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Critical length in long-read resequencing

Long-read sequencing has substantial advantages for structural variant discovery and phasing of variants compared to short-read technologies, but the required and optimal read length has not been assessed. In this work, we used long reads simulated from human genomes and evaluated structural variant...

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Bibliografische gegevens
Gepubliceerd in:NAR Genom Bioinform
Hoofdauteurs: De Coster, Wouter, Strazisar, Mojca, De Rijk, Peter
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2020
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7671308/
https://ncbi.nlm.nih.gov/pubmed/33575574
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nargab/lqz027
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