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SMaSH: a benchmarking toolkit for human genome variant calling
Motivation: Computational methods are essential to extract actionable information from raw sequencing data, and to thus fulfill the promise of next-generation sequencing technology. Unfortunately, computational tools developed to call variants from human sequencing data disagree on many of their pre...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4173010/ https://ncbi.nlm.nih.gov/pubmed/24894505 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu345 |
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