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Evaluation of genetic variation among Brazilian soybean cultivars through genome resequencing. Repositório Alice
SANTOS, J. V. M. dos; VALLIYODAN, B.; JOSHI, T.; KHAN, S. M.; LIU, YANG.; WANG, J.; VUONG, T. D.; OLIVEIRA, M. F. de; MARCELINO-GUIMARÃES, F. C.; XU, D.; NGUYEN, H. T.; ABDELNOOR, R. V..
Soybean [Glycine max (L.) Merrill] is one of the most important legumes cultivated worldwide, and Brazil is one of the main producers of this crop. Since the sequencing of its reference genome, interest in structural and allelic variations of cultivated and wild soybean germplasm has grown. To investigate the genetics of the Brazilian soybean germplasm, we selected soybean cultivars based on the year of commercialization, geographical region and maturity group and resequenced their genomes. We resequenced the genomes of 28 Brazilian soybean cultivars with an average genome coverage of 14.8X. A total of 5,835,185 single nucleotide polymorphisms (SNPs) and 1,329,844 InDels were identified across the 20 soybean chromosomes, with 541,762 SNPs, 98,922 InDels...
Tipo: Artigo em periódico indexado (ALICE) Palavras-chave: Soja; Variedade; Genoma; Variação genética; Soybeans; Cultivars; High-throughput nucleotide sequencing; Genetic variation.
Ano: 2016 URL: http://www.alice.cnptia.embrapa.br/handle/doc/1037089
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Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits. Repositório Alice
SILVA, J. M. da; GIACHETTO, P. F.; SILVA, L. O. da; CINTRA, L. C.; PAIVA, S. R.; YAMAGISHI, M. E. B.; CAETANO, A. R..
Background: Copy number variations (CNVs) have been shown to account for substantial portions of observed genomic variation and have been associated with qualitative and quantitative traits and the onset of disease in a number of species. Information from high-resolution studies to detect, characterize and estimate population-specific variant frequencies will facilitate the incorporation of CNVs in genomic studies to identify genes affecting traits of importance. Results: Genome-wide CNVs were detected in high-density single nucleotide polymorphism (SNP) genotyping data from 1,717 Nelore (Bos indicus) cattle, and in NGS data from eight key ancestral bulls. A total of 68,007 and 12,786 distinct CNVs were observed, respectively. Cross-comparisons of results...
Tipo: Artigo em periódico indexado (ALICE) Palavras-chave: Bioinformática; Polimorfismo de nucleotídeo único; Genotipagem; Copy number variations; SNP genotyping; Gado de corte; Bioinformatics; Beef cattle; Single nucleotide polymorphism; High-throughput nucleotide sequencing; Genotyping.
Ano: 2016 URL: http://www.alice.cnptia.embrapa.br/handle/doc/1047683
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