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Whole-genome resequencing allows detection of many rare LINE-1 insertion alleles in humans
High-throughput sequencing has recently begun to revolutionize the study of structural variants in the genomes of humans and other species. More recently, this technology and others have been applied to the study of human retrotransposon insertion polymorphisms (RIPs), yielding an unprecedented cata...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Cold Spring Harbor Laboratory Press
2011
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3106331/ https://ncbi.nlm.nih.gov/pubmed/20980553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.114777.110 |
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