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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | NAR Genom Bioinform |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Oxford University Press
2019
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| 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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