Xdrop: Targeted sequencing of long DNA molecules from low input samples using droplet sorting

Long‐read sequencing can resolve regions of the genome that are inaccessible to short reads, and therefore are ideal for genome‐gap closure, solving structural rearrangements and sequencing through repetitive elements. Here we introduce the Xdrop technology: a novel microfluidic‐based system that al...

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Detalles Bibliográficos
Autores principales: Madsen, Esben B., Höijer, Ida, Kvist, Thomas, Ameur, Adam, Mikkelsen, Marie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Methods
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496172/
https://www.ncbi.nlm.nih.gov/pubmed/32516842
http://dx.doi.org/10.1002/humu.24063

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496172/
https://www.ncbi.nlm.nih.gov/pubmed/32516842
http://dx.doi.org/10.1002/humu.24063

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