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Table 1 Sequencing coverage

From: Coupling high-throughput genetics with phylogenetic information reveals an epistatic interaction on the influenza A virus M segment

Replicate Library type Average Minimum Maximum
   coverage coverage coverage
DNA input Whole segment 157,846 82,998 189,371
DNA input Small libraries 54,850 44,297 105,183
1 Whole segment 242,390 158,210 276,850
2 Whole segment 43,286 11,451 131,578
3 Small libraries 59,694 30,003 113,619
4 Small libraries 50,758 29,606 91,134
5 Small libraries 63,659 18,201 104,731
  1. For those replicates with the library type indicated as “Whole Segment”, the coverage represents the number of error-corrected reads [19]. For those replicates with the library type indicated as “Small Libraries”, the coverage represents the number of sequencing reads