Genetic variation in an individual human exome

• المؤلفون الرئيسيون: Ng P.C., Levy S., Huang J., Stockwell T.B., Walenz B.P., Li K., Axelrod N., Busam D.A., Strausberg R.L., Venter J.C.
• مؤلفون آخرون: MEDICINE
• التنسيق: مقال
• منشور في: 2019
• الموضوعات: amino acid; protein; article; bioinformatics; exon; gene; gene deletion; gene insertion; genetic variability; genome; genomics; human; protein function; single nucleotide polymorphism; comparative study; gene frequency; genetic disorder; genetics; male; metabolism; mutation; phenotype; Exons; Gene Frequency; Genetic Diseases, Inborn; Genome, Human; Humans; Male; Mutation; Phenotype; Polymorphism, Single Nucleotide; Proteins; Variation (Genetics)
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/161684

10.1371/journal.pgen.1000160