000 01417 a2200421 4500
005 20250516153302.0
264 0 _c20131231
008 201312s 0 0 eng d
022 _a1367-4811
024 7 _a10.1093/bioinformatics/btt314
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aRaczy, Come
245 0 0 _aIsaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms.
_h[electronic resource]
260 _bBioinformatics (Oxford, England)
_cAug 2013
300 _a2041-3 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aGenetic Variation
650 0 4 _aGenome, Human
650 0 4 _aHigh-Throughput Nucleotide Sequencing
_xmethods
650 0 4 _aHumans
650 0 4 _aSequence Alignment
_xmethods
650 0 4 _aSequence Analysis, DNA
_xmethods
650 0 4 _aSoftware
700 1 _aPetrovski, Roman
700 1 _aSaunders, Christopher T
700 1 _aChorny, Ilya
700 1 _aKruglyak, Semyon
700 1 _aMargulies, Elliott H
700 1 _aChuang, Han-Yu
700 1 _aKällberg, Morten
700 1 _aKumar, Swathi A
700 1 _aLiao, Arnold
700 1 _aLittle, Kristina M
700 1 _aStrömberg, Michael P
700 1 _aTanner, Stephen W
773 0 _tBioinformatics (Oxford, England)
_gvol. 29
_gno. 16
_gp. 2041-3
856 4 0 _uhttps://doi.org/10.1093/bioinformatics/btt314
_zAvailable from publisher's website
999 _c22808072
_d22808072