Comprehensive Characterization of Human Genome Variation by High Coverage Whole-Genome Sequencing of Forty Four Caucasians

• Main Authors: Shen H., Li J., Zhang J., Xu C., Jiang Y., Wu Z., Zhao F., Liao L., Chen J., Lin Y., Tian Q., Papasian C.J., Deng H.-W.
• Other Authors: MICROBIOLOGY AND IMMUNOLOGY
• Format: Article
• Published: 2019
• Subjects: adult; article; Caucasian; female; gene deletion; gene frequency; gene inactivation; gene insertion; gene product; genetic procedures; genetic variability; high coverage whole genome sequencing; homozygosity; human; loss of function mutation; male; nucleic acid base substitution; single nucleotide polymorphism; Adult; Chromosomes, Human, Y; Disease; DNA Copy Number Variations; DNA, Mitochondrial; European Continental Ancestry Group; Female; Genome, Human; Genomics; Humans; INDEL Mutation; Male; Mutation Rate; Polymorphism, Single Nucleotide; Sequence Analysis, DNA
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/161331
• Institution: National University of Singapore

10.1371/journal.pone.0059494