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Set-theory based benchmarking of three different variant callers for targeted sequencing
BACKGROUND: Next generation sequencing (NGS) technologies have improved the study of hereditary diseases. Since the evaluation of bioinformatics pipelines is not straightforward, NGS demands effective strategies to analyze data that is of paramount relevance for decision making under a clinical scen...
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| Publicado no: | BMC Bioinformatics |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7791862/ https://ncbi.nlm.nih.gov/pubmed/33413082 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-03926-3 |
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