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De novo diploid genome assembly for genome-wide structural variant detection

Detection of structural variants (SVs) on the basis of read alignment to a reference genome remains a difficult problem. De novo assembly, traditionally used to generate reference genomes, offers an alternative for SV detection. However, it has not been applied broadly to human genomes because of fu...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:NAR Genom Bioinform
Prif Awduron: Zhang, Lu, Zhou, Xin, Weng, Ziming, Sidow, Arend
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2019
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7671403/
https://ncbi.nlm.nih.gov/pubmed/33575568
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nargab/lqz018
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