000 01232 a2200349 4500
005 20250517010941.0
264 0 _c20150806
008 201508s 0 0 eng d
022 _a1098-2272
024 7 _a10.1002/gepi.21873
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPeil, Barbara
245 0 0 _aTailored selection of study individuals to be sequenced in order to improve the accuracy of genotype imputation.
_h[electronic resource]
260 _bGenetic epidemiology
_cFeb 2015
300 _a114-21 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChromosomes, Human, Pair 22
_xgenetics
650 0 4 _aGenetic Variation
650 0 4 _aGenotype
650 0 4 _aHapMap Project
650 0 4 _aHumans
650 0 4 _aMajor Histocompatibility Complex
_xgenetics
650 0 4 _aPrincipal Component Analysis
650 0 4 _aRacial Groups
_xgenetics
650 0 4 _aSoftware
700 1 _aKabisch, Maria
700 1 _aFischer, Christine
700 1 _aHamann, Ute
700 1 _aBermejo, Justo Lorenzo
773 0 _tGenetic epidemiology
_gvol. 39
_gno. 2
_gp. 114-21
856 4 0 _uhttps://doi.org/10.1002/gepi.21873
_zAvailable from publisher's website
999 _c24485602
_d24485602