000 01333 a2200385 4500
005 20250517215221.0
264 0 _c20190808
008 201908s 0 0 eng d
022 _a1362-4962
024 7 _a10.1093/nar/gky407
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHuang, Dandan
245 0 0 _aGWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.
_h[electronic resource]
260 _bNucleic acids research
_c07 2018
300 _aW114-W120 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aComputational Biology
_xtrends
650 0 4 _aGenetic Diseases, Inborn
650 0 4 _aGenome-Wide Association Study
650 0 4 _aGenomics
_xmethods
650 0 4 _aHumans
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
650 0 4 _aQuantitative Trait Loci
_xgenetics
650 0 4 _aSoftware
700 1 _aYi, Xianfu
700 1 _aZhang, Shijie
700 1 _aZheng, Zhanye
700 1 _aWang, Panwen
700 1 _aXuan, Chenghao
700 1 _aSham, Pak Chung
700 1 _aWang, Junwen
700 1 _aLi, Mulin Jun
773 0 _tNucleic acids research
_gvol. 46
_gno. W1
_gp. W114-W120
856 4 0 _uhttps://doi.org/10.1093/nar/gky407
_zAvailable from publisher's website
999 _c28401097
_d28401097