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PGG.SV: a whole-genome-sequencing-based structural variant resource and data analysis platform
Structural variations (SVs) play important roles in human evolution and diseases, but there is a lack of data resources concerning representative samples, especially for East Asians. Taking advantage of both next-generation sequencing and third-generation sequencing data at the whole-genome level, w...
| Autores principales: | , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825616/ https://www.ncbi.nlm.nih.gov/pubmed/36243989 http://dx.doi.org/10.1093/nar/gkac905 |