Improved Imputation Accuracy of Rare and Low-Frequency Genetic Variants Using Population-Specific High-Coverage Whole-Genome Sequencing Data Based Imputation Reference Panel

著录项

• 来源
  《Human Heredity》 |2016年第4期|共1页
• 作者

  Mitt Mario; Kals Mart; Parn Kalle; Gabriel Stacey B.; Lander Eric S.; Palotie Aarno; Ripatti Samuli; Morris Andrew P.; Metspalu Andres; Esko Tonu; Magi Reedik; Palta Priit;

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• 作者单位

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

  Broad Inst MIT &

  Harvard Cambridge MA USA;

  Broad Inst MIT &

  Harvard Cambridge MA USA;

  Univ Helsinki Inst Mol Med Finland FIMM Helsinki Finland;

  Univ Helsinki Inst Mol Med Finland FIMM Helsinki Finland;

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

  Univ Tartu Estonian Genome Ctr Tartu Estonia;

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• 收录信息
• 原文格式 PDF
• 正文语种 eng
• 中图分类 医学遗传学;
• 关键词