Clinical phenotype-based gene prioritization: an initial study using semantic similarity and the human phenotype ontology
Exome sequencing is a promising method for diagnosing patients with a complex phenotype. However, variant interpretation relative to patient phenotype can be challenging in some scenarios, particularly clinical assessment of rare complex phenotypes. Each patient's sequence reveals many possibly...
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Veröffentlicht in: | BMC bioinformatics 2014-07, Vol.15 (1), p.248-248, Article 248 |
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Sprache: | eng |
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