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Table 1 Summary of bases distribution for five samples whole-exome sequencing data

From: Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data

Coverage Sample Total mapped bases (Gb) (%) Mean mapped
depth (×)
Bases accessed(Gb)
(% of genome regions)
High
(Inside target)
1 3.71 (43.7%) 60.53 0.61(98.8%)
  2 3.75 (43.7%) 61.11  
  3 3.88 (43.5%) 63.27  
  4 3.90 (42.7%) 63.57  
  5 3.85 (43.4%) 62.71  
Medium
(outside≤200 bp)
1 1.84 (21.7%) 30.05 0.74(92.1%)
  2 1.85 (21.5%) 30.15  
  3 1.91 (21.4%) 31.14  
  4 1.93 (21.1%) 31.40  
  5 1.89 (21.3%) 30.82  
Low
(outside > 200 bp)
1 2.94 (34.6%) 3.99 1.66 (58.3%)
  2 2.99 (34.8%) 4.03  
  3 3.12 (35.1%) 4.18  
  4 3.30 (36.2%) 4.31  
  5 3.13 (35.3%) 4.16