Deep sequencing of 10,000 human genomes

Proceedings of the National Academy of Sciences of the United States of America

Volumn 113, Issue 42, 2016, Pages 11901-11906

  Telenti, Amalio ^a,b   Pierce, Levi C T ^a   Biggs, William H ^a   Di Iulio, Julia ^a,b   Wong, Emily H M ^a   Fabani, Martin M ^a   Kirkness, Ewen F ^a   Moustafa, Ahmed ^a   Shah, Naisha ^a   Xie, Chao ^a   Brewerton, Suzanne C ^a   Bulsara, Nadeem ^a   Garner, Chad ^a   Metzker, Gary ^a   Sandoval, Efren ^a   Perkins, Brad A ^a   Och, Franz J ^a   Turpaz, Yaron ^a   Venter, J Craig ^a,b  

^a Human Longevity Inc   (United States)

^b J CRAIG VENTER INSTITUTE   (United States)

Author keywords

Genomics; Human genetic diversity; Noncoding genome

Indexed keywords

ARTICLE; EXON; GENE LOCATION; GENE SEQUENCE; GENETIC CODE; GENETIC VARIABILITY; GENETIC VARIATION; GENOME ANALYSIS; HUMAN; HUMAN GENOME; PATHOGENICITY; PRIORITY JOURNAL; QUALITY CONTROL; REPRODUCIBILITY; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; BIOLOGY; CHROMOSOMAL MAPPING; GENETIC PREDISPOSITION; GENOMICS; NUCLEIC ACID DATABASE; OPEN READING FRAME; PROCEDURES; UNTRANSLATED REGION; WHOLE GENOME SEQUENCING;

CHROMOSOME MAPPING; COMPUTATIONAL BIOLOGY; DATABASES, NUCLEIC ACID; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME, HUMAN; GENOMICS; HUMANS; OPEN READING FRAMES; POLYMORPHISM, SINGLE NUCLEOTIDE; REPRODUCIBILITY OF RESULTS; UNTRANSLATED REGIONS; WHOLE GENOME SEQUENCING;

EID: 84991628639     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1613365113     Document Type: Article

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