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Selective single molecule sequencing and assembly of a human Y chromosome of African origin

Mammalian Y chromosomes are often neglected from genomic analysis. Due to their inherent assembly difficulties, high repeat content, and large ampliconic regions, only a handful of species have their Y chromosome properly characterized. To date, just a single human reference quality Y chromosome, of...

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Autores principales: Kuderna, Lukas F. K., Lizano, Esther, Julià, Eva, Gomez-Garrido, Jessica, Serres-Armero, Aitor, Kuhlwilm, Martin, Alandes, Regina Antoni, Alvarez-Estape, Marina, Juan, David, Simon, Heath, Alioto, Tyler, Gut, Marta, Gut, Ivo, Schierup, Mikkel Heide, Fornas, Oscar, Marques-Bonet, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315018/
https://www.ncbi.nlm.nih.gov/pubmed/30602775
http://dx.doi.org/10.1038/s41467-018-07885-5
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author Kuderna, Lukas F. K.
Lizano, Esther
Julià, Eva
Gomez-Garrido, Jessica
Serres-Armero, Aitor
Kuhlwilm, Martin
Alandes, Regina Antoni
Alvarez-Estape, Marina
Juan, David
Simon, Heath
Alioto, Tyler
Gut, Marta
Gut, Ivo
Schierup, Mikkel Heide
Fornas, Oscar
Marques-Bonet, Tomas
author_facet Kuderna, Lukas F. K.
Lizano, Esther
Julià, Eva
Gomez-Garrido, Jessica
Serres-Armero, Aitor
Kuhlwilm, Martin
Alandes, Regina Antoni
Alvarez-Estape, Marina
Juan, David
Simon, Heath
Alioto, Tyler
Gut, Marta
Gut, Ivo
Schierup, Mikkel Heide
Fornas, Oscar
Marques-Bonet, Tomas
author_sort Kuderna, Lukas F. K.
collection PubMed
description Mammalian Y chromosomes are often neglected from genomic analysis. Due to their inherent assembly difficulties, high repeat content, and large ampliconic regions, only a handful of species have their Y chromosome properly characterized. To date, just a single human reference quality Y chromosome, of European ancestry, is available due to a lack of accessible methodology. To facilitate the assembly of such complicated genomic territory, we developed a novel strategy to sequence native, unamplified flow sorted DNA on a MinION nanopore sequencing device. Our approach yields a highly continuous assembly of the first human Y chromosome of African origin. It constitutes a significant improvement over comparable previous methods, increasing continuity by more than 800%. Sequencing native DNA also allows to take advantage of the nanopore signal data to detect epigenetic modifications in situ. This approach is in theory generalizable to any species simplifying the assembly of extremely large and repetitive genomes.
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spelling pubmed-63150182019-01-04 Selective single molecule sequencing and assembly of a human Y chromosome of African origin Kuderna, Lukas F. K. Lizano, Esther Julià, Eva Gomez-Garrido, Jessica Serres-Armero, Aitor Kuhlwilm, Martin Alandes, Regina Antoni Alvarez-Estape, Marina Juan, David Simon, Heath Alioto, Tyler Gut, Marta Gut, Ivo Schierup, Mikkel Heide Fornas, Oscar Marques-Bonet, Tomas Nat Commun Article Mammalian Y chromosomes are often neglected from genomic analysis. Due to their inherent assembly difficulties, high repeat content, and large ampliconic regions, only a handful of species have their Y chromosome properly characterized. To date, just a single human reference quality Y chromosome, of European ancestry, is available due to a lack of accessible methodology. To facilitate the assembly of such complicated genomic territory, we developed a novel strategy to sequence native, unamplified flow sorted DNA on a MinION nanopore sequencing device. Our approach yields a highly continuous assembly of the first human Y chromosome of African origin. It constitutes a significant improvement over comparable previous methods, increasing continuity by more than 800%. Sequencing native DNA also allows to take advantage of the nanopore signal data to detect epigenetic modifications in situ. This approach is in theory generalizable to any species simplifying the assembly of extremely large and repetitive genomes. Nature Publishing Group UK 2019-01-02 /pmc/articles/PMC6315018/ /pubmed/30602775 http://dx.doi.org/10.1038/s41467-018-07885-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kuderna, Lukas F. K.
Lizano, Esther
Julià, Eva
Gomez-Garrido, Jessica
Serres-Armero, Aitor
Kuhlwilm, Martin
Alandes, Regina Antoni
Alvarez-Estape, Marina
Juan, David
Simon, Heath
Alioto, Tyler
Gut, Marta
Gut, Ivo
Schierup, Mikkel Heide
Fornas, Oscar
Marques-Bonet, Tomas
Selective single molecule sequencing and assembly of a human Y chromosome of African origin
title Selective single molecule sequencing and assembly of a human Y chromosome of African origin
title_full Selective single molecule sequencing and assembly of a human Y chromosome of African origin
title_fullStr Selective single molecule sequencing and assembly of a human Y chromosome of African origin
title_full_unstemmed Selective single molecule sequencing and assembly of a human Y chromosome of African origin
title_short Selective single molecule sequencing and assembly of a human Y chromosome of African origin
title_sort selective single molecule sequencing and assembly of a human y chromosome of african origin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315018/
https://www.ncbi.nlm.nih.gov/pubmed/30602775
http://dx.doi.org/10.1038/s41467-018-07885-5
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