana-Luisa
Mordaka, Justyna M
Haggis-Powell, Michael
Xyrafaki, Christina
Bush, James
Topkaya, Ibrahim S
Sosna, Maciej
Ingham, Richard J
Huckvale, Thomas
Negrea, Aurel
Breiner, Boris
Šlikas, Justinas
Kelly, Douglas J
Dunning, Alexander J
Bell, Neil M
Dethlefsen, Mark
Love, David M
Dear, Paul H
Kuleshova, Jekaterina
Podd, Gareth J
Isaac, Tom H
Balmforth, Barnaby W
Frayling, Cameron A
Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets
title Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets
title_full Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets
title_fullStr Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets
title_full_unstemmed Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets
title_short Single-molecule DNA sequencing of widely varying GC-content using nucleotide release, capture and detection in microdroplets
title_sort single-molecule dna sequencing of widely varying gc-content using nucleotide release, capture and detection in microdroplets
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736801/
https://www.ncbi.nlm.nih.gov/pubmed/33152076
http://dx.doi.org/10.1093/nar/gkaa987
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