Alignment Results

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문서 역사
  1. Number of mapped reads: 543,920,665
  2. Mapped bases: 20,668,985,270bp (20.7 Giga base)
  3. Mapping coverage
    1. Coverage depth: 6.66 X
    2. Reference genome coverage:  98.35 %
  4. Genome coverage and accuracy of SNP detection by sequencing depth]]

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