Resolving the complexity of the human genome using single-molecule sequencing

The human genome is arguably the most complete mammalian reference assembly(1–3) yet more than 160 euchromatic gaps remain(4–6) and aspects of its structural variation remain poorly understood ten years after its completion(7–9). In order to identify missing sequence and genetic variation, we sequen...

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Detalhes bibliográficos
Publicado no:Nature
Main Authors: Chaisson, Mark J.P., Huddleston, John, Dennis, Megan Y., Sudmant, Peter H., Malig, Maika, Hormozdiari, Fereydoun, Antonacci, Francesca, Surti, Urvashi, Sandstrom, Richard, Boitano, Matthew, Landolin, Jane M., Stamatoyannopoulos, John A., Hunkapiller, Michael W., Korlach, Jonas, Eichler, Evan E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4317254/
https://ncbi.nlm.nih.gov/pubmed/25383537
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature13907
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