Using False Discovery Rates to Benchmark SNP-callers in next-generation sequencing projects

Sequence alignments form the basis for many comparative and population genomic studies. Alignment tools provide a range of accuracies dependent on the divergence between the sequences and the alignment methods. Despite widespread use, there is no standard method for assessing the accuracy of a datas...

Descripción completa

Detalles Bibliográficos
Autores principales: Farrer, Rhys A., Henk, Daniel A., MacLean, Dan, Studholme, David J., Fisher, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3604800/
https://www.ncbi.nlm.nih.gov/pubmed/23518929
http://dx.doi.org/10.1038/srep01512

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3604800/
https://www.ncbi.nlm.nih.gov/pubmed/23518929
http://dx.doi.org/10.1038/srep01512

Ejemplares similares