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Atlas of Cryptic Genetic Relatedness Among 1000 Human Genomes
A novel computational method for detecting identical-by-descent (IBD) chromosomal segments between sequenced genomes is presented. It utilizes the distribution patterns of very rare genetic variants (vrGVs), which have minor allele frequencies <0.2%. Contrary to the existing probabilistic approac...
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| Publicat a: | Genome Biol Evol |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4824066/ https://ncbi.nlm.nih.gov/pubmed/26907499 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/gbe/evw034 |
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