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Table 3 Summary of sequence assembly after Illumina sequencing

From: Fine mapping and RNA-Seq unravels candidate genes for a major QTL controlling multiple fiber quality traits at the T1 region in upland cotton

Sample name

Raw reads

Clean reads

Clean bases

Error rate (%)

Q20 (%)

Q30 (%)

GC content (%)

R118_0

10144830

9985483

0.5G

0.01

97.94

94.16

43.74

Yumian 1_0

11213370

11081107

0.55G

0.01

98.01

94.35

43.77

R118_5

14141978

14104947

0.71G

0.01

99.03

96.58

44.01

Yumian 1_5

14027353

13969205

0.7G

0.01

98.99

96.49

43.94

  1. Raw reads: Statistical data for the original sequences. Clean reads: Calculation method is the same as for raw reads, but the statistics file is the filtered data. Clean bases:sequence number*sequence length (transformed into G bases). Q20、Q30:Percentage of the number of bases of Phred score greater than 20, 30 respectively. GC content:Percentage of G and C bases among the total base number