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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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| Pubblicato in: | NAR Genom Bioinform |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2019
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| Soggetti: | |
| Accesso online: | 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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