Variant calling in low-coverage whole genome sequencing of a Native American population sample - Bizon, Chris; Spiegel, Michael; Chasse, Scott A; Gizer, Ian R; Li, Yun; Malc, Ewa P; Mieczkowski, Piotr A; Sailsbery, Josh K; Wang, Xiaoshu; Ehlers, Cindy L; Wilhelmsen, Kirk C (BMC genomics, 2014)
Keywords: Adolescent; Adult; Aged; Aged, 80 and over; Analysis; Animal Genetics and Genomics; Arrays; Association analysis; Biomedical and Life Sciences; Cohort Studies; DNA sequencing; Exome; Gene Frequency; Genetic aspects; Genetic Variation; Genome, Human; Genomes; Genomics; Genotype; Genotypes; Haplotypes; High-Throughput Nucleotide Sequencing; Human and rodent genomics; Humans; Indians, North American - genetics; Indigenous peoples; Life Sciences; Linkage Disequilibrium; Microarrays; Microbial Genetics and Genomics; Middle Aged; Nucleotide sequencing; Oligonucleotide Array Sequence Analysis; Plant Genetics and Genomics; Polymorphism, Single Nucleotide; Proteomics; Research Article; Software; Studies; Young Adult; Whole Genome Sequencing Data; Variant Calling; Variant Call; Whole Genome Sequencing; Kinship Coefficient