SCOPUS 정보 검색 플랫폼

Nature Methods

Volumn 12, Issue 9, 2015, Pages 841-843

Phenolyzer: Phenotype-based prioritization of candidate genes for human diseases

(3) Yang, Hui a,b Robinson, Peter N c,d,e Wang, Kai a

a UNIVERSITY OF SOUTHERN CALIFORNIA (United States)

b UNIVERSITY OF SOUTHERN CALIFORNIA (United States)

c CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN (Germany)

d MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS (Germany)

e FREIE UNIVERSITÄT BERLIN (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; COMPARATIVE STUDY; COPY NUMBER VARIATION; GENE; GENE FREQUENCY; GENETIC VARIABILITY; GERMLINE MUTATION; HUMAN; HUMAN GENETICS; MACHINE LEARNING; NEXT GENERATION SEQUENCING; PHENOTYPE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; CHROMOSOME MAP; COMPUTER PROGRAM; DATA MINING; DNA SEQUENCE; EXOME; GENETIC DATABASE; GENETIC DISORDER; GENETIC MARKER; GENETIC PREDISPOSITION; GENETICS; HUMAN GENOME; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PROCEDURES;

GENETIC MARKER;

ALGORITHMS; BASE SEQUENCE; CHROMOSOME MAPPING; DATA MINING; DATABASES, GENETIC; EXOME; GENETIC DISEASES, INBORN; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HUMANS; MOLECULAR SEQUENCE DATA; PHENOTYPE; SEQUENCE ANALYSIS, DNA; SOFTWARE;

EID: 84940611109 PISSN: 15487091 EISSN: 15487105 Source Type: Journal
DOI: 10.1038/nmeth.3484 Document Type: Article

Times cited : (292)

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