| 000 | 01186 a2200337 4500 | ||
|---|---|---|---|
| 005 | 20250516073027.0 | ||
| 264 | 0 | _c20120810 | |
| 008 | 201208s 0 0 eng d | ||
| 022 | _a1367-4811 | ||
| 024 | 7 |
_a10.1093/bioinformatics/bts019 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aEmde, Anne-Katrin | |
| 245 | 0 | 0 |
_aDetecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. _h[electronic resource] |
| 260 |
_bBioinformatics (Oxford, England) _cMar 2012 |
||
| 300 |
_a619-27 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAlgorithms |
| 650 | 0 | 4 |
_aGenomics _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aINDEL Mutation |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 700 | 1 | _aSchulz, Marcel H | |
| 700 | 1 | _aWeese, David | |
| 700 | 1 | _aSun, Ruping | |
| 700 | 1 | _aVingron, Martin | |
| 700 | 1 | _aKalscheuer, Vera M | |
| 700 | 1 | _aHaas, Stefan A | |
| 700 | 1 | _aReinert, Knut | |
| 773 | 0 |
_tBioinformatics (Oxford, England) _gvol. 28 _gno. 5 _gp. 619-27 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/bioinformatics/bts019 _zAvailable from publisher's website |
| 999 |
_c21454769 _d21454769 |
||