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Table 1 Basic statistics produced by SA_Run2Ref for two sequencing run datasets.

From: SeqAssist: a novel toolkit for preliminary analysis of next-generation sequencing data

Illumina MiSeq runs (read length = 2 × 151 bp)

ECT

ECT_rerun

ECT + ECT_rerun

Total number of raw paired-end reads

7,575,822

7,064,035

14,639,857

Total number of cleaned reads

7,524,261

7,041,454

14,565,715

Total number of reads mapped to reference genome

6,573,572

6,193,164

12,766,736

Mapped/Cleaned reads (%)

87.37

87.95

87.65

Total number of scaffolds in reference genome

5,191

5,191

5,191

Number of covered reference scaffolds

3,960

3,948

3,998

Covered/Total scaffolds (%)

76.29

76.05

77.02

Genome coverage breadth (%)

64.48

64.32

66.12

Genome coverage depth

9.24

8.67

17.91

standard deviation of scaffold coverage depth

96.11

91.88

186.95

average scaffold coverage depth

16.27

15.41

31.33

Genome coverage evenness

6.79

6.86

6.82

Run time (min)

44.6

42.0

81.9

  1. The two datasets of paired-end reads were generated using Illumina MiSeq by sequencing the same genomic DNA (gDNA) library prepared for a water flea (Daphnia pulex) from an ECT population. Library preparation involved shearing of extracted gDNA using a Covaris M220 focused-ultrasonicator (Woburn, MA). The average of library insert size distribution was 301 bp.