A new method to measure the semantic similarity from query phenotypic abnormalities to diseases based on the human phenotype ontology
Abstract Background Although rapid developed sequencing technologies make it possible for genotype data to be used in clinical diagnosis, it is still challenging for clinicians to understand the results of sequencing and make correct judgement based on them. Before this, diagnosis based on clinical...
Guardat en:
| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2018-05-01
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| Col·lecció: | BMC Bioinformatics |
| Matèries: | |
| Accés en línia: | http://link.springer.com/article/10.1186/s12859-018-2064-y |
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