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A new method to measure the semantic similarity from query phenotypic abnormalities to diseases based on the human phenotype ontology

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 features...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Bioinformatics
Egile Nagusiak: Gong, Xiaofeng, Jiang, Jianping, Duan, Zhongqu, Lu, Hui
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2018
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5998886/
https://ncbi.nlm.nih.gov/pubmed/29745853
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2064-y
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