| 000 | 01294 a2200385 4500 | ||
|---|---|---|---|
| 005 | 20250517155340.0 | ||
| 264 | 0 | _c20181214 | |
| 008 | 201812s 0 0 eng d | ||
| 022 | _a2045-2322 | ||
| 024 | 7 |
_a10.1038/s41598-017-02487-5 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPajuste, Fanny-Dhelia | |
| 245 | 0 | 0 |
_aFastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads. _h[electronic resource] |
| 260 |
_bScientific reports _c05 2017 |
||
| 300 |
_a2537 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAlgorithms |
| 650 | 0 | 4 | _aBayes Theorem |
| 650 | 0 | 4 | _aBenchmarking |
| 650 | 0 | 4 | _aGenome, Human |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHigh-Throughput Nucleotide Sequencing |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aReproducibility of Results |
| 650 | 0 | 4 |
_aSequence Analysis, DNA _xmethods |
| 650 | 0 | 4 | _aSoftware |
| 700 | 1 | _aKaplinski, Lauris | |
| 700 | 1 | _aMöls, Märt | |
| 700 | 1 | _aPuurand, Tarmo | |
| 700 | 1 | _aLepamets, Maarja | |
| 700 | 1 | _aRemm, Maido | |
| 773 | 0 |
_tScientific reports _gvol. 7 _gno. 1 _gp. 2537 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/s41598-017-02487-5 _zAvailable from publisher's website |
| 999 |
_c27231626 _d27231626 |
||