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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
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BMC Genomics

ISSN: 1471-2164

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