000 01140 a2200313 4500
005 20250518022523.0
264 0 _c20200922
008 202009s 0 0 eng d
022 _a2045-2322
024 7 _a10.1038/s41598-018-38189-9
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSun, Hong
245 0 0 _aNew insights into the pathogenicity of non-synonymous variants through multi-level analysis.
_h[electronic resource]
260 _bScientific reports
_c02 2019
300 _a1667 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aComputational Biology
_xmethods
650 0 4 _aDisease
_xgenetics
650 0 4 _aGenetic Markers
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenome, Human
650 0 4 _aHigh-Throughput Nucleotide Sequencing
650 0 4 _aHumans
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aSequence Analysis, DNA
_xmethods
700 1 _aYu, Guangjun
773 0 _tScientific reports
_gvol. 9
_gno. 1
_gp. 1667
856 4 0 _uhttps://doi.org/10.1038/s41598-018-38189-9
_zAvailable from publisher's website
999 _c29342480
_d29342480