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Performance assessment of variant calling pipelines using human whole exome sequencing and simulated data
BACKGROUND: Whole exome sequencing (WES) is a cost-effective method that identifies clinical variants but it demands accurate variant caller tools. Currently available tools have variable accuracy in predicting specific clinical variants. But it may be possible to find the best combination of aligne...
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| Publicado en: | BMC Bioinformatics |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6580603/ https://ncbi.nlm.nih.gov/pubmed/31208315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-019-2928-9 |
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