000 01440 a2200397 4500
005 20250517045603.0
264 0 _c20160614
008 201606s 0 0 eng d
022 _a1367-4811
024 7 _a10.1093/bioinformatics/btv473
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aAntanaviciute, Agne
245 0 0 _aOVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization.
_h[electronic resource]
260 _bBioinformatics (Oxford, England)
_cDec 2015
300 _a3822-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlgorithms
650 0 4 _aBiological Ontologies
650 0 4 _aComputational Biology
_xmethods
650 0 4 _aDisease
_xgenetics
650 0 4 _aExome
_xgenetics
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aPhenotype
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
650 0 4 _aTranscriptome
700 1 _aWatson, Christopher M
700 1 _aHarrison, Sally M
700 1 _aLascelles, Carolina
700 1 _aCrinnion, Laura
700 1 _aMarkham, Alexander F
700 1 _aBonthron, David T
700 1 _aCarr, Ian M
773 0 _tBioinformatics (Oxford, England)
_gvol. 31
_gno. 23
_gp. 3822-9
856 4 0 _uhttps://doi.org/10.1093/bioinformatics/btv473
_zAvailable from publisher's website
999 _c25168842
_d25168842