| 000 | 01433 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250517093038.0 | ||
| 264 | 0 | _c20170327 | |
| 008 | 201703s 0 0 eng d | ||
| 022 | _a1932-6203 | ||
| 024 | 7 |
_a10.1371/journal.pone.0154181 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aRichardson, Tom G | |
| 245 | 0 | 0 |
_aIncorporating Non-Coding Annotations into Rare Variant Analysis. _h[electronic resource] |
| 260 |
_bPloS one _c2016 |
||
| 300 |
_ae0154181 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 |
_aComputational Biology _xmethods |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xdiagnosis |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 |
_aGenome, Human _xgenetics |
| 650 | 0 | 4 |
_aGenome-Wide Association Study _xmethods |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aHigh-Throughput Nucleotide Sequencing _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMolecular Sequence Annotation _xmethods |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aUnited Kingdom |
| 700 | 1 | _aCampbell, Colin | |
| 700 | 1 | _aTimpson, Nicholas J | |
| 700 | 1 | _aGaunt, Tom R | |
| 773 | 0 |
_tPloS one _gvol. 11 _gno. 4 _gp. e0154181 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1371/journal.pone.0154181 _zAvailable from publisher's website |
| 999 |
_c25971772 _d25971772 |
||