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A beginner’s guide to assembling a draft genome and analyzing structural variants with long-read sequencing technologies
Advances in long-read DNA sequencing technologies have enabled researchers to obtain high-quality genomes and finely resolve structural variants (SVs) in many species, even from small laboratories. The hands-on protocol presented here will guide you through the process of analyzing three different t...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9254108/ https://www.ncbi.nlm.nih.gov/pubmed/35776635 http://dx.doi.org/10.1016/j.xpro.2022.101506 |