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The first Irish genome and ways of improving sequence accuracy
Whole-genome sequencing of an Irish person reveals hundreds of thousands of novel genomic variants. Imputation using previous known information improves the accuracy of low-read-depth sequencing. See research article: http://genomebiology.com/2010/11/9/R91
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2965376/ https://ncbi.nlm.nih.gov/pubmed/20815917 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2010-11-9-132 |
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