| 000 | 01313 a2200361 4500 | ||
|---|---|---|---|
| 005 | 20250517054935.0 | ||
| 264 | 0 | _c20160915 | |
| 008 | 201609s 0 0 eng d | ||
| 022 | _a1934-8258 | ||
| 024 | 7 |
_a10.1002/0471142905.hg0725s87 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWare, James S | |
| 245 | 0 | 0 |
_aInterpreting de novo Variation in Human Disease Using denovolyzeR. _h[electronic resource] |
| 260 |
_bCurrent protocols in human genetics _cOct 2015 |
||
| 300 |
_a7.25.1-7.25.15 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aComputational Biology _xmethods |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 |
_aGenome-Wide Association Study _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aModels, Genetic |
| 650 | 0 | 4 | _aModels, Statistical |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aSoftware |
| 700 | 1 | _aSamocha, Kaitlin E | |
| 700 | 1 | _aHomsy, Jason | |
| 700 | 1 | _aDaly, Mark J | |
| 773 | 0 |
_tCurrent protocols in human genetics _gvol. 87 _gp. 7.25.1-7.25.15 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/0471142905.hg0725s87 _zAvailable from publisher's website |
| 999 |
_c25327774 _d25327774 |
||