000 01293 a2200361 4500
005 20250516103246.0
264 0 _c20130605
008 201306s 0 0 eng d
022 _a1367-4811
024 7 _a10.1093/bioinformatics/bts462
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKamphans, Tom
245 0 0 _aGeneTalk: an expert exchange platform for assessing rare sequence variants in personal genomes.
_h[electronic resource]
260 _bBioinformatics (Oxford, England)
_cOct 2012
300 _a2515-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aComputational Biology
_xmethods
650 0 4 _aExome
650 0 4 _aGenome, Human
650 0 4 _aHumans
650 0 4 _aInformation Dissemination
_xmethods
650 0 4 _aInternet
650 0 4 _aKnowledge Management
650 0 4 _aMolecular Sequence Annotation
650 0 4 _aPolymorphism, Genetic
650 0 4 _aPrecision Medicine
650 0 4 _aSequence Analysis, DNA
_xmethods
650 0 4 _aSoftware
650 0 4 _aUser-Computer Interface
700 1 _aKrawitz, Peter M
773 0 _tBioinformatics (Oxford, England)
_gvol. 28
_gno. 19
_gp. 2515-6
856 4 0 _uhttps://doi.org/10.1093/bioinformatics/bts462
_zAvailable from publisher's website
999 _c21969975
_d21969975