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Nebula: ultra-efficient mapping-free structural variant genotyper
Large scale catalogs of common genetic variants (including indels and structural variants) are being created using data from second and third generation whole-genome sequencing technologies. However, the genotyping of these variants in newly sequenced samples is a nontrivial task that requires exten...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Oxford University Press
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8096284/ https://www.ncbi.nlm.nih.gov/pubmed/33503255 http://dx.doi.org/10.1093/nar/gkab025 |