Skip to main content

Table 2 Summary of the target detection module outputs from Khan et al.’s dataset analysis.

From: Entourage: all-in-one sequence analysis software for genome assembly, virus detection, virus discovery, and intrasample variation profiling

Virus

Overall sequencing depth ( ×)†

# of contigs

Contig lengths (bases)

Contig supporting reads

Contig sequencing depths ( ×)

% identities against target reference best hits

3 × sample

EBV

16.22

7

2349–42,533

495–6558

15.53–105.03

99.25–100.00

RSV

57.59

1

15,407

8673

55.80

99.97

FeLV

6.21

3

649–4093

56–357

8.37–8.72

97.17–100.00

REO1 (11 segments)

51.98* (8.49–77.90)

11

407–3920

19–2697

4.69–77.83

93.64–100.00

HPV18

3,651.84

3

1053–2761

2130–144,366

201.84–5782.25

99.96–100.00

0.1 × sample

EBV

0.45

3

427- 977

12–44

2.80–5.21

100.00–100.00

RSV

4.38

7

407–1176

13–180

3.23–17.93

99.77–100.00

FeLV

0.55

–

–

–

–

–

REO1 (11 segments)

0.47* (0.05–0.82)

–

–

–

–

–

HPV18

7,888.71

2

1262–5868

7514–402,649

596.71–6844.17

99.96–100.00

  1. See Supplementary File 1 for raw outputs
  2. *length weighted average. See sequencing depth of each individual segment in Table S3
  3. †estimated mapping clean non-human / non-phiX174 reads against selected reference sequences (Table S3)