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Insertion variants missing in the human reference genome are widespread among human populations
BACKGROUND: Structural variants comprise diverse genomic arrangements including deletions, insertions, inversions, and translocations, which can generally be detected in humans through sequence comparison to the reference genome. Among structural variants, insertions are the least frequently identif...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666470/ https://www.ncbi.nlm.nih.gov/pubmed/33187521 http://dx.doi.org/10.1186/s12915-020-00894-1 |