Table 1 Data obtained from Oxford Nanopore runs both mined and retrieved mitochondrial DNA (see text for protocol information).

From: Evidence of two deeply divergent co-existing mitochondrial genomes in the Tuatara reveals an extremely complex genomic organization

Run

Modification to library preparation

Chemistry

Total # of reads (K)

Total yield (Gb)

mt-reads >500 bp

mtDNA yield (kb)

Mapped molecule 1 mt-reads

Mapped molecule 1 yield (kb)

Mapped molecule 2 mt-reads

Mapped molecule 2 yield (kb)

1

10 kb shear

1D, R9.4, SQK-108

165.43

0.99

7

25.31

7

25.31

0

0

2

10 kb shear, Trypsin

1D, R9.4, SQK-108

353.58

2.06

16

94.42

9

43.87

5

24.54

3

2D

2D, R9.4, SQK-208

18.79

0.26

10

27.83

9

45.02

0

0

4

5 kb shear

1D, R9.4, SQK-108

34.64

0.31

0

0

0

0

0

0

5

Trypsin

1D, R9.4, SQK-208

265.17

0.98

8

46.46

6

14.16

1

4.836

6

Trypsin

1D, R9.4, SQK-108

18.31

0.11

1

3.43

1

3.39

0

0

7

Trypsin

1D, R9.4, LSK109

1224.00

1.30

36

74.99

31

64.60

4

8.22

8

Trypsin

1D, R9.4, LSK109

5149.57

3.45

80

112.71

51

74.69

22

26.09

Totals

 

7229.48

9.46

158

385.15

114

271.04

32

63.69

  1. Run numbers are described in the text: library preparation methods refer to variations in protocols described in the methods section, chemistry is the type of sequencing run and the version of flow cell used. Run numbers 1–3 are SRA run numbers 1–3, run number 4 is SRA run number 5, run number 5 is SRA run number 6, run number 6 is SRA run number 10, run number 7 is SRA run number 14, and run number 8 is SRA run number 15.