000 01199 a2200325 4500
005 20250517131648.0
264 0 _c20180814
008 201808s 0 0 eng d
022 _a1468-6244
024 7 _a10.1136/jmedgenet-2016-104369
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLiu, Xiaoming
245 0 0 _aThe performance of deleteriousness prediction scores for rare non-protein-changing single nucleotide variants in human genes.
_h[electronic resource]
260 _bJournal of medical genetics
_c02 2017
300 _a134-144 p.
_bdigital
500 _aPublication Type: Letter; Research Support, N.I.H., Extramural
650 0 4 _aDatabases, Genetic
650 0 4 _aGenes
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenome, Human
650 0 4 _aGenome-Wide Association Study
_xmethods
650 0 4 _aHumans
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aROC Curve
650 0 4 _aReproducibility of Results
700 1 _aLi, Chang
700 1 _aBoerwinkle, Eric
773 0 _tJournal of medical genetics
_gvol. 54
_gno. 2
_gp. 134-144
856 4 0 _uhttps://doi.org/10.1136/jmedgenet-2016-104369
_zAvailable from publisher's website
999 _c26717461
_d26717461