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CONGA: Copy number variation genotyping in ancient genomes and low-coverage sequencing data
To date, ancient genome analyses have been largely confined to the study of single nucleotide polymorphisms (SNPs). Copy number variants (CNVs) are a major contributor of disease and of evolutionary adaptation, but identifying CNVs in ancient shotgun-sequenced genomes is hampered by typical low geno...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9873172/ https://www.ncbi.nlm.nih.gov/pubmed/36516232 http://dx.doi.org/10.1371/journal.pcbi.1010788 |