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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group
2013
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| Materias: | |
| 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 |