A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome

Methods to reconstruct the mitochondrial DNA (mtDNA) sequence using short-read sequencing come with an inherent bias due to amplification and mapping. They can fail to determine the phase of variants, to capture multiple deletions and to cover the mitochondrial genome evenly. Here we describe a meth...

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Detalles Bibliográficos
Autores principales: Keraite, Ieva, Becker, Philipp, Canevazzi, Davide, Frias-López, Cristina, Dabad, Marc, Tonda-Hernandez, Raúl, Paramonov, Ida, Ingham, Matthew John, Brun-Heath, Isabelle, Leno, Jordi, Abulí, Anna, Garcia-Arumí, Elena, Heath, Simon Charles, Gut, Marta, Gut, Ivo Glynne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537161/
https://www.ncbi.nlm.nih.gov/pubmed/36202811
http://dx.doi.org/10.1038/s41467-022-33530-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537161/
https://www.ncbi.nlm.nih.gov/pubmed/36202811
http://dx.doi.org/10.1038/s41467-022-33530-3

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