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A study on fast calling variants from next-generation sequencing data using decision tree
BACKGROUND: The rapid development of next-generation sequencing (NGS) technology has continuously been refreshing the throughput of sequencing data. However, due to the lack of a smart tool that is both fast and accurate, the analysis task for NGS data, especially those with low-coverage, remains ch...
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| Publicado no: | BMC Bioinformatics |
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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/PMC5907718/ https://ncbi.nlm.nih.gov/pubmed/29673316 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2147-9 |
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