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...

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Detalles Bibliográficos
Autores principales: Söylev, Arda, Çokoglu, Sevim Seda, Koptekin, Dilek, Alkan, Can, Somel, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
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

Internet

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

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