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
Hauptverfasser: Masino, Aaron J, Dechene, Elizabeth T, Dulik, Matthew C, Wilkens, Alisha, Spinner, Nancy B, Krantz, Ian D, Pennington, Jeffrey W, Robinson, Peter N, White, Peter S
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Sprache:eng
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