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Exact association test for small size sequencing data
BACKGROUND: Recent statistical methods for next generation sequencing (NGS) data have been successfully applied to identifying rare genetic variants associated with certain diseases. However, most commonly used methods (e.g., burden tests and variance-component tests) rely on large sample sizes. Not...
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| Publicado no: | BMC Med Genomics |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5918458/ https://ncbi.nlm.nih.gov/pubmed/29697368 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-018-0344-z |
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