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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
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965376/ https://www.ncbi.nlm.nih.gov/pubmed/20815917 http://dx.doi.org/10.1186/gb-2010-11-9-132 |