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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...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3604800/ https://ncbi.nlm.nih.gov/pubmed/23518929 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep01512 |
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