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Closing Human Reference Genome Gaps: Identifying and Characterizing Gap-Closing Sequences
Despite continuous updates of the human reference genome, there are still hundreds of unresolved gaps which account for about 5% of the total sequence length. Given the availability of whole genome de novo assemblies, especially those derived from long-read sequencing data, gap-closing sequences can...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Genetics Society of America
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7407462/ https://www.ncbi.nlm.nih.gov/pubmed/32532800 http://dx.doi.org/10.1534/g3.120.401280 |