The evolution and functional impact of human deletion variants shared with archaic hominin genomes

Molecular Biology and Evolution

Volumn 32, Issue 4, 2015, Pages 1008-1019

  Lin, Yen Lung ^a   Pavlidis, Pavlos ^b   Karakoc, Emre ^c   Ajay, Jerry ^d   Gokcumen, Omer ^a  

^a UNIVERSITY AT BUFFALO   (United States)

^b INSTITUTE OF MOLECULAR BIOLOGY AND BIOTECHNOLOGY   (Greece)

^c MAX PLANCK INSTITUTE FOR EVOLUTIONARY BIOLOGY   (Germany)

^d the State University of New York   (United States)

Author keywords

ACOT1; copy number variation (CNV); Denisovan; DMBT1; GHR; GSTT1; LCE3C; Neandertal

Indexed keywords

ARTICLE; CROHN DISEASE; GENE DELETION; GENE FREQUENCY; GENETIC VARIABILITY; GENOME; GENOME ANALYSIS; HOMO NEANDERTHALENSIS; HUMAN; INTROGRESSION; MOLECULAR EVOLUTION; NONHUMAN; PSORIASIS; PURIFYING SELECTION; ALLELE; ANIMAL; GENETIC VARIATION; GENETICS; HOMINID;

HOMINIDAE;

ALLELES; ANIMALS; EVOLUTION, MOLECULAR; GENETIC VARIATION; GENOME; HOMINIDAE; HUMANS; SEQUENCE DELETION;

EID: 84988268716     PISSN: 07374038     EISSN: 15371719     Source Type: Journal    
DOI: 10.1093/molbev/msu405     Document Type: Article

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