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机译:全基因组定位和小鼠基因组结构变异断点的组装
Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA;
Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA;
Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA;
Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA;
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom;
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, United Kingdom;
Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 3Z4, Canada;
Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA|Center for Public Health Genomics, University of Virginia, Charlottesville, Virginia 22908, USA;
机译:全基因组定位和小鼠基因组中结构变异断点的组装。
机译:De Novo基因组组装汉族雄性和基因组宽检测结构变体使用牛津纳米孔测序
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机译:SCJ:各种分界点距离,可以轻松解决排序,基因组中位数和基因组减半问题
机译:断点接近鉴定的编码和非分量癌驱动程序的结构变体及表达分析
机译:全基因组定位和小鼠基因组结构变异断点的组装
机译:全基因组定位和小鼠基因组结构变异断点的组装