A novel and well-defined benchmarking method for second generation read mapping

BACKGROUND: Second generation sequencing technologies yield DNA sequence data at ultra high-throughput. Common to most biological applications is a mapping of the reads to an almost identical or highly similar reference genome. The assessment of the quality of read mapping results is not straightfor...

Descripción completa

Detalles Bibliográficos
Autores principales: Holtgrewe, Manuel, Emde, Anne-Katrin, Weese, David, Reinert, Knut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128034/
https://www.ncbi.nlm.nih.gov/pubmed/21615913
http://dx.doi.org/10.1186/1471-2105-12-210

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128034/
https://www.ncbi.nlm.nih.gov/pubmed/21615913
http://dx.doi.org/10.1186/1471-2105-12-210

Ejemplares similares