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. 2021 Jan 29;4:116. doi: 10.1038/s42003-020-01639-0

Table 1.

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

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

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.