000 01406 a2200433 4500
005 20250517010007.0
264 0 _c20150924
008 201509s 0 0 eng d
022 _a1423-0062
024 7 _a10.1159/000368676
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDrichel, Dmitriy
245 0 0 _aRare variant testing of imputed data: an analysis pipeline typified.
_h[electronic resource]
260 _bHuman heredity
_c2014
300 _a164-78 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAlzheimer Disease
_xepidemiology
650 0 4 _aCase-Control Studies
650 0 4 _aGenetic Variation
650 0 4 _aGenome, Human
650 0 4 _aGenome-Wide Association Study
_xstatistics & numerical data
650 0 4 _aGenotype
650 0 4 _aGermany
_xepidemiology
650 0 4 _aHumans
650 0 4 _aModels, Statistical
650 0 4 _aRegression Analysis
650 0 4 _aSoftware
700 1 _aHerold, Christine
700 1 _aLacour, André
700 1 _aRamirez, Alfredo
700 1 _aJessen, Frank
700 1 _aMaier, Wolfgang
700 1 _aNoethen, Markus M
700 1 _aLeber, Markus
700 1 _aVaitsiakhovich, Tatsiana
700 1 _aBecker, Tim
773 0 _tHuman heredity
_gvol. 78
_gno. 3-4
_gp. 164-78
856 4 0 _uhttps://doi.org/10.1159/000368676
_zAvailable from publisher's website
999 _c24456313
_d24456313