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

Detalles Bibliográficos
Autores principales: Ju, Young Seok, Yoo, Yun Joo, Kim, Jong-Il, Seo, Jeong-Sun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Highlight
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
Descripción
Sumario: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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